MONDO:0002974	cervical cancer
MONDO:0000311	congenital hypothyroidism
MONDO:0000310	Alkhurma hemorrhagic fever
MONDO:0002975	malignant breast melanoma
MONDO:0002976	stomach diverticulosis
MONDO:0002977	autoimmune disease of the nervous system
MONDO:0000315	commensal bacterial infectious disease
MONDO:0002970	ciliary body disease
MONDO:0002971	amelanotic melanoma
MONDO:0000314	primary bacterial infectious disease
MONDO:0000313	hypophosphatemia
MONDO:0002972	posterior mediastinum cancer
MONDO:0002973	epithelioid cell melanoma
MONDO:0000312	enlarged vestibular aqueduct
MONDO:0014959	mitochondrial DNA depletion syndrome 12A (cardiomyopathic type), autosomal dominant
MONDO:0014958	Harel-Yoon syndrome
MONDO:0014957	language delay and attention deficit-hyperactivity disorder/cognitive impairment with or without cardiac arrhythmia
MONDO:0014963	Shashi-Pena syndrome
MONDO:0012300	prostate cancer, hereditary, 6
MONDO:0012301	mitochondrial DNA depletion syndrome, myopathic form
MONDO:0014962	intellectual disability, autosomal recessive 57
MONDO:0014961	spermatogenic failure 16
MONDO:0014960	encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy
MONDO:0014967	heterotaxy, visceral, 8, autosomal
MONDO:0012304	photoparoxysmal response 2
MONDO:0012305	photoparoxysmal response 3
MONDO:0014966	periventricular nodular heterotopia 7
MONDO:0014965	lethal congenital contracture syndrome 11
MONDO:0012302	parietal foramina 3
MONDO:0012303	migraine with or without aura, susceptibility to, 8
MONDO:0014964	encephalopathy, progressive, early-onset, with brain atrophy and thin corpus callosum
MONDO:0000308	primary systemic mycosis
MONDO:0000307	parasitic Ichthyosporea infectious disease
MONDO:0000306	trichosporonosis
MONDO:0000305	fusariosis
MONDO:0002967	dermatophytosis of scalp or beard
MONDO:0002968	lymphocele
MONDO:0002969	ciliary body cancer
MONDO:0000309	aniseikonia
MONDO:0000322	Carrion disease
MONDO:0002985	pustulosis of palm and sole
MONDO:0000321	typhoidal tularemia
MONDO:0002986	neuromuscular disease
MONDO:0000320	glandular tularemia
MONDO:0002987	spongiotic dermatitis
MONDO:0002988	cervix melanoma
MONDO:0002981	peripheral primitive neuroectodermal tumor of bone
MONDO:0000326	lissencephaly
MONDO:0002982	peripheral primitive neuroectodermal tumor of soft tissues
MONDO:0000325	pachyonychia congenita
MONDO:0002983	neuromuscular junction disease
MONDO:0000324	familial partial lipodystrophy
MONDO:0002984	reticulohistiocytic granuloma
MONDO:0000323	familial adenomatous polyposis
MONDO:0014949	developmental and epileptic encephalopathy, 47
MONDO:0014948	short stature, rhizomelic, with microcephaly, micrognathia, and developmental delay
MONDO:0014947	developmental and epileptic encephalopathy, 46
MONDO:0014946	Sifrim-Hitz-Weiss syndrome
MONDO:0002980	myofibroma
MONDO:0014952	intellectual disability-epilepsy-extrapyramidal syndrome
MONDO:0014951	Sotos syndrome 3
MONDO:0014950	aortic aneurysm, familial thoracic 10
MONDO:0014956	Chitayat syndrome
MONDO:0014955	retinal dystrophy with or without extraocular anomalies
MONDO:0014954	Ehlers-Danlos syndrome, periodontal type 2
MONDO:0014953	gnb5-related intellectual disability-cardiac arrhythmia syndrome
MONDO:0000319	infant botulism
MONDO:0000318	wound botulism
MONDO:0000317	foodborne botulism
MONDO:0000316	opportunistic bacterial infectious disease
MONDO:0002978	orbit alveolar rhabdomyosarcoma
MONDO:0002979	papillary squamous carcinoma
MONDO:0002952	follicular basal cell carcinoma
MONDO:0002953	skin infiltrative basal cell carcinoma
MONDO:0002954	superficial multifocal basal cell carcinoma
MONDO:0002955	vulva basal cell carcinoma
MONDO:0002950	skin clear cell basal cell carcinoma
MONDO:0002951	skin adenoid basal cell carcinoma
MONDO:0014938	aniridia 3
MONDO:0014937	aniridia 2
MONDO:0014936	ZTTK syndrome
MONDO:0014935	frontometaphyseal dysplasia 2
MONDO:0014939	congenital myasthenic syndrome 20
MONDO:0014941	arthrogryposis, distal, with impaired proprioception and touch
MONDO:0014940	neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset
MONDO:0014945	myopathy, distal, with rimmed vacuoles
MONDO:0014944	short stature-brachydactyly-obesity-global developmental delay syndrome
MONDO:0014943	mitochondrial DNA depletion syndrome 15 (hepatocerebral type);
MONDO:0014942	developmental and epileptic encephalopathy, 45
MONDO:0002949	morpheaform basal cell carcinoma
MONDO:0002945	micronodular basal cell carcinoma
MONDO:0002946	gynatresia
MONDO:0002947	adamantinoid basal cell epithelioma
MONDO:0002948	skin fibroepithelial basal cell carcinoma
MONDO:0002963	acantholytic acanthoma
MONDO:0000300	tungiasis
MONDO:0002964	non-Langerhans-cell histiocytosis
MONDO:0002965	parovarian cyst
MONDO:0002966	splenic manifestation of prolymphocytic leukemia
MONDO:0000304	penicilliosis
MONDO:0002960	polyradiculopathy
MONDO:0000303	conidiobolomycosis
MONDO:0000302	basidiobolomycosis
MONDO:0002961	large cell acanthoma
MONDO:0002962	epidermolytic acanthoma
MONDO:0000301	ophthalmomyiasis
MONDO:0014927	Joubert syndrome 27
MONDO:0014926	Bardet-Biedl syndrome 22
MONDO:0014925	epilepsy, familial focal, with variable foci 3
MONDO:0014924	epilepsy, familial focal, with variable foci 2
MONDO:0014929	retinitis pigmentosa 76
MONDO:0014928	Joubert syndrome 28
MONDO:0014930	intellectual disability, autosomal recessive 56
MONDO:0014934	spinocerebellar ataxia, autosomal recessive 24
MONDO:0014933	developmental and epileptic encephalopathy, 44
MONDO:0014932	orofaciodigital syndrome XV
MONDO:0014931	Alazami-Yuan syndrome
MONDO:0002956	skin cystic basal cell carcinoma
MONDO:0002957	sarcomatoid basal cell carcinoma
MONDO:0002958	signet ring basal cell carcinoma
MONDO:0002959	radiculopathy
MONDO:0000355	Ullrich congenital muscular dystrophy
MONDO:0024322	disorder of glycosylation
MONDO:0000354	JMP syndrome
MONDO:0024321	disorder of GPI anchor biosynthesis
MONDO:0000353	Saldino-Noonan syndrome
MONDO:0024323	glomangiomyoma
MONDO:0000352	hereditary sensory neuropathy
MONDO:0024326	pleural adenomatoid tumor
MONDO:0000359	spondylocostal dysostosis
MONDO:0000358	orofacial cleft
MONDO:0024325	cutaneous glomangiomyoma
MONDO:0000357	West syndrome
MONDO:0024327	chronic renal failure syndrome
MONDO:0000356	Walker-Warburg syndrome
MONDO:0012339	celiac disease, susceptibility to, 4
MONDO:0000351	disorder of methionine catabolism
MONDO:0000350	Charcot-Marie-Tooth disease intermediate type
MONDO:0024320	inner ear neoplasm
MONDO:0012344	Alzheimer disease 11
MONDO:0012345	acral peeling skin syndrome
MONDO:0012342	7q11.23 microduplication syndrome
MONDO:0012343	aortic aneurysm, familial abdominal, 2
MONDO:0012348	maturity-onset diabetes of the young type 8
MONDO:0012349	spondylocostal dysostosis 3, autosomal recessive
MONDO:0012346	generalized epilepsy with febrile seizures plus, type 4
MONDO:0012347	hamartoma, Precalcaneal congenital fibrolipomatous
MONDO:0024318	viral infection of central nervous system
MONDO:0000349	Charcot-Marie-Tooth disease type 1
MONDO:0012340	celiac disease, susceptibility to, 2
MONDO:0012341	celiac disease, susceptibility to, 3
MONDO:0000366	glycogen storage disease IX
MONDO:0024311	cancer affecting bone of limb skeleton
MONDO:0000365	primary congenital glaucoma
MONDO:0024310	angiodysplasia of stomach
MONDO:0024313	staphylococcal infection
MONDO:0000364	severe congenital neutropenia
MONDO:0000363	gummatous syphilis
MONDO:0024312	cancer of short bone of upper limb
MONDO:0024315	parasitic endophthalmitis
MONDO:0024314	parasitemia
MONDO:0000369	abdominal tuberculosis
MONDO:0000368	extrapulmonary tuberculosis
MONDO:0024317	chronic pain syndrome
MONDO:0024316	physiological malfunction arising from mental factor
MONDO:0000367	taeniasis
MONDO:0012328	trichilemmal cyst
MONDO:0012329	short stature and Facioauriculothoracic malformations
MONDO:0000362	Sensenbrenner syndrome
MONDO:0000361	d-2-hydroxyglutaric aciduria
MONDO:0000360	2-hydroxyglutaric aciduria
MONDO:0012333	autosomal recessive nonsyndromic deafness 53
MONDO:0014996	intellectual disability, autosomal recessive 58
MONDO:0012334	hereditary spastic paraplegia 29
MONDO:0014995	neurodevelopmental disorder with hypotonia, seizures, and absent language
MONDO:0014994	global developmental delay, absent or hypoplastic corpus callosum, and dysmorphic facies
MONDO:0012331	migraine with aura, susceptibility to, 9
MONDO:0014993	myofibrillar myopathy 8
MONDO:0012332	short stature-delayed bone age due to thyroid hormone metabolism deficiency
MONDO:0012337	glaucoma 1, open angle, I
MONDO:0012338	epilepsy, idiopathic generalized, susceptibility to, 4
MONDO:0014999	tooth agenesis, selective, 9
MONDO:0012335	obesity due to pro-opiomelanocortin deficiency
MONDO:0014998	glaucoma 3, primary congenital, E
MONDO:0012336	cataract 22 multiple types
MONDO:0014997	nephronophthisis 20
MONDO:0024308	pseudoxanthoma elasticum (inherited or acquired)
MONDO:0024307	prothrombin deficiency
MONDO:0024309	neuropathy, hereditary sensory and autonomic, type 2A
MONDO:0014992	lissencephaly 8
MONDO:0012330	talo-patello-scaphoid osteolysis
MONDO:0014991	Seckel syndrome 10
MONDO:0014990	uncombable hair syndrome 3
MONDO:0000333	early congenital syphilis
MONDO:0002996	cavernous sinus meningioma
MONDO:0024300	hypophosphatemic rickets
MONDO:0000332	sennetsu fever
MONDO:0002997	anterior cranial fossa meningioma
MONDO:0024302	internal hirudiniasis
MONDO:0000331	Rickettsia helvetica spotted fever
MONDO:0002998	skull base meningioma
MONDO:0000330	endemic typhus
MONDO:0002999	central nervous system germinoma
MONDO:0024301	acquired mineral metabolism disease
MONDO:0000337	exanthema subitum
MONDO:0024304	ichthyosis vulgaris
MONDO:0002992	juvenile xanthogranuloma
MONDO:0024303	external hirudiniasis
MONDO:0002993	pancreatic somatostatinoma
MONDO:0000336	meningovascular neurosyphilis
MONDO:0002994	pancreatic delta cell neuroendocrine tumor
MONDO:0000335	parenchymatous neurosyphilis
MONDO:0024306	acquired lactic acidosis
MONDO:0000334	multinodular goiter
MONDO:0002995	small intestine neuroendocrine tumor, well differentiated, low or intermediate grade
MONDO:0024305	acquired hyperprolactinemia
MONDO:0012319	major affective disorder 3
MONDO:0012317	visceral neuropathy, familial, 3, autosomal dominant
MONDO:0002990	benign deep fibrous histiocytoma
MONDO:0014979	myoclonus, intractable, neonatal
MONDO:0002991	adenocarcinofibroma
MONDO:0012318	leukemia, chronic lymphocytic, susceptibility to, 1
MONDO:0012322	holoprosencephaly 5
MONDO:0014985	Fanconi anemia complementation group V
MONDO:0012323	lethal acantholytic epidermolysis bullosa
MONDO:0014984	lung disease, immunodeficiency, and chromosome breakage syndrome;
MONDO:0012320	migraine, familial hemiplegic, 3
MONDO:0014983	congenital myasthenic syndrome 21
MONDO:0012321	Alzheimer disease 10
MONDO:0014982	myopia 25, autosomal dominant
MONDO:0012326	autosomal recessive nonsyndromic deafness 42
MONDO:0014989	uncombable hair syndrome 2
MONDO:0012327	autosomal recessive nonsyndromic deafness 46
MONDO:0014988	3-methylglutaconic aciduria, type VIII
MONDO:0012324	Frias syndrome
MONDO:0014987	Fanconi anemia complementation group U
MONDO:0012325	Nguyen syndrome
MONDO:0014986	Fanconi anemia complementation group R
MONDO:0000329	epidemic typhus
MONDO:0000328	hyperphosphatemia
MONDO:0000327	Buruli ulcer disease
MONDO:0014981	immunodeficiency 49
MONDO:0002989	benign fibrous histiocytoma
MONDO:0014980	cone-rod dystrophy and hearing loss
MONDO:0000344	Ross river fever
MONDO:0000343	Barmah forest virus disease
MONDO:0000342	O'nyong'nyong fever
MONDO:0000341	paralytic poliomyelitis
MONDO:0000348	posterior polar cataract
MONDO:0000347	adult T-cell leukemia/lymphoma
MONDO:0000346	Hantavirus hemorrhagic fever with renal syndrome, Dobrava-Belgrade virus type
MONDO:0000345	Oropouche fever
MONDO:0012308	Joubert syndrome with renal defect
MONDO:0012309	parietal foramina 2
MONDO:0014969	isolated sedoheptulokinase deficiency
MONDO:0012306	cardiomyopathy, familial restrictive, 2
MONDO:0014968	encephalopathy, progressive, with amyotrophy and optic atrophy
MONDO:0012307	familial scaphocephaly syndrome, McGillivray type
MONDO:0000340	bulbospinal polio
MONDO:0012311	spondylomegaepiphyseal dysplasia with upper limb mesomelia, punctate calcifications, and deafness
MONDO:0014974	sudden cardiac failure, alcohol-induced
MONDO:0012312	short QT syndrome type 1
MONDO:0014973	sudden cardiac failure, infantile
MONDO:0014972	chromosome 19q13.11 deletion syndrome, proximal
MONDO:0014971	amelogenesis imperfecta, hypomaturation type, IIa6
MONDO:0012310	fibrosis of extraocular muscles, congenital, with synergistic divergence
MONDO:0012315	distal 10q deletion syndrome
MONDO:0014978	preimplantation embryonic lethality 2
MONDO:0012316	Majeed syndrome
MONDO:0014977	autosomal recessive limb-girdle muscular dystrophy type 2Z
MONDO:0014976	lethal left ventricular non-compaction-seizures-hypotonia-cataract-developmental delay syndrome
MONDO:0012313	short QT syndrome type 2
MONDO:0014975	autosomal recessive spastic paraplegia type 78
MONDO:0012314	short QT syndrome type 3
MONDO:0000339	spinal polio
MONDO:0000338	variola major infectious disease
MONDO:0014970	spermatogenic failure 17
MONDO:0002900	cerebral neuroblastoma
MONDO:0002930	kidney sarcoma
MONDO:0002931	conjunctivochalasis
MONDO:0002932	conjunctival disease
MONDO:0002933	osteosclerosis
MONDO:0014916	developmental and epileptic encephalopathy, 41
MONDO:0014915	short-rib thoracic dysplasia 16 with or without polydactyly
MONDO:0014914	Dias-Logan syndrome
MONDO:0014919	sessile serrated polyposis cancer syndrome
MONDO:0014918	tall stature-intellectual disability-renal anomalies syndrome
MONDO:0014917	developmental and epileptic encephalopathy, 42
MONDO:0014923	peeling skin syndrome 5
MONDO:0014922	myofibrillar myopathy 7
MONDO:0014921	developmental and epileptic encephalopathy, 43
MONDO:0014920	patterned macular dystrophy 3
MONDO:0600030	B-cell acute lymphoblastic leukemia with t(1;19)(q23;p13.3); E2A-PBX1 (TCF3-PBX1)
MONDO:0002927	spindle cell sarcoma
MONDO:0002928	carcinosarcoma
MONDO:0002929	pulmonary immaturity
MONDO:0002923	uterine corpus endometrial stromal sarcoma
MONDO:0002924	smooth muscle cancer
MONDO:0002925	extraosseous Ewing's sarcoma
MONDO:0002926	clear cell sarcoma
MONDO:0002941	anal margin carcinoma
MONDO:0002942	sebaceous basal cell carcinoma
MONDO:0002943	external ear basal cell carcinoma
MONDO:0002944	external ear carcinoma
MONDO:0002940	anal margin basal cell carcinoma
MONDO:0014905	encephalopathy due to defective mitochondrial and peroxisomal fission 2
MONDO:0014904	congenital disorder of glycosylation, type IAA
MONDO:0014903	seizures, benign familial infantile, 5
MONDO:0014902	nasopharyngeal carcinoma, susceptibility to, 3
MONDO:0014909	primary ciliary dyskinesia 34
MONDO:0014908	microcephaly 17, primary, autosomal recessive
MONDO:0014907	short-rib thoracic dysplasia 15 with polydactyly
MONDO:0014906	Charcot-Marie-Tooth disease, axonal, autosomal recessive, type 2a2b;
MONDO:0014912	infantile-onset periodic fever-panniculitis-dermatosis syndrome
MONDO:0014911	growth retardation, intellectual developmental disorder, hypotonia, and hepatopathy
MONDO:0014910	primary ciliary dyskinesia 35
MONDO:0002938	metatypical basal cell carcinoma
MONDO:0002939	skin pigmented basal cell carcinoma
MONDO:0002934	intravascular angioleiomyoma
MONDO:0002935	penis basal cell carcinoma
MONDO:0002936	scrotum basal cell carcinoma
MONDO:0002937	nodular basal cell carcinoma
MONDO:0002910	peroneal neuropathy
MONDO:0002911	brain stem glioma
MONDO:0014901	tooth agenesis, selective, 8
MONDO:0002909	hyperglycemia
MONDO:0014900	autosomal recessive limb-girdle muscular dystrophy type 2Y
MONDO:0002905	mutism
MONDO:0002906	scleroderma
MONDO:0002907	intracranial thrombosis
MONDO:0002908	glucose metabolism disease
MONDO:0002901	blood group incompatibility
MONDO:0002902	pseudohypoparathyroidism
MONDO:0002903	articulation disorder
MONDO:0002904	echolalia
MONDO:0002920	malignant ovarian Brenner tumor
MONDO:0002921	congenital structural myopathy
MONDO:0002922	pyoderma
MONDO:0002916	brainstem intraparenchymal clear cell meningioma
MONDO:0002917	disease of pilosebaceous unit
MONDO:0002918	clear cell meningioma
MONDO:0002919	posterior cranial fossa meningioma
MONDO:0002912	brainstem cancer
MONDO:0002913	cerebellar neoplasm
MONDO:0002914	childhood brain stem neoplasm
MONDO:0002915	childhood infratentorial neoplasm
MONDO:0600008	cytokine release syndrome
MONDO:0600009	severe hypophosphatasia
MONDO:0600001	glutaminase deficiency
MONDO:0600002	hemorrhagic fever
MONDO:0600003	bacterial hemorrhagic fever
MONDO:0600005	venom allergy
MONDO:0600017	acinar dysplasia caused by mutation in FGF10
MONDO:0600018	acinar dysplasia caused by mutation in FGFR2
MONDO:0600019	acinar dysplasia caused by mutation in TBX4
MONDO:0600010	moderate hypophosphatasia
MONDO:0600011	mild hypophosphatasia
MONDO:0600014	alveolar capillary dysplasia without misalignment of pulmonary veins
MONDO:0600016	acinar dysplasia
MONDO:0600029	restrictive pulmonary disease
MONDO:0600023	idiopathic inflammatory myopathy
MONDO:0600024	familial idiopathic inflammatory myopathy
MONDO:0600025	hydrosalpinx
MONDO:0600026	vanishing lung syndrome
MONDO:0600027	congenital right-sided heart lesions
MONDO:0000399	dyskinetic cerebral palsy
MONDO:0000398	female breast cancer
MONDO:0000397	ataxic cerebral palsy
MONDO:0000396	spastic cerebral palsy
MONDO:0000391	Bethlem myopathy
MONDO:0000390	vitelliform macular dystrophy
MONDO:0024360	central sleep apnea caused by high altitude
MONDO:0000395	alcohol-related birth defect
MONDO:0024361	circadian rhythm sleep disorder
MONDO:0000394	alcohol-related neurodevelopmental disorder
MONDO:0000393	partial fetal alcohol syndrome
MONDO:0024363	rapid eye movement sleep disorder
MONDO:0000392	fetal alcohol syndrome
MONDO:0012388	myopia 11, autosomal dominant
MONDO:0012389	myopia 12, autosomal dominant
MONDO:0012386	trichoscyphodysplasia
MONDO:0012387	osteosclerosis-ichthyosis-premature ovarian failure syndrome
MONDO:0012380	autosomal dominant nonsyndromic deafness 53
MONDO:0012381	hyperinsulinism due to INSR deficiency
MONDO:0012384	panic disorder 3
MONDO:0012385	metaphyseal chondrodysplasia with cone-shaped epiphyses, normal hair, and normal hands
MONDO:0012382	hyperinsulinemic hypoglycemia, familial, 4
MONDO:0012383	primary immunodeficiency with natural-killer cell deficiency and adrenal insufficiency
MONDO:0024355	respiratory tract infectious disease
MONDO:0024354	cytomegalovirus pneumonia
MONDO:0024357	drug induced central sleep apnea
MONDO:0024356	primary central sleep apnea syndrome
MONDO:0024359	central sleep apnea due to periodic breathing
MONDO:0024358	complex sleep apnea
MONDO:0024351	familial pityriasis rubra pilaris
MONDO:0024350	pityriasis steatoides
MONDO:0024352	viral respiratory tract infection
MONDO:0012377	asperger syndrome, susceptibility to, 4
MONDO:0012378	fibromatosis, gingival, 3
MONDO:0012375	autosomal recessive nonsyndromic deafness 47
MONDO:0012376	autosomal recessive nonsyndromic deafness 55
MONDO:0012379	asthma-related traits, susceptibility to, 3
MONDO:0012370	autosomal recessive nonsyndromic deafness 51
MONDO:0012373	ectodermal dysplasia, sensorineural hearing loss, and distinctive facial features
MONDO:0012374	brachyphalangy, polydactyly, and tibial aplasia/hypoplasia
MONDO:0012371	Noonan syndrome 3
MONDO:0012372	hypertrichosis, hyperkeratosis, mental retardation, and distinctive facial features
MONDO:0024344	pityriasis folliculorum
MONDO:0000377	malignant Leydig cell tumor
MONDO:0024343	pityriasis simplex
MONDO:0000376	respiratory system cancer
MONDO:0000375	bronchus carcinoma in situ
MONDO:0024346	pityriasis amiantacea
MONDO:0024345	pityriasis streptogenes
MONDO:0000374	bile duct carcinoma in situ
MONDO:0024348	pityriasis capitis
MONDO:0000379	malignant Sertoli-Leydig cell tumor
MONDO:0000378	malignant Sertoli cell tumor
MONDO:0024349	pityriasis alba
MONDO:0024340	retinal neuroblastoma
MONDO:0000373	gall bladder carcinoma in situ
MONDO:0000372	pharynx carcinoma in situ
MONDO:0000371	oral cavity carcinoma in situ
MONDO:0024341	retinal cell neoplasm
MONDO:0000370	Askin's tumor
MONDO:0012366	gallbladder disease 3
MONDO:0012367	retinitis pigmentosa 31
MONDO:0012364	dilated cardiomyopathy 1Q
MONDO:0012365	gallbladder disease 2
MONDO:0012368	aminoacylase 1 deficiency
MONDO:0012369	systemic lupus erythematosus, susceptibility to, 6
MONDO:0012362	dilated cardiomyopathy 1P
MONDO:0012363	retinitis pigmentosa 32
MONDO:0012360	congenital nongoitrous hypothryoidism 3
MONDO:0012361	systemic lupus erythematosus, susceptibility to, 5
MONDO:0024333	sciatica
MONDO:0000388	anonychia congenita
MONDO:0000387	hypochromic microcytic anemia
MONDO:0024332	perennial allergic rhinitis
MONDO:0000386	digestive system neuroendocrine tumor, grade 1/2
MONDO:0024335	retrobulbar neuritis
MONDO:0000385	benign digestive system neoplasm
MONDO:0024334	peripheral nerve lesion
MONDO:0024337	urothelial neoplasm
MONDO:0024336	vulvar adenocarcinoma
MONDO:0024339	lymph node neoplasm
MONDO:0000389	atelosteogenesis
MONDO:0024338	mucinous neoplasm
MONDO:0000380	paranasal sinus carcinoma
MONDO:0000384	bladder benign neoplasm
MONDO:0000383	benign reproductive system neoplasm
MONDO:0024331	colorectal carcinoma
MONDO:0000382	respiratory system benign neoplasm
MONDO:0024330	infectious otitis media
MONDO:0000381	infiltrating renal pelvis transitional cell carcinoma
MONDO:0012355	autosomal recessive nonsyndromic deafness 28
MONDO:0012356	glomerulocystic kidney disease with hyperuricemia and isosthenuria
MONDO:0012353	erythrocytosis, familial, 3
MONDO:0012354	platelet-type bleeding disorder 8
MONDO:0012359	combined immunodeficiency due to partial RAG1 deficiency
MONDO:0012357	glaucoma 1, open angle, G
MONDO:0012358	leprosy, susceptibility to, 1
MONDO:0012351	zygodactyly type 1
MONDO:0012352	vasculitis, lymphocytic, cutaneous small vessel
MONDO:0012350	complement factor H deficiency
MONDO:0024390	actinomycotic infectious disease
MONDO:0024392	anaerobic balanitis
MONDO:0024388	Clostridium infectious disease
MONDO:0024387	benign ovarian sex cord-stromal tumor
MONDO:0024389	anaerobic bacteria infectious disease
MONDO:0024382	circadian rhythm sleep disorder, shift work type
MONDO:0024381	circadian rhythm sleep disorder, jet lag type
MONDO:0024386	large cell lung carcinoma, clear cell variant
MONDO:0024385	arenavirus infectious disease
MONDO:0024377	circadian rhythm sleep disorder, delayed sleep phase type
MONDO:0024376	sleep disorder, initiating and maintaining sleep
MONDO:0024379	circadian rhythm sleep disorder, irregular sleep wake type
MONDO:0024378	circadian rhythm sleep disorder, advanced sleep phase type
MONDO:0012399	complex cortical dysplasia with other brain malformations 7
MONDO:0012397	brachydactyly, coloboma, and anterior segment dysgenesis
MONDO:0012398	retinal cone dystrophy 3A
MONDO:0012391	neuronal ceroid lipofuscinosis 8 northern epilepsy variant
MONDO:0012392	2-methylbutyryl-CoA dehydrogenase deficiency
MONDO:0012390	arthrogryposis multiplex with deafness, inguinal hernias, and early death
MONDO:0012395	cataract 18
MONDO:0012396	exercise-induced hyperinsulinism
MONDO:0012393	congenital brain dysgenesis due to glutamine synthetase deficiency
MONDO:0012394	multiple synostoses syndrome 2
MONDO:0002853	rectum rhabdomyosarcoma
MONDO:0002854	prostate sarcoma
MONDO:0002855	ectomesenchymoma
MONDO:0002856	gallbladder rhabdomyosarcoma
MONDO:0002850	central nervous system rhabdomyosarcoma
MONDO:0002851	mediastinum rhabdomyosarcoma
MONDO:0002852	mediastinum sarcoma
MONDO:0014839	chorea, childhood-onset, with psychomotor retardation
MONDO:0014838	Coffin-Siris syndrome 5
MONDO:0014837	thrombocytopenia 6
MONDO:0014836	Charcot-Marie-Tooth disease axonal type 2CC
MONDO:0014842	intellectual disability, autosomal dominant 41
MONDO:0014841	trichothiodystrophy 6, nonphotosensitive
MONDO:0014840	agammaglobulinemia 8, autosomal dominant
MONDO:0014846	autosomal recessive cerebellar ataxia - epilepsy - intellectual disability syndrome due to TUD deficiency
MONDO:0014845	spinocerebellar ataxia, autosomal recessive 22
MONDO:0014844	premature ovarian failure 12
MONDO:0014843	premature ovarian failure 11
MONDO:0002846	granulomatous gastritis
MONDO:0002847	skeletal muscle cancer
MONDO:0002848	skeletal muscle neoplasm
MONDO:0002849	liver rhabdomyosarcoma
MONDO:0002864	anus rhabdomyosarcoma
MONDO:0000201	thyroid cancer, nonmedullary
MONDO:0000200	Zimmermann-Laband syndrome
MONDO:0002865	anus sarcoma
MONDO:0002866	duodenal disease
MONDO:0002867	pancreatic cystadenocarcinoma
MONDO:0002860	testis rhabdomyosarcoma
MONDO:0000205	radioulnar synostosis with amegakaryocytic thrombocytopenia
MONDO:0002861	testis sarcoma
MONDO:0000204	skin creases, congenital symmetric circumferential
MONDO:0002862	bile duct sarcoma
MONDO:0000203	Dehydrated hereditary stomatocytosis
MONDO:0002863	rhabdomyosarcoma with mixed embryonal and alveolar features
MONDO:0000202	Heimler syndrome
MONDO:0014828	immunodeficiency-centromeric instability-facial anomalies syndrome 3
MONDO:0014827	autosomal recessive spastic paraplegia type 76
MONDO:0014826	nucleoside diphosphate-linked moiety X Motif 15 deficiency
MONDO:0014825	chromosome 11p13 deletion syndrome, distal
MONDO:0014829	immunodeficiency-centromeric instability-facial anomalies syndrome 4
MONDO:0014831	progeroid and marfanoid aspect-lipodystrophy syndrome
MONDO:0014830	platelet-type bleeding disorder 20
MONDO:0014835	striatal degeneration, autosomal dominant 2
MONDO:0014834	dyskinesia, limb and orofacial, infantile-onset
MONDO:0014833	heart and brain malformation syndrome
MONDO:0014832	intellectual disability, autosomal recessive 53
MONDO:0002857	gallbladder sarcoma
MONDO:0002858	ovary rhabdomyosarcoma
MONDO:0002859	breast rhabdomyosarcoma
MONDO:0002831	non-keratinizing sinonasal squamous cell carcinoma
MONDO:0002832	endometrial transitional cell carcinoma
MONDO:0002833	fallopian tube transitional cell carcinoma
MONDO:0002834	primary prostate urothelial carcinoma
MONDO:0002830	ovary transitional cell carcinoma
MONDO:0014817	nephrotic syndrome, type 12
MONDO:0014816	split-foot malformation-mesoaxial polydactyly syndrome
MONDO:0014815	intellectual disability, autosomal recessive 52
MONDO:0014814	advanced sleep phase syndrome 3
MONDO:0014819	autosomal dominant Robinow syndrome 3
MONDO:0014818	nephrotic syndrome, type 13
MONDO:0014820	mitochondrial DNA depletion syndrome 14 (cardioencephalomyopathic type)
MONDO:0014824	craniofacial dysplasia-short stature-ectodermal anomalies-intellectual disability syndrome
MONDO:0014823	hypotonia, infantile, with psychomotor retardation and characteristic facies 3
MONDO:0014822	15q14 microdeletion syndrome
MONDO:0014821	complex lethal osteochondrodysplasia
MONDO:0002828	Bartholin gland transitional cell carcinoma
MONDO:0002829	bartholin gland carcinoma
MONDO:0002824	extrinsic cardiomyopathy
MONDO:0002825	Meige syndrome
MONDO:0002826	tuberculosis
MONDO:0002827	urinary system cancer
MONDO:0002842	bacterial gastritis
MONDO:0002843	fungal gastritis
MONDO:0002844	lymphocytic gastritis
MONDO:0002845	necrotizing gastritis
MONDO:0002840	eosinophilic gastritis
MONDO:0002841	eosinophilic gastroenteritis
MONDO:0014806	spinal muscular atrophy with congenital bone fractures 1
MONDO:0014805	Hao-Fountain syndrome
MONDO:0014804	sideroblastic anemia 3
MONDO:0014803	spasticity-ataxia-gait anomalies syndrome
MONDO:0014809	DDX41-related hematologic malignancy predisposition syndrome
MONDO:0014808	congenital secretory sodium diarrhea 8
MONDO:0014807	spinal muscular atrophy with congenital bone fractures 2
MONDO:0014813	hypomyelinating leukodystrophy 13
MONDO:0014812	metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration
MONDO:0014811	cerebellar atrophy, visual impairment, and psychomotor retardation;
MONDO:0014810	pancytopenia due to IKZF1 mutations
MONDO:0002839	leather-bottle stomach
MONDO:0002835	papillary transitional carcinoma
MONDO:0002836	urethra transitional cell carcinoma
MONDO:0002837	sarcomatoid transitional cell carcinoma
MONDO:0002838	spindle cell carcinoma
MONDO:0002897	secondary syphilis
MONDO:0000234	Rickettsia parkeri spotted fever
MONDO:0002898	skin cancer
MONDO:0000233	Japanese spotted fever
MONDO:0000232	Flinders island spotted fever
MONDO:0002899	differentiating neuroblastoma
MONDO:0000231	Far eastern spotted fever
MONDO:0000238	pestis minor
MONDO:0002893	chondroid chordoma
MONDO:0002894	spinal chordoma
MONDO:0000237	erysipeloid
MONDO:0002895	dentinogenesis imperfecta
MONDO:0000236	oropharyngeal anthrax
MONDO:0002896	primary syphilis
MONDO:0000235	Rocky mountain spotted fever
MONDO:0002890	gastrointestinal adenoma
MONDO:0012218	dandy-walker malformation with occipital cephalocele, autosomal dominant
MONDO:0002891	gastrointestinal neuroendocrine benign tumor
MONDO:0002892	skull base chordoma
MONDO:0012219	spondyloepiphyseal dysplasia tarda, autosomal recessive, Leroy-Spranger type
MONDO:0000230	Israeli tick typhus
MONDO:0014886	severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome
MONDO:0012223	hypotrichosis, progressive patterned scalp, with wiry hair, onycholysis, and cleft lip/palate
MONDO:0012224	febrile seizures, familial, 6
MONDO:0014885	Hermansky-Pudlak syndrome 10
MONDO:0014884	cholestasis, progressive familial intrahepatic, 5
MONDO:0012221	alpha-N-acetylgalactosaminidase deficiency type 1
MONDO:0012222	alpha-N-acetylgalactosaminidase deficiency type 2
MONDO:0014883	hypertrophic cardiomyopathy 26
MONDO:0012227	myopia 7
MONDO:0014889	striatonigral degeneration, childhood-onset
MONDO:0012228	myopia 8
MONDO:0012225	Senior-Loken syndrome 5
MONDO:0014888	MIRAGE syndrome
MONDO:0014887	bone marrow failure syndrome 3
MONDO:0012226	febrile seizures, familial, 5
MONDO:0000229	Indian tick typhus
MONDO:0000228	Astrakhan spotted fever
MONDO:0014882	hereditary spastic paraplegia 77
MONDO:0012220	Griscelli syndrome type 3
MONDO:0014881	transketolase deficiency
MONDO:0014880	Duane retraction syndrome 3 with or without deafness
MONDO:0000245	tinea imbricata
MONDO:0000244	endothrix infectious disease
MONDO:0000243	ectothrix infectious disease
MONDO:0000242	tinea barbae
MONDO:0000249	secretory diarrhea
MONDO:0000248	dengue shock syndrome
MONDO:0000247	hemophagocytic lymphohistiocytosis
MONDO:0026856	homosexuality 1
MONDO:0000246	la Crosse encephalitis
MONDO:0012209	branchiogenic deafness syndrome
MONDO:0012207	umbilicus, familial flat
MONDO:0012208	congenital reticular ichthyosiform erythroderma
MONDO:0014869	hydrops-lactic acidosis-sideroblastic anemia-multisystemic failure syndrome
MONDO:0000241	Keshan disease
MONDO:0000240	invasive aspergillosis
MONDO:0014875	hyperaldosteronism, familial, type IV
MONDO:0012212	Loeys-Dietz syndrome 1
MONDO:0012213	hereditary spastic paraplegia 26
MONDO:0014874	pontocerebellar hypoplasia, type 2F
MONDO:0014873	nevus comedonicus syndrome
MONDO:0012210	migraine with aura, susceptibility to, 7
MONDO:0014872	congenital stationary night blindness 1H
MONDO:0012211	MPDU1-CDG
MONDO:0014879	patent ductus arteriosus 3
MONDO:0012216	foveal hypoplasia - optic nerve decussation defect - anterior segment dysgenesis syndrome
MONDO:0014878	patent ductus arteriosus 2
MONDO:0012217	Bruck syndrome 2
MONDO:0012214	glucocorticoid deficiency 3
MONDO:0014877	myopathy, distal, 5
MONDO:0012215	myofibrillar myopathy 3
MONDO:0014876	intellectual disability, autosomal recessive 54
MONDO:0000239	adiaspiromycosis
MONDO:0014871	retinitis pigmentosa 75
MONDO:0014870	NEK9-related lethal skeletal dysplasia
MONDO:0000212	hypercalcemia, infantile
MONDO:0002875	parasitic ectoparasitic infectious disease
MONDO:0002876	cervical adenosarcoma
MONDO:0000211	striatal degeneration, autosomal dominant
MONDO:0002877	cervical carcinosarcoma
MONDO:0000210	thiopurine metabolic disease
MONDO:0002878	uterine corpus adenosarcoma
MONDO:0002871	testicular trophoblastic tumor
MONDO:0000216	congenital bilateral aplasia of vas deferens
MONDO:0002872	trophoblastic neoplasm
MONDO:0000215	epilepsy, familial focal, with variable foci
MONDO:0000214	hypermanganesemia with dystonia
MONDO:0002873	testicular germ cell tumor non-seminomatous
MONDO:0000213	autoimmune disease, multisystem, infantile-onset
MONDO:0002874	testicular pure germ cell tumor
MONDO:0014859	developmental and epileptic encephalopathy, 37
MONDO:0002870	tricuspid valve insufficiency
MONDO:0014858	intellectual disability, autosomal dominant 43
MONDO:0014864	hypermanganesemia with dystonia 2
MONDO:0012201	tibia, bowing of, with pseudarthrosis and pectus excavatum
MONDO:0014863	macrocephaly, dysmorphic facies, and psychomotor retardation
MONDO:0012202	malaria, mild, susceptibility to
MONDO:0014862	cerebral palsy, spastic quadriplegic, 3
MONDO:0014861	autoimmune disease, multisystem, infantile-onset, 2
MONDO:0012200	posterior polymorphous corneal dystrophy 3
MONDO:0014868	developmental and epileptic encephalopathy, 38
MONDO:0012205	autosomal dominant striatal neurodegeneration type 1
MONDO:0014867	spinocerebellar ataxia 43
MONDO:0012206	Czech dysplasia, metatarsal type
MONDO:0014866	Charcot-Marie-Tooth disease axonal type 2T
MONDO:0012203	familial hyperthyroidism due to mutations in TSH receptor
MONDO:0012204	familial pseudohyperkalemia
MONDO:0014865	autosomal recessive severe congenital neutropenia due to CSF3R deficiency
MONDO:0000209	prenatal-onset spinal muscular atrophy with congenital bone fractures
MONDO:0000208	microcephaly, short stature, and impaired glucose metabolism 1
MONDO:0000207	hypotonia, infantile, with psychomotor retardation and characteristic facies
MONDO:0000206	cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy
MONDO:0002868	bile duct mucinous cystic neoplasm with an associated invasive carcinoma
MONDO:0014860	polycystic liver disease 2
MONDO:0002869	heart valve disease
MONDO:0002886	common bile duct disease
MONDO:0000223	chikungunya
MONDO:0002887	bile duct disease
MONDO:0000222	seminal vesicle acute gonorrhea
MONDO:0002888	intraorbital meningioma
MONDO:0000221	cerebroretinal microangiopathy with calcifications and cysts
MONDO:0002889	orbital cancer
MONDO:0000220	anterior segment dysgenesis
MONDO:0000227	African tick-bite fever
MONDO:0002882	colon neuroendocrine neoplasm
MONDO:0002883	intestinal neuroendocrine neoplasm
MONDO:0000226	mineral metabolism disease
MONDO:0000225	human monocytic ehrlichiosis
MONDO:0002884	nail disease
MONDO:0000224	acquired carbohydrate metabolism disease
MONDO:0002885	erythrasma
MONDO:0014849	autosomal recessive nonsyndromic deafness 105
MONDO:0002880	ovarian adenosarcoma
MONDO:0014848	TELO2-related intellectual disability-neurodevelopmental disorder
MONDO:0002881	vaginal adenosarcoma
MONDO:0014847	spermatogenic failure 15
MONDO:0014853	autosomal dominant nonsyndromic deafness 70
MONDO:0014852	palmoplantar carcinoma, multiple self-healing
MONDO:0014851	hypercalcemia, infantile 2
MONDO:0014850	retinitis pigmentosa and erythrocytic microcytosis
MONDO:0014857	neurodevelopmental disorder with or without anomalies of the brain, eye, or heart
MONDO:0014856	combined oxidative phosphorylation defect type 30
MONDO:0014855	intellectual disability, autosomal dominant 42
MONDO:0014854	autosomal dominant nonsyndromic deafness 66
MONDO:0000219	uncombable hair syndrome
MONDO:0000218	preimplantation embryonic lethality
MONDO:0000217	Frontometaphyseal dysplasia
MONDO:0002879	uterine body mixed cancer
MONDO:0002810	pancreatic serous cystic neoplasm
MONDO:0002811	main bronchus cancer
MONDO:0002812	infectious otitis interna
MONDO:0014802	Cowden syndrome 7
MONDO:0014801	even-plus syndrome
MONDO:0014800	progressive scapulohumeroperoneal distal myopathy
MONDO:0002806	bronchogenic carcinoma
MONDO:0002807	bronchial neoplasm
MONDO:0002808	pancreatic serous cystadenoma
MONDO:0002809	pancreatic cystadenoma
MONDO:0002802	functional colonic disease
MONDO:0002803	intestinal pseudo-obstruction
MONDO:0002804	apocrine adenoma
MONDO:0002805	hidradenoma
MONDO:0002820	thyroid carcinoma
MONDO:0002821	trabecular follicular adenocarcinoma
MONDO:0002822	trabecular adenocarcinoma
MONDO:0002823	thyroid gland medullary carcinoma
MONDO:0002817	adrenal gland cancer
MONDO:0002818	adrenal cortical adenocarcinoma
MONDO:0002819	Loeffler endocarditis
MONDO:0002813	lipomatous cancer
MONDO:0002814	adrenal carcinoma
MONDO:0002815	acute myocarditis
MONDO:0002816	adrenal cortex disease
MONDO:0002800	thrombophlebitis
MONDO:0002801	colonic pseudo-obstruction
MONDO:0024299	vitamin D-dependent rickets
MONDO:0024292	gastrointestinal polyp
MONDO:0024291	vascular malformation
MONDO:0024294	skin disease caused by infection
MONDO:0024293	polyposis, gastric, Dos Santos and de Magalhaes 1980
MONDO:0024296	vascular neoplasm
MONDO:0024295	skin disease caused by bacterial infection
MONDO:0024298	vitamin deficiency disorder
MONDO:0024297	nutritional or metabolic disease
MONDO:0024290	enuresis
MONDO:0024245	ductal eccrine adenocarcinoma
MONDO:0000278	Bolivian hemorrhagic fever
MONDO:0000277	Argentine hemorrhagic fever
MONDO:0024247	benign eccrine neoplasm
MONDO:0000276	Powassan encephalitis
MONDO:0024246	syringofibroadenoma
MONDO:0000275	monogenic disease
MONDO:0024249	pityriasis lichenoides
MONDO:0024248	pityriasis
MONDO:0000279	Venezuelan hemorrhagic fever
MONDO:0000270	lower respiratory tract disease
MONDO:0000274	tick-borne encephalitis
MONDO:0024240	eccrine carcinoma
MONDO:0000273	Kunjin virus infectous disease
MONDO:0000272	autoimmune polyendocrine syndrome type 2
MONDO:0000271	tuberculous salpingitis
MONDO:0012267	holoprosencephaly 8
MONDO:0012268	AIDS
MONDO:0012265	preeclampsia/eclampsia 3
MONDO:0012266	preeclampsia/eclampsia 4
MONDO:0012269	chromosome 3q29 microdeletion syndrome
MONDO:0012260	cataract 35
MONDO:0012263	autoimmune disease, susceptibility to, 4
MONDO:0012264	preeclampsia/eclampsia 2
MONDO:0012261	autism, susceptibility to, 6
MONDO:0012262	fibrosis of extraocular muscles, congenital, 3c
MONDO:0024234	Seckel like syndrome majoor-krakauer type
MONDO:0000289	selective IgM deficiency disease
MONDO:0000288	polycystic echinococcosis
MONDO:0000287	Lambert-Eaton myasthenic syndrome
MONDO:0024236	degenerative disorder
MONDO:0000286	Epstein-Barr virus hepatitis
MONDO:0024235	Brenner tumor
MONDO:0024238	cerebral degeneration
MONDO:0024237	inherited neurodegenerative disorder
MONDO:0024239	congenital anomaly of cardiovascular system
MONDO:0000281	Chapare hemorrhagic fever
MONDO:0000280	Brazilian hemorrhagic fever
MONDO:0000285	lujo hemorrhagic fever
MONDO:0000284	Hantavirus hemorrhagic fever with renal syndrome, Puumala virus type
MONDO:0000283	Hantavirus hemorrhagic fever with renal syndrome, Seoul virus type
MONDO:0000282	Whitewater Arroyo hemorrhagic fever
MONDO:0012256	hereditary spastic paraplegia 28
MONDO:0012257	Cerebrorenodigital syndrome
MONDO:0012254	multiple epiphyseal dysplasia, with miniepiphyses
MONDO:0012255	chromosome 18 pericentric inversion
MONDO:0012258	epidermolysis bullosa simplex with circinate migratory erythema
MONDO:0012259	colloid cysts of third ventricle
MONDO:0012252	rhabdoid tumor predisposition syndrome 1
MONDO:0012253	multiple epiphyseal dysplasia, with severe proximal femoral dysplasia
MONDO:0012250	Charcot-Marie-Tooth disease type 4H
MONDO:0012251	MEDNIK syndrome
MONDO:0000256	systemic mycosis
MONDO:0000255	subcutaneous mycosis
MONDO:0000254	cutaneous mycosis
MONDO:0000253	piedra
MONDO:0024227	miliaria pustulosa
MONDO:0000259	asymptomatic dengue
MONDO:0024229	miliaria crystallina
MONDO:0000258	intestinal botulism
MONDO:0024228	miliaria profunda
MONDO:0000257	acute diarrhea
MONDO:0000252	inflammatory diarrhea
MONDO:0000251	diarrheal disease secondary to altered bowel motility
MONDO:0000250	osmotic diarrheal disease
MONDO:0012245	developmental and epileptic encephalopathy, 3
MONDO:0012246	spinocerebellar ataxia type 26
MONDO:0012243	B-cell immunodeficiency, distal limb anomalies, and urogenital malformations
MONDO:0012244	prostate cancer, hereditary, 5
MONDO:0012249	colorectal cancer, hereditary nonpolyposis, type 2
MONDO:0012247	spinocerebellar ataxia type 27
MONDO:0012248	autosomal recessive limb-girdle muscular dystrophy type 2K
MONDO:0012241	progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 3
MONDO:0012242	syncope, familial vasovagal
MONDO:0012240	nemaline myopathy 4
MONDO:0000267	cryptogenic organizing pneumonia
MONDO:0000266	pulmonary aspergilloma
MONDO:0000265	aspiration pneumonia
MONDO:0000264	Pontiac fever
MONDO:0000269	inhalation anthrax
MONDO:0000268	lymphoid interstitial pneumonia
MONDO:0012229	myopia 9
MONDO:0000263	laryngotracheitis
MONDO:0000262	otomycosis
MONDO:0000261	adenoiditis
MONDO:0000260	Kartagener syndrome
MONDO:0014897	portal hypertension, noncirrhotic
MONDO:0012234	LFS3
MONDO:0012235	autosomal recessive spinocerebellar ataxia 7
MONDO:0014896	congenital muscular dystrophy-respiratory failure-skin abnormalities-joint hyperlaxity syndrome
MONDO:0012232	stuttering, familial persistent, 2
MONDO:0014895	developmental and epileptic encephalopathy, 40
MONDO:0012233	Li-Fraumeni syndrome 2
MONDO:0014894	Meier-Gorlin syndrome 7
MONDO:0012238	progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 2
MONDO:0012239	nemaline myopathy 1
MONDO:0014899	adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency
MONDO:0012236	keratoconus 4
MONDO:0012237	nemaline myopathy 6
MONDO:0014898	progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 3
MONDO:0012230	myopia 10
MONDO:0014893	Okur-Chung neurodevelopmental syndrome
MONDO:0012231	Charcot-Marie-Tooth disease type 2A2
MONDO:0014892	micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome
MONDO:0014891	hyperuricemic nephropathy, familial juvenile type 4
MONDO:0014890	PERCHING syndrome
MONDO:0024289	disorder of bilirubin metabolism
MONDO:0024288	hyperbilirubinemia
MONDO:0024281	juvenile chronic polyarthritis
MONDO:0024280	polyarticular arthritis
MONDO:0024283	Demodex folliculitis
MONDO:0024282	mucinous ovarian cancer
MONDO:0024285	epsilon-heavy chain disease
MONDO:0024284	demodicidosis of sebaceous gland
MONDO:0024287	congenital vascular malformation
MONDO:0024286	benign blood vessel neoplasm
MONDO:0024278	proctocolitis
MONDO:0024277	neonatal thrombocytopenia
MONDO:0024279	chronic endometritis
MONDO:0024270	parasitic intestinal disease
MONDO:0024271	intestinal helminthiasis
MONDO:0024276	glandular cell neoplasm
MONDO:0024275	amebic dysentery
MONDO:0012298	omphalocele, diaphragmatic hernia, and radial ray defects
MONDO:0012299	nanophthalmos 2
MONDO:0012292	hepatitis C virus, susceptibility to
MONDO:0012293	autosomal recessive nonsyndromic deafness 23
MONDO:0012290	CEDNIK syndrome
MONDO:0012291	immunoglobulin A deficiency 2
MONDO:0012296	lipomyelomeningocele
MONDO:0012297	SPOAN syndrome
MONDO:0012294	drug metabolism, poor, Cyp2C19-related
MONDO:0012295	complement component 5 deficiency
MONDO:0024267	epidemic encephalitis
MONDO:0024266	patent ductus arteriosus 3
MONDO:0000299	thelaziasis
MONDO:0000298	dioctophymiasis
MONDO:0000297	baylisascariasis
MONDO:0024268	superficial mycosis
MONDO:0000292	philophthalmiasis
MONDO:0000291	granulomatous amebic encephalitis
MONDO:0000290	primary amebic meningoencephalitis
MONDO:0000296	angiostrongyliasis
MONDO:0024263	neonatal aspiration syndrome
MONDO:0000295	acanthocephaliasis
MONDO:0024262	massive neonatal aspiration syndrome
MONDO:0000294	mesocestoidiasis
MONDO:0024265	Duane syndrome type 1
MONDO:0024264	hypothyroidism, congenital, nongoitrous, 2
MONDO:0000293	coenurosis
MONDO:0012289	myofibrillar myopathy 5
MONDO:0012287	Stickler syndrome, type I, nonsyndromic ocular
MONDO:0012288	iridogoniodysgenesis and skeletal anomalies
MONDO:0012281	sarcoidosis, early-onset
MONDO:0012282	Al-Gazali syndrome
MONDO:0012280	Goldberg-Shprintzen megacolon syndrome
MONDO:0012285	left ventricular noncompaction 2
MONDO:0012286	myopathy, autophagic vacuolar, infantile-onset
MONDO:0012283	cleft palate, midfacial hypoplasia, triangular facies, and sensorineural hearing loss
MONDO:0012284	nephropathy, progressive, with deafness
MONDO:0024255	genetic skin disease
MONDO:0024257	hereditary motor neuron disease
MONDO:0024250	acute lichenoid pityriasis
MONDO:0024252	global developmental delay-neuro-ophthalmological abnormalities-seizures-intellectual disability syndrome
MONDO:0024251	Minamata disease
MONDO:0024254	vibratory angioedema
MONDO:0012278	supranuclear palsy, progressive, 2
MONDO:0012279	congenital muscular dystrophy merosin-positive
MONDO:0012276	generalized epilepsy-paroxysmal dyskinesia syndrome
MONDO:0012277	myofibrillar myopathy 4
MONDO:0012270	Tukel syndrome
MONDO:0012271	mesoaxial synostotic syndactyly with phalangeal reduction
MONDO:0012274	acromesomelic dysplasia, Demirhan type
MONDO:0012275	fetal valproate syndrome
MONDO:0012272	intellectual disability, keratoconus, febrile seizures, and sinoatrial block
MONDO:0012273	autosomal recessive nonsyndromic deafness 48
MONDO:0002732	lung benign neoplasm
MONDO:0002734	anal mucinous adenocarcinoma
MONDO:0002735	anal canal adenocarcinoma
MONDO:0002730	childhood kidney neoplasm
MONDO:0002731	cerebral hemisphere cancer
MONDO:0014718	developmental and epileptic encephalopathy, 34
MONDO:0014717	early-onset Lafora body disease
MONDO:0014716	macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome
MONDO:0014715	primary immunodeficiency with post-measles-mumps-rubella vaccine viral infection
MONDO:0014719	developmental and epileptic encephalopathy, 35
MONDO:0014721	hereditary spherocytosis type 2
MONDO:0014720	autosomal dominant optic atrophy plus syndrome
MONDO:0014725	spastic tetraplegia-thin corpus callosum-progressive postnatal microcephaly syndrome
MONDO:0014724	Joubert syndrome 24
MONDO:0014723	PMP22-RAI1 contiguous gene duplication syndrome
MONDO:0014722	Roifman syndrome
MONDO:0002729	rhabdoid tumor of the kidney
MONDO:0002725	diffuse cutaneous mastocytosis
MONDO:0002726	cutaneous solitary mastocytoma
MONDO:0002727	olfactory nerve disease
MONDO:0002728	rhabdoid tumor
MONDO:0002743	prostate colloid adenocarcinoma
MONDO:0002744	fallopian tube mucinous adenocarcinoma
MONDO:0002745	fallopian tube mucinous tumor
MONDO:0002746	fallopian tube adenocarcinoma
MONDO:0002740	uterine ligament mucinous adenocarcinoma
MONDO:0002741	uterine ligament adenocarcinoma
MONDO:0002742	cervical mucinous adenocarcinoma
MONDO:0014707	14q32 duplication syndrome
MONDO:0014706	cutis laxa, autosomal dominant 3
MONDO:0014705	craniosynostosis 6
MONDO:0014704	skeletal overgrowth-craniofacial dysmorphism-hyperelastic skin-white matter lesions syndrome
MONDO:0014709	Heimler syndrome 2
MONDO:0014708	ring chromosome 14
MONDO:0014710	autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency
MONDO:0014714	progressive microcephaly-seizures-cortical blindness-developmental delay syndrome
MONDO:0014713	porokeratosis 9, multiple types
MONDO:0014712	Senior-Loken syndrome 9
MONDO:0014711	autosomal dominant Charcot-Marie-Tooth disease type 2W
MONDO:0002736	ampulla of vater mucinous adenocarcinoma
MONDO:0002737	acute sanguinous otitis media
MONDO:0002738	acute transudative otitis media
MONDO:0002739	extrahepatic bile duct mucinous adenocarcinoma
MONDO:0002710	infiltrating angiolipoma
MONDO:0002711	angiolipoma
MONDO:0002712	epidural spinal canal angiolipoma
MONDO:0002713	epidural spinal canal neoplasm
MONDO:0014703	Adams-Oliver syndrome 6
MONDO:0014702	autosomal recessive complex spastic paraplegia type 9B
MONDO:0014701	spondyloepiphyseal dysplasia, Stanescu type
MONDO:0014700	neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-hip dysplasia syndrome due to a point mutation
MONDO:0002707	breast mucinous carcinoma
MONDO:0002708	retinitis
MONDO:0002709	Kallmann syndrome
MONDO:0002703	appendix mucinous cystadenocarcinoma
MONDO:0002704	appendix adenocarcinoma
MONDO:0002705	breast mucinous cystadenocarcinoma
MONDO:0002706	cervix endometriosis
MONDO:0002721	necrosis of pituitary
MONDO:0002722	olfactory nerve neoplasm
MONDO:0002723	cutaneous mastocytosis
MONDO:0002724	mast cell neoplasm
MONDO:0002720	sella turcica neoplasm
MONDO:0002718	central nervous system teratoma
MONDO:0002719	conus medullaris neoplasm
MONDO:0002714	central nervous system cancer
MONDO:0002715	uterine cancer
MONDO:0002716	childhood spinal cord tumor
MONDO:0002717	spinal cord intramedullary teratoma
MONDO:0002776	external ear disease
MONDO:0000113	cerebellar ataxia, mental retardation, and dysequilibrium syndrome
MONDO:0000112	cardioencephalomyopathy, fatal infantile
MONDO:0002777	pleural empyema
MONDO:0002778	epidural spinal canal meningioma
MONDO:0000111	camptodactyly syndrome, Guadalajara
MONDO:0002779	central nervous system chondroma
MONDO:0000110	bifid nose
MONDO:0002772	intraventricular meningioma
MONDO:0000117	diarrhea, congenital
MONDO:0000116	cortical dysplasia, complex, with other brain malformations
MONDO:0000115	Chiari malformation
MONDO:0002774	chordoid glioma
MONDO:0002775	anovulation
MONDO:0000114	cerebelloparenchymal disorder
MONDO:0002770	vaginal discharge
MONDO:0002771	pulmonary fibrosis
MONDO:0014759	intellectual disability, autosomal recessive 51
MONDO:0014765	woolly hair, autosomal recessive 3
MONDO:0012102	glaucoma 1, open angle, K
MONDO:0012103	spinocerebellar ataxia type 25
MONDO:0014764	spastic paraplegia-severe developmental delay-epilepsy syndrome
MONDO:0012100	major depressive disorder 2
MONDO:0014763	Bombay phenotype
MONDO:0012101	glaucoma 1, open angle, J
MONDO:0014762	heterotaxy, visceral, 7, autosomal
MONDO:0012106	microcephaly 5, primary, autosomal recessive
MONDO:0014769	inherited oocyte maturation defect
MONDO:0012107	neuropathy, hereditary sensory and autonomic, adult-onset, with anosmia
MONDO:0014768	cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2
MONDO:0012104	acquired partial lipodystrophy
MONDO:0014767	Seckel syndrome 9
MONDO:0012105	granulomatosis with polyangiitis
MONDO:0014766	leukodystrophy and acquired microcephaly with or without dystonia;
MONDO:0000109	basal ganglia calcification, idiopathic
MONDO:0000108	bacteremia, susceptibility
MONDO:0000107	auriculocondylar syndrome
MONDO:0002769	leukorrhea
MONDO:0014761	hereditary pediatric Behçet-like disease
MONDO:0014760	TFRC-related combined immunodeficiency
MONDO:0026732	hypothyroidism, congenital, nongoitrous, 9
MONDO:0002787	adamantinous craniopharyngioma
MONDO:0000124	focal facial dermal dysplasia
MONDO:0002788	papillary craniopharyngioma
MONDO:0026733	intellectual developmental disorder, X-linked, syndromic, Hackmann-Di Donato type
MONDO:0000123	factor V and Factor VIII, combined deficiency of
MONDO:0002789	hemangiopericytic tumor
MONDO:0026730	Basilicata-Akhtar syndrome
MONDO:0000122	facial paresis, hereditary congenital
MONDO:0026731	hypothyroidism, congenital, nongoitrous, 8
MONDO:0000121	emphysema
MONDO:0002783	Shwartzman phenomenon
MONDO:0000128	giant axonal neuropathy
MONDO:0000127	geleophysic dysplasia
MONDO:0002784	craniopharyngioma
MONDO:0002785	skull base neoplasm
MONDO:0000126	gastric cancer
MONDO:0002786	diencephalic cancer
MONDO:0000125	fundus dystrophy, pseudoinflammatory
MONDO:0014749	tooth agenesis, selective, 7
MONDO:0002781	glossopharyngeal nerve paralysis
MONDO:0002782	cranial nerve palsy
MONDO:0014748	progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome
MONDO:0000120	ectopia lentis, isolated
MONDO:0014754	primary coenzyme Q10 deficiency 8
MONDO:0014753	autosomal recessive optic atrophy
MONDO:0014752	nephrotic syndrome, type 11
MONDO:0014751	palatal anomalies-widely spaced teeth-facial dysmorphism-developmental delay syndrome
MONDO:0014758	radioulnar synostosis with amegakaryocytic thrombocytopenia 2
MONDO:0014757	macrothrombocytopenia-lymphedema-developmental delay-facial dysmorphism-camptodactyly syndrome
MONDO:0014756	tremor, hereditary essential, 5
MONDO:0014755	skin creases, congenital symmetric circumferential, 2
MONDO:0026729	congenital disorder of glycosylation, type ICC
MONDO:0026727	Shukla-Vernon syndrome
MONDO:0000119	congenital heart defects, multiple types
MONDO:0000118	reticulate pigment disorder
MONDO:0014750	primary ciliary dyskinesia 33
MONDO:0002754	extramedullary plasmacytoma
MONDO:0026721	mitochondrial complex 1 deficiency, nuclear type 30
MONDO:0026722	Mullegama-Klein-Martinez syndrome
MONDO:0002755	solitary osseous plasmacytoma
MONDO:0002756	solitary plasmacytoma of chest wall
MONDO:0026720	mitochondrial complex 1 deficiency, nuclear type 12
MONDO:0002757	acute allergic sanguinous otitis media
MONDO:0002750	bladder colloid adenocarcinoma
MONDO:0026726	nephrotic syndrome, type 20
MONDO:0002751	bladder adenocarcinoma
MONDO:0002752	ovarian adenocarcinoma
MONDO:0026723	intellectual developmental disorder, X-linked 108
MONDO:0002753	mucinous stomach adenocarcinoma
MONDO:0026724	Paganini-Miozzo syndrome
MONDO:0014739	autosomal recessive nonsyndromic deafness 97
MONDO:0014738	autosomal dominant nonsyndromic deafness 69
MONDO:0014737	dehydrated hereditary stomatocytosis 2
MONDO:0014743	rhizomelic chondrodysplasia punctata type 5
MONDO:0014742	Parkinson disease 22, autosomal dominant
MONDO:0014741	facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation
MONDO:0014740	autosomal dominant nonsyndromic deafness 68
MONDO:0014747	familial progressive retinal dystrophy-iris coloboma-congenital cataract syndrome
MONDO:0014746	SLC39A8-CDG
MONDO:0014745	congenital myasthenic syndrome 19
MONDO:0014744	acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome
MONDO:0002747	endometrial mucinous adenocarcinoma
MONDO:0002748	rectum mucinous adenocarcinoma
MONDO:0002749	extracranial neuroblastoma
MONDO:0002765	plantar verrucous skin carcinoma
MONDO:0000102	vertigo
MONDO:0002766	larynx verrucous carcinoma
MONDO:0000101	tumoral calcinosis
MONDO:0000100	trichorhinophalangeal syndrome
MONDO:0002767	protein C deficiency
MONDO:0002768	true hermaphroditism
MONDO:0002761	cervical verrucous carcinoma
MONDO:0000106	apnea
MONDO:0002762	esophagus verrucous carcinoma
MONDO:0000105	anemia, nonspherocytic hemolytic
MONDO:0002763	urethral verrucous carcinoma
MONDO:0000104	anemia, hypochromic microcytic with iron overload
MONDO:0002764	urethra squamous cell carcinoma
MONDO:0000103	Wilms tumor
MONDO:0014729	hereditary spastic paraplegia 75
MONDO:0014728	combined oxidative phosphorylation defect type 27
MONDO:0014727	immunodeficiency 45
MONDO:0014726	Charcot-Marie-Tooth disease axonal type 2X
MONDO:0002760	bladder squamous cell carcinoma
MONDO:0014732	hypomyelinating leukodystrophy 12
MONDO:0014731	seizures-scoliosis-macrocephaly syndrome
MONDO:0014730	microcephaly 16, primary, autosomal recessive
MONDO:0014736	Charcot-Marie-Tooth disease axonal type 2Z
MONDO:0014735	Charcot-Marie-Tooth disease type 2Y
MONDO:0014734	epilepsy, idiopathic generalized, susceptibility to, 14
MONDO:0014733	Charcot-Marie-Tooth disease type 4K
MONDO:0002758	vulva verrucous carcinoma
MONDO:0002759	bladder verrucous carcinoma
MONDO:0002700	epithelioid trophoblastic tumor
MONDO:0002701	ovarian mucinous cystadenocarcinoma
MONDO:0002702	ovarian cystadenocarcinoma
MONDO:0024182	dry beriberi
MONDO:0024183	wet beriberi
MONDO:0012190	nephrotic syndrome - deafness - pretibial epidermolysis bullosa syndrome
MONDO:0024171	radio-digito-facial dysplasia
MONDO:0012199	posterior polymorphous corneal dystrophy 2
MONDO:0012193	autosomal dominant limb-girdle muscular dystrophy type 1G
MONDO:0012194	aneurysm, intracranial berry, 3
MONDO:0012191	hepatoencephalopathy due to combined oxidative phosphorylation defect type 1
MONDO:0012192	permanent neonatal diabetes mellitus-pancreatic and cerebellar agenesis syndrome
MONDO:0012197	idiopathic aplastic anemia
MONDO:0012198	PCWH syndrome
MONDO:0012195	arthrogryposis-severe scoliosis syndrome
MONDO:0012196	autosomal dominant auditory neuropathy 1
MONDO:0000157	episodic pain syndrome, familial
MONDO:0000156	trigonocephaly
MONDO:0000155	triglyceride storage disease
MONDO:0000154	Trichohepatoenteric syndrome
MONDO:0000159	bone marrow failure syndrome
MONDO:0000158	developmental dysplasia of the hip
MONDO:0000153	transposition of the great arteries
MONDO:0000152	thiamine-responsive dysfunction syndrome
MONDO:0000151	symphalangism
MONDO:0000150	spondylometaphyseal dysplasia
MONDO:0026782	chondrodysplasia punctata 2, X-linked dominant
MONDO:0012146	familial hemophagocytic lymphohistiocytosis 3
MONDO:0012147	coronary heart disease, susceptibility to, 5
MONDO:0012144	Waardenburg syndrome type 2D
MONDO:0012145	macular degeneration, age-related, 3
MONDO:0012148	drug metabolism, poor, CYP2D6-related
MONDO:0012149	attention deficit-hyperactivity disorder, susceptibility to, 1
MONDO:0012142	orofacial cleft 5
MONDO:0012143	hereditary cryohydrocytosis with reduced stomatin
MONDO:0012140	pulmonary function
MONDO:0012141	orofacial cleft 6, susceptibility to
MONDO:0000168	mental retardation, X-linked, nonsyndromic
MONDO:0000167	Huntington disease and related disorders
MONDO:0026777	VEXAS syndrome
MONDO:0000166	encephalopathy, acute, infection-induced
MONDO:0000165	ectodermal dysplasia-syndactyly syndrome
MONDO:0000169	microphthalmia, isolated, with cataract
MONDO:0000160	epilepsy, familial adult myoclonic
MONDO:0000164	corneal dystrophy, Fuchs endothelial
MONDO:0000163	breast-ovarian cancer, familial, susceptibility to
MONDO:0000162	autoimmune thyroid disease, susceptibility to
MONDO:0000161	adrenal hyperplasia
MONDO:0026771	developmental and epileptic encephalopathy, 85, with or without midline brain defects
MONDO:0012135	restless legs syndrome, susceptibility to, 2
MONDO:0014798	brachydactyly type A1D
MONDO:0012136	carnitine palmitoyl transferase II deficiency, neonatal form
MONDO:0014797	lymphatic malformation 6
MONDO:0014796	autosomal recessive early-onset Parkinson disease 23
MONDO:0012133	lateral semicircular canal malformation, familial, with external and middle ear abnormalities
MONDO:0012134	myoclonic epilepsy, juvenile, susceptibility to, 3
MONDO:0014795	exercise intolerance, riboflavin-responsive
MONDO:0012139	macular dystrophy, retinal, 3
MONDO:0012137	Carney complex - trismus - pseudocamptodactyly syndrome
MONDO:0014799	cataract 45
MONDO:0012138	muscular dystrophy-dystroglycanopathy type B6
MONDO:0014790	TMEM199-CDG
MONDO:0012131	metaphyseal undermodeling, spondylar dysplasia, and overgrowth
MONDO:0014794	Meier-Gorlin syndrome 6
MONDO:0012132	colorectal cancer, susceptibility to, 1
MONDO:0014793	microcephaly-congenital cataract-psoriasiform dermatitis syndrome
MONDO:0014792	Paget disease of bone 6
MONDO:0012130	myofibrillar myopathy 2
MONDO:0014791	Luscan-Lumish syndrome
MONDO:0002798	childhood central nervous system primitive neuroectodermal neoplasm
MONDO:0000135	Kenny-Caffey syndrome
MONDO:0026765	congenital disorder of glycosylation, type IIr
MONDO:0002799	nodular medulloblastoma
MONDO:0000134	inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia
MONDO:0000133	immunodeficiency-centromeric instability-facial anomalies syndrome
MONDO:0026763	holoprosencephaly 13, X-linked
MONDO:0000132	hypocalcemia
MONDO:0002794	adult medulloblastoma
MONDO:0000139	microcephalic primordial dwarfism
MONDO:0002795	adult central nervous system primitive neuroectodermal neoplasm
MONDO:0000138	metaphyseal chondrodysplasia
MONDO:0002796	melanotic medulloblastoma
MONDO:0026767	immunodeficiency 74, COVID-19-related, X-linked
MONDO:0000137	leukoencephalopathy, megalencephalic
MONDO:0026768	warfarin sensitivity, X-linked
MONDO:0002797	childhood medulloblastoma
MONDO:0000136	keratosis follicularis spinulosa decalvans
MONDO:0002790	seminal vesicle tumor
MONDO:0002791	large cell medulloblastoma
MONDO:0012119	asperger syndrome, susceptibility to, 3
MONDO:0002792	cerebellar vermis medulloblastoma
MONDO:0002793	medullomyoblastoma
MONDO:0000131	hyperpigmentation, familial progressive
MONDO:0000130	hypercarotenemia and vitamin a deficiency
MONDO:0026762	Wieacker-Wolff syndrome, female-restricted
MONDO:0012124	sudden infant death-dysgenesis of the testes syndrome
MONDO:0014787	severe intellectual disability-corpus callosum agenesis-facial dysmorphism-cerebellar ataxia syndrome
MONDO:0012125	hypomyelinating leukodystrophy 2
MONDO:0014786	IgA nephropathy, susceptibility to, 3
MONDO:0014785	microcephaly, short stature, and impaired glucose metabolism 2
MONDO:0012122	moyamoya disease 3
MONDO:0012123	congenital disorder of glycosylation type 1E
MONDO:0014784	severe hypotonia-psychomotor developmental delay-strabismus-cardiac septal defect syndrome
MONDO:0012128	dextro-looped transposition of the great arteries 1
MONDO:0012129	leukoencephalopathy, arthritis, colitis, and hypogammaglobulinema
MONDO:0012126	familial avascular necrosis of femoral head
MONDO:0014789	CCDC115-CDG
MONDO:0014788	autosomal recessive limb-girdle muscular dystrophy type 2W
MONDO:0012127	autosomal recessive limb-girdle muscular dystrophy type 2J
MONDO:0000129	glutaric aciduria
MONDO:0012120	pyruvate dehydrogenase phosphatase deficiency
MONDO:0014783	preimplantation embryonic lethality 1
MONDO:0014782	autosomal recessive limb-girdle muscular dystrophy type 2X
MONDO:0012121	otosclerosis 5
MONDO:0014781	combined oxidative phosphorylation deficiency 29
MONDO:0014780	hyperphosphatasia with intellectual disability syndrome 6
MONDO:0000146	progeroid syndrome
MONDO:0026754	histidinuria-renal tubular defect syndrome
MONDO:0000145	premature aging syndrome
MONDO:0000144	pregnancy loss, recurrent, susceptibility
MONDO:0000143	multiple mitochondrial dysfunctions syndrome
MONDO:0000149	retinopathy
MONDO:0000148	pulmonary fibrosis and/or bone marrow failure, telomere-related
MONDO:0000147	polyposis
MONDO:0012108	spondyloepimetaphyseal dysplasia, matrilin-3 type
MONDO:0012109	hypertension, essential, susceptibility to, 4
MONDO:0000142	multiple congenital anomalies-hypotonia-seizures syndrome
MONDO:0000141	mosaic variegated aneuploidy syndrome
MONDO:0012113	epilepsy, idiopathic generalized, susceptibility to, 3
MONDO:0014776	spinocerebellar ataxia type 42
MONDO:0012114	Ehlers-Danlos syndrome, Beasley-Cohen type
MONDO:0014775	combined oxidative phosphorylation deficiency 28
MONDO:0012111	hypertrophic cardiomyopathy 8
MONDO:0014774	neuroblastoma, susceptibility to, 7
MONDO:0014773	cardiac anomalies - developmental delay - facial dysmorphism syndrome
MONDO:0012112	hypertrophic cardiomyopathy 10
MONDO:0012117	ALG9-CDG
MONDO:0012118	COG7-CDG
MONDO:0014779	Wilms tumor 6
MONDO:0014778	Lamb-Shaffer syndrome
MONDO:0012115	scoliosis, isolated, susceptibility to, 3
MONDO:0012116	spinocerebellar ataxia type 8
MONDO:0014777	hypotonia, infantile, with psychomotor retardation and characteristic facies 2
MONDO:0014772	orofacial cleft 15
MONDO:0014771	Joubert syndrome 26
MONDO:0012110	growth delay due to insulin-like growth factor type 1 deficiency
MONDO:0014770	Joubert syndrome 25
MONDO:0000199	familial adenomatous polyposis
MONDO:0000198	linear skin defects with multiple congenital anomalies
MONDO:0000193	cortisone reductase deficiency
MONDO:0000192	polyglucosan body myopathy
MONDO:0000191	renal hypodysplasia/aplasia
MONDO:0000190	ventricular fibrillation
MONDO:0000197	singleton-Merten syndrome
MONDO:0000196	ataxia-oculomotor apraxia
MONDO:0000195	atrial standstill
MONDO:0000194	Otofaciocervical syndrome
MONDO:0012188	neuronal ceroid lipofuscinosis 9
MONDO:0012189	Amish infantile epilepsy syndrome
MONDO:0012182	skeletal dysplasia, rhizomelic, with retinitis pigmentosa
MONDO:0012183	melanoma, cutaneous malignant, susceptibility to, 3
MONDO:0012180	arrhythmogenic right ventricular dysplasia 9
MONDO:0012181	hereditary spastic paraplegia 27
MONDO:0012186	Fanconi anemia complementation group I
MONDO:0012187	Fanconi anemia complementation group J
MONDO:0012184	Pierson syndrome
MONDO:0012185	spondylometaphyseal dysplasia, A4 type
MONDO:0012179	narcolepsy 3
MONDO:0012177	posterior column ataxia-retinitis pigmentosa syndrome
MONDO:0012178	intellectual disability with optic atrophy, facial dysmorphism, microcephaly, and short stature
MONDO:0012171	marfanoid habitus with situs inversus
MONDO:0012172	mitochondrial trifunctional protein deficiency
MONDO:0012170	autosomal recessive nonsyndromic deafness 36
MONDO:0012175	cataract 28
MONDO:0012176	Emanuel syndrome
MONDO:0012173	long chain 3-hydroxyacyl-CoA dehydrogenase deficiency
MONDO:0012174	peripheral cone dystrophy
MONDO:0000179	Neu-Laxova syndrome
MONDO:0000178	breasts and/or nipples, aplasia or hypoplasia of
MONDO:0000177	laryngeal abductor paralysis
MONDO:0000176	megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome
MONDO:0000171	muscular dystrophy-dystroglycanopathy, type A
MONDO:0000170	microphthalmia, isolated, with coloboma
MONDO:0000175	ataxia-telangiectasia-like disorder
MONDO:0000174	split-hand/foot malformation with long bone deficiency
MONDO:0000173	muscular dystrophy-dystroglycanopathy, type C
MONDO:0000172	muscular dystrophy-dystroglycanopathy, type B
MONDO:0012168	dyslexia, susceptibility to, 8
MONDO:0012169	premature ovarian failure 3
MONDO:0012166	autosomal dominant sensory ataxia 1
MONDO:0012167	atrial fibrillation, familial, 2
MONDO:0012160	spondylometaphyseal dysplasia-cone-rod dystrophy syndrome
MONDO:0012161	susceptibility to respiratory infections associated with CD8alpha chain mutation
MONDO:0012164	Meacham syndrome
MONDO:0012165	BNAR syndrome
MONDO:0012162	patterned macular dystrophy 2
MONDO:0012163	severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, NK cell-positive
MONDO:0000189	Schindler disease
MONDO:0000188	GLUT1 deficiency syndrome
MONDO:0000187	ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome
MONDO:0000182	congenital myasthenic syndrome with tubular aggregates
MONDO:0000181	microcephaly and chorioretinopathy
MONDO:0000180	inflammatory skin and bowel disease, neonatal
MONDO:0000186	spondyloepimetaphyseal dysplasia with joint laxity
MONDO:0000185	polyposis syndrome, hereditary mixed
MONDO:0000184	congenital vitamin K-dependent coagulation factors combined deficiency
MONDO:0000183	hypertrophic osteoarthropathy, primary
MONDO:0012157	congenital myasthenic syndrome 4C
MONDO:0012158	keratoconus 2
MONDO:0012155	choanal atresia
MONDO:0012156	myasthenic syndrome, congenital, 1B, fast-channel
MONDO:0012159	lung cancer susceptibility 1
MONDO:0012150	attention deficit-hyperactivity disorder, susceptibility to, 2
MONDO:0012153	Alzheimer disease 9
MONDO:0012154	myopia 6
MONDO:0012151	attention deficit-hyperactivity disorder, susceptibility to, 3
MONDO:0012152	attention deficit-hyperactivity disorder, susceptibility to, 4
MONDO:0002611	benign epilepsy with centrotemporal spikes
MONDO:0002612	frontal lobe epilepsy
MONDO:0002613	histrionic personality disorder
MONDO:0002614	bone inflammation disease
MONDO:0002610	purpura
MONDO:0014600	dyskeratosis congenita, autosomal recessive 6
MONDO:0014604	Parkinson disease 21
MONDO:0014603	autosomal dominant nonsyndromic deafness 40
MONDO:0014602	intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome
MONDO:0014601	autosomal recessive spinocerebellar ataxia 20
MONDO:0002608	gangliosidosis GM2
MONDO:0002609	gangliosidosis GM1
MONDO:0002604	pericytic neoplasm
MONDO:0002605	hepatic angiomyolipoma
MONDO:0002606	epithelioid type angiomyolipoma
MONDO:0002607	lymphangioleiomyomatosis
MONDO:0002622	multifocal osteogenic sarcoma
MONDO:0002623	pediatric osteosarcoma
MONDO:0002624	bone leiomyosarcoma
MONDO:0002625	Ewing sarcoma of bone
MONDO:0002620	localized osteosarcoma
MONDO:0002621	extraosseous osteosarcoma
MONDO:0002619	bone fibrosarcoma
MONDO:0002615	xanthomatosis
MONDO:0002616	mesenchymal cell neoplasm
MONDO:0002617	bone angiosarcoma
MONDO:0002618	undifferentiated high grade pleomorphic sarcoma of bone
MONDO:0002600	mixed germ cell cancer
MONDO:0002601	teratoma
MONDO:0002602	central nervous system disease
MONDO:0002603	angiomyolipoma
MONDO:0002655	cutaneous Paget disease
MONDO:0002656	skin carcinoma
MONDO:0002657	breast disease
MONDO:0002658	iris cancer
MONDO:0002651	anal Paget disease
MONDO:0002652	anus adenocarcinoma
MONDO:0002653	Paget disease of the penis
MONDO:0002654	uterine disease
MONDO:0014639	familial temporal lobe epilepsy 7
MONDO:0002650	scrotal carcinoma
MONDO:0014638	Fanconi anemia complementation group T
MONDO:0014644	hereditary spastic paraplegia 74
MONDO:0014643	congenital cataract-microcephaly-nevus flammeus simplex-severe intellectual disability syndrome
MONDO:0014642	candidiasis, familial, 9
MONDO:0014641	frontotemporal dementia and/or amyotrophic lateral sclerosis 4
MONDO:0014648	Al-Raqad syndrome
MONDO:0014647	developmental and epileptic encephalopathy, 50
MONDO:0014646	Zimmermann-Laband syndrome 2
MONDO:0014645	BENTA disease
MONDO:0014640	frontotemporal dementia and/or amyotrophic lateral sclerosis 3
MONDO:0002648	mammary Paget disease
MONDO:0002649	scrotum Paget disease
MONDO:0002666	pancreatic signet ring cell adenocarcinoma
MONDO:0000003	17-hydroxysteroid dehydrogenase deficiency
MONDO:0002667	gallbladder signet ring cell adenocarcinoma
MONDO:0000002	46,XX sex reversal
MONDO:0000001	disease or disorder
MONDO:0002668	gallbladder adenocarcinoma
MONDO:0002669	ampullary signet ring cell adenocarcinoma
MONDO:0000007	atypical Mycobacteriosis, familial
MONDO:0002662	plague
MONDO:0002663	systemic mastocytosis
MONDO:0000006	alopecia-mental retardation syndrome
MONDO:0002664	extrahepatic bile duct signet ring cell carcinoma
MONDO:0000005	alopecia, isolated
MONDO:0000004	adrenocortical insufficiency
MONDO:0002665	extrahepatic bile duct adenocarcinoma
MONDO:0014629	autoimmune interstitial lung disease-arthritis syndrome
MONDO:0014628	basal ganglia calcification, idiopathic, 6
MONDO:0002660	blepharochalasis
MONDO:0002661	uveal disease
MONDO:0014627	dystonia 27
MONDO:0014633	myoclonic-atonic epilepsy
MONDO:0014632	hypomyelinating leukodystrophy 10
MONDO:0014631	hypomagnesemia, seizures, and intellectual disability
MONDO:0014630	NTHL1-related attenuated familial adenomatous polyposis
MONDO:0014637	DOCK2 deficiency
MONDO:0014636	combined oxidative phosphorylation defect type 25
MONDO:0014635	microphthalmia, isolated, with coloboma 10
MONDO:0014634	46,XY sex reversal 10
MONDO:0002659	uveal cancer
MONDO:0002633	cranial nerve neoplasm
MONDO:0002634	liposarcoma of bone
MONDO:0002635	periodontal disease
MONDO:0002636	accessory nerve disease
MONDO:0002630	small cell osteogenic sarcoma
MONDO:0002631	conventional osteosarcoma
MONDO:0002632	metachronous osteosarcoma of the bone
MONDO:0014619	trichothiodystrophy 3, photosensitive
MONDO:0014618	retinitis pigmentosa 71
MONDO:0014617	intellectual disability, autosomal dominant 38
MONDO:0014616	Skint1-like pseudogene
MONDO:0014622	isolated focal non-epidermolytic palmoplantar keratoderma
MONDO:0014621	Brugada syndrome 9
MONDO:0014620	myoclonic dystonia 26
MONDO:0014626	spinocerebellar ataxia type 41
MONDO:0014625	developmental and epileptic encephalopathy, 33
MONDO:0014624	Brown syndrome
MONDO:0014623	microcephaly 14, primary, autosomal recessive
MONDO:0002626	spinal accessory nerve neoplasm
MONDO:0002627	chondroblastic osteosarcoma
MONDO:0002628	peripheral osteosarcoma
MONDO:0002629	bone osteosarcoma
MONDO:0002644	idiopathic granulomatous myositis
MONDO:0002645	cerebritis
MONDO:0002646	viral laryngitis
MONDO:0002647	laryngitis
MONDO:0002640	optic nerve neoplasm
MONDO:0002641	subclavian artery aneurysm
MONDO:0002642	trochlear nerve neoplasm
MONDO:0002643	vestibular disease
MONDO:0014608	mandibulofacial dysostosis with alopecia
MONDO:0014607	developmental and epileptic encephalopathy, 32
MONDO:0014606	intellectual disability-microcephaly-strabismus-behavioral abnormalities syndrome
MONDO:0014605	microcephaly-corpus callosum hypoplasia-intellectual disability-facial dysmorphism syndrome
MONDO:0014609	cognitive impairment - coarse facies - heart defects - obesity - pulmonary involvement - short stature - skeletal dysplasia syndrome
MONDO:0014611	multiple mitochondrial dysfunctions syndrome 4
MONDO:0014610	ciliary dyskinesia, primary, 31
MONDO:0014615	trichothiodystrophy 2, photosensitive
MONDO:0014614	congenital stationary night blindness 1G
MONDO:0014613	pulmonary fibrosis and/or bone marrow failure, Telomere-related, 3
MONDO:0014612	pulmonary fibrosis and/or bone marrow failure, Telomere-related, 4
MONDO:0002637	histiocytosis
MONDO:0002638	glossopharyngeal nerve neoplasm
MONDO:0002639	glossopharyngeal nerve disease
MONDO:0012090	autosomal dominant nonsyndromic deafness 47
MONDO:0012091	autosomal recessive nonsyndromic deafness 32
MONDO:0012094	prostate cancer, hereditary, 4
MONDO:0012095	intellectual disability-brachydactyly-Pierre Robin syndrome
MONDO:0012092	hereditary sensory and autonomic neuropathy type 5
MONDO:0012093	prostate cancer, hereditary, 3
MONDO:0012098	spinocerebellar ataxia type 20
MONDO:0012099	AICA-ribosiduria
MONDO:0012096	Charcot-Marie-Tooth disease axonal type 2L
MONDO:0012097	spondylocostal dysostosis 2, autosomal recessive
MONDO:0000099	trichoepithelioma, multiple familial
MONDO:0012080	neuronopathy, distal hereditary motor, type 2B
MONDO:0000094	spherocytosis
MONDO:0000093	Schistosoma mansoni infection, susceptibility
MONDO:0000092	pyloric stenosis, infantile
MONDO:0000091	progressive familial heart block
MONDO:0000098	thyrotoxic periodic paralysis
MONDO:0000097	thyroid dyshormonogenesis
MONDO:0000096	pulmonary surfactant metabolism dysfunction
MONDO:0000095	split-hand/foot malformation
MONDO:0012089	ichthyosis prematurity syndrome
MONDO:0000090	progressive external ophthalmoplegia with mitochondrial DNA deletions
MONDO:0012083	autosomal dominant nonsyndromic deafness 28
MONDO:0012084	aromatic L-amino acid decarboxylase deficiency
MONDO:0012081	15q11q13 microduplication syndrome
MONDO:0012082	asperger syndrome, susceptibility to, 1
MONDO:0012087	primary ciliary dyskinesia 4
MONDO:0012088	primary ciliary dyskinesia 5
MONDO:0012085	primary ciliary dyskinesia 3
MONDO:0012086	autosomal dominant nonsyndromic deafness 31
MONDO:0012078	Joubert syndrome 3
MONDO:0012079	asperger syndrome, susceptibility to, 2
MONDO:0012072	familial partial lipodystrophy, Kobberling type
MONDO:0012073	ribose-5-P isomerase deficiency
MONDO:0012070	autosomal dominant Charcot-Marie-Tooth disease type 2G
MONDO:0012071	congenital generalized lipodystrophy type 1
MONDO:0012076	midface hypoplasia, obesity, developmental delay, and neonatal hypotonia
MONDO:0012077	amyotrophic lateral sclerosis type 8
MONDO:0012074	mandibuloacral dysplasia with type B lipodystrophy
MONDO:0012075	oligodontia-cancer predisposition syndrome
MONDO:0002699	pancreatic ductal carcinoma
MONDO:0000036	hemolytic anemia, nonspherocytic
MONDO:0000035	glucocorticoid deficiency
MONDO:0000034	glomerulopathy with fibronectin deposits
MONDO:0000033	frontonasal dysplasia
MONDO:0002695	sagittal sinus thrombosis
MONDO:0002696	Sertoli cell tumor
MONDO:0000039	hypercalciuria, absorptive
MONDO:0002697	ovarian gonadoblastoma
MONDO:0000038	hyper-IgE recurrent infection syndrome
MONDO:0002698	testicular gonadoblastoma
MONDO:0000037	herpes simplex encephalitis, susceptibility
MONDO:0002691	liver cancer
MONDO:0002692	intracranial sinus thrombosis
MONDO:0002693	lateral sinus thrombosis
MONDO:0002694	cavernous sinus thrombosis
MONDO:0000032	febrile seizures, familial
MONDO:0000031	fatty liver disease, nonalcoholic
MONDO:0000030	sleep-related hypermotor epilepsy
MONDO:0002690	meningioma
MONDO:0014688	short-rib thoracic dysplasia 14 with polydactyly
MONDO:0012025	branchiootic syndrome 3
MONDO:0014687	retinitis pigmentosa 73
MONDO:0012026	myotonia, potassium-aggravated
MONDO:0012023	autosomal dominant nonsyndromic deafness 49
MONDO:0014686	short stature, microcephaly, and endocrine dysfunction
MONDO:0012024	retinitis pigmentosa 26
MONDO:0014685	progressive myoclonic epilepsy type 9
MONDO:0012029	microcephaly 6, primary, autosomal recessive
MONDO:0012027	autoimmune disease, susceptibility to, 2
MONDO:0014689	Klippel-Feil anomaly-myopathy-facial dysmorphism syndrome
MONDO:0012028	autoimmune disease, susceptibility to, 3
MONDO:0014680	herpes simplex encephalitis, susceptibility to, 7
MONDO:0014684	combined oxidative phosphorylation defect type 26
MONDO:0012021	myopia 17, autosomal dominant
MONDO:0012022	orofacial cleft 4
MONDO:0014683	muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A9
MONDO:0014682	thyroid cancer, nonmedullary, 5
MONDO:0014681	thyroid cancer, nonmedullary, 4
MONDO:0012020	chromosome 22q11.2 microduplication syndrome
MONDO:0000047	immunodeficiency with hyper-IgM
MONDO:0000046	hypouricemia, renal
MONDO:0000045	hypothyroidism, congenital, nongoitrous
MONDO:0000044	hereditary hypophosphatemic rickets
MONDO:0000049	invasive pneumococcal disease, recurrent isolated
MONDO:0000048	immunoglobulin A deficiency
MONDO:0012009	coronary heart disease, susceptibility to, 2
MONDO:0000043	hypomagnesemia
MONDO:0000042	hyperprolinemia
MONDO:0000041	hyperphosphatasia with mental retardation syndrome
MONDO:0000040	hyperphenylalaninemia, BH4-deficient
MONDO:0012014	Charcot-Marie-Tooth disease recessive intermediate A
MONDO:0014677	achromatopsia 7
MONDO:0014676	Emery-Dreifuss muscular dystrophy 3, autosomal recessive
MONDO:0012015	nystagmus 3, congenital, autosomal dominant
MONDO:0014675	autosomal recessive nonsyndromic deafness 104
MONDO:0012012	Charcot-Marie-Tooth disease dominant intermediate C
MONDO:0012013	glaucoma-ectopia-microspherophakia-stiff joints-short stature syndrome
MONDO:0014674	maturity-onset diabetes of the young type 14
MONDO:0012018	myopathy, myosin storage, autosomal dominant
MONDO:0012019	spondyloepiphyseal dysplasia, Kimberley type
MONDO:0012016	capillary malformation-arteriovenous malformation syndrome
MONDO:0014679	polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis
MONDO:0014678	intellectual disability, autosomal dominant 39
MONDO:0012017	Parkes Weber syndrome
MONDO:0012010	coronary heart disease, susceptibility to, 4
MONDO:0014673	cataract 44
MONDO:0012011	coronary artery disease, autosomal dominant, 1
MONDO:0014672	osteogenesis imperfecta type 17
MONDO:0014671	neuropathy, hereditary motor and sensory, type 6B
MONDO:0014670	lethal congenital contracture syndrome 9
MONDO:0002677	conventional fibrosarcoma
MONDO:0000014	colorblindness, partial
MONDO:0002678	pediatric fibrosarcoma
MONDO:0000013	choroidal dystrophy
MONDO:0002679	cerebral infarction
MONDO:0000012	choreoathetosis
MONDO:0000011	chondrodysplasia
MONDO:0002673	dermatofibrosarcoma protuberans
MONDO:0000018	myotonic dystrophy
MONDO:0000017	deafness, autosomal recessive
MONDO:0002674	stricture or kinking of ureter
MONDO:0002675	neurofibrosarcoma
MONDO:0000016	coronary heart disease
MONDO:0002676	adult fibrosarcoma
MONDO:0000015	classic complement early component deficiency
MONDO:0002670	ampulla of vater adenocarcinoma
MONDO:0002671	signet ring cell breast carcinoma
MONDO:0002672	acinar prostate adenocarcinoma, signet ring variant
MONDO:0000010	cerebrooculofacioskeletal syndrome
MONDO:0014666	hypomyelinating leukodystrophy 11
MONDO:0012003	autosomal recessive nonsyndromic deafness 39
MONDO:0012004	parathyroid gland carcinoma
MONDO:0014665	Charcot-Marie-Tooth disease axonal type 2V
MONDO:0014664	Joubert syndrome 23
MONDO:0012001	mandibulofacial dysostosis with ptosis, autosomal dominant
MONDO:0012002	autosomal recessive nonsyndromic deafness 40
MONDO:0014663	Silver-Russell syndrome 3
MONDO:0012007	scimitar anomaly, multiple cardiac malformations, and craniofacial and central nervous system abnormalities
MONDO:0014669	cone-rod dystrophy 21
MONDO:0012008	Lelis syndrome
MONDO:0014668	cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 4
MONDO:0012005	growth failure, microcephaly, intellectual disability, cataracts, large joint contractures, osteoporosis, cortical dysplasia, and cerebellar atrophy
MONDO:0014667	cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 3
MONDO:0012006	craniosynostosis with ocular abnormalities and hallucal defects
MONDO:0000009	inherited bleeding disorder, platelet-type
MONDO:0000008	bare lymphocyte syndrome
MONDO:0014662	congenital insensitivity to pain-hypohidrosis syndrome
MONDO:0012000	specific phobia
MONDO:0014661	epidermolysis bullosa simplex with nail dystrophy
MONDO:0014660	microcephaly 15, primary, autosomal recessive
MONDO:0002688	duodenal obstruction
MONDO:0000025	familial cold autoinflammatory syndrome
MONDO:0002689	pseudomyxoma peritonei
MONDO:0000024	exostoses, multiple
MONDO:0000023	infantile liver failure
MONDO:0000022	nocturnal enuresis
MONDO:0002684	atypical choroid plexus papilloma
MONDO:0000029	corticosterone methyloxidase deficiency
MONDO:0002685	childhood choroid plexus carcinoma
MONDO:0000028	epilepsy, hot water
MONDO:0000027	epilepsy, absence
MONDO:0002686	mast-cell sarcoma
MONDO:0002687	superior mesenteric artery syndrome
MONDO:0000026	Fanconi renotubular syndrome
MONDO:0002680	chronic wasting disease
MONDO:0002681	choroid plexus cancer
MONDO:0002682	cerebral ventricle cancer
MONDO:0014649	intellectual disability, autosomal recessive 50
MONDO:0002683	adult choroid plexus neoplasm
MONDO:0000021	short-rib thoracic dysplasia
MONDO:0000020	elliptocytosis
MONDO:0014655	Bethlem myopathy 2
MONDO:0014654	Ullrich congenital muscular dystrophy 2
MONDO:0014653	retinitis pigmentosa 72
MONDO:0014652	exudative vitreoretinopathy 6
MONDO:0014659	infantile liver failure syndrome 2
MONDO:0014658	severe achondroplasia-developmental delay-acanthosis nigricans syndrome
MONDO:0014657	primary ciliary dyskinesia 32
MONDO:0014656	progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2
MONDO:0000019	ectodermal dysplasia
MONDO:0014651	acrofacial dysostosis Cincinnati type
MONDO:0014650	familial temporal lobe epilepsy 8
MONDO:0000079	nephrolithiasis/osteoporosis, hypophosphatemic
MONDO:0000078	acrocephalopolysyndactyly
MONDO:0000077	nystagmus
MONDO:0000072	myopathy, reducing body, X-linked
MONDO:0000071	myopathy, myofibrillar
MONDO:0000070	mycobacterium tuberculosis, susceptibility
MONDO:0000076	neuropathy, hereditary sensory and autonomic
MONDO:0000075	neuronopathy, distal hereditary motor
MONDO:0000074	neurodegeneration with brain iron accumulation
MONDO:0000073	nail disorder, nonsyndromic congenital
MONDO:0012069	keratoconus 3
MONDO:0012067	asthma-related traits, susceptibility to, 2
MONDO:0012068	brachial palsy, familial congenital
MONDO:0012061	familial sick sinus syndrome
MONDO:0012062	dilated cardiomyopathy 1O
MONDO:0012060	autosomal recessive nonsyndromic deafness 35
MONDO:0012065	Stevens-Johnson syndrome
MONDO:0012066	atrial fibrillation, familial, 1
MONDO:0012063	ulnar/fibula ray defect-brachydactyly syndrome
MONDO:0012064	choanal atresia-hearing loss-cardiac defects-craniofacial dysmorphism syndrome
MONDO:0000089	age-related hearing impairment
MONDO:0000088	precocious puberty
MONDO:0000083	Griscelli syndrome
MONDO:0000082	pelvic organ prolapse
MONDO:0000081	ovarian dysgenesis
MONDO:0000080	Oto-palato-digital syndrome
MONDO:0000087	polymicrogyria
MONDO:0000086	polydactyly, preaxial
MONDO:0000085	pituitary hormone deficiency, combined
MONDO:0000084	pigmented nodular adrenocortical disease
MONDO:0012058	myocardial infarction, susceptibility to, 2
MONDO:0012059	polydactyly, postaxial, type A4
MONDO:0012056	Leber congenital amaurosis 9
MONDO:0012057	legionnaire disease, susceptibility to
MONDO:0012050	major depressive disorder 1
MONDO:0012051	periodontitis, aggressive, 2
MONDO:0012054	schizophrenia 12
MONDO:0012055	Larsen-like osseous dysplasia-short stature syndrome
MONDO:0012052	ALG1-CDG
MONDO:0012053	aneurysm, intracranial berry, 2
MONDO:0000058	melanoma, cutaneous malignant
MONDO:0000057	medullary cystic kidney disease
MONDO:0000056	mandibuloacral dysplasia with lipodystrophy
MONDO:0000055	major affective disorder
MONDO:0000059	methylmalonic aciduria and homocystinuria
MONDO:0000050	isolated congenital growth hormone deficiency
MONDO:0000054	macular dystrophy
MONDO:0000053	macroglobulinemia, Waldenstrom
MONDO:0000052	leukodystrophy, hypomyelinating
MONDO:0000051	keratoderma, palmoplantar striate
MONDO:0012047	alopecia universalis congenita, 10Y gonadal dysgenesis, and laryngomalacia
MONDO:0012048	endogenous depression
MONDO:0012045	myopia 5, autosomal dominant
MONDO:0012046	congenital corneal opacities, cornea guttata, and corectopia
MONDO:0012049	orofaciodigital syndrome VII
MONDO:0012040	inflammatory bowel disease 9
MONDO:0012043	Reis-Bucklers corneal dystrophy
MONDO:0012044	corneal dystrophy, lattice type 3A
MONDO:0012041	MUTYH-related attenuated familial adenomatous polyposis
MONDO:0012042	hirschsprung disease, susceptibility to, 8
MONDO:0000069	multiple endocrine neoplasia
MONDO:0000068	mucolipidosis
MONDO:0000067	mitochondrial DNA depletion syndrome
MONDO:0000066	mitochondrial complex deficiency
MONDO:0000061	microcephaly, primary, autosomal recessive
MONDO:0000060	microcephalic osteodysplastic primordial dwarfism
MONDO:0000065	microvascular complications of diabetes, susceptibility
MONDO:0000064	syndromic microphthalmia
MONDO:0000063	molybdenum cofactor deficiency
MONDO:0000062	isolated microphthalmia
MONDO:0014699	intellectual disability, autosomal dominant 40
MONDO:0012036	systemic lupus erythematosus, susceptibility to, 4
MONDO:0012037	intellectual disability, autosomal recessive 3
MONDO:0014698	microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome
MONDO:0014697	immunodeficiency, common variable, 12
MONDO:0012034	autosomal dominant limb-girdle muscular dystrophy type 1F
MONDO:0012035	craniosynostosis-intracranial calcifications syndrome
MONDO:0014696	cerebrooculofacioskeletal syndrome 3
MONDO:0012038	speech-sound disorder
MONDO:0012039	myocardial infarction, susceptibility to
MONDO:0014691	Noonan syndrome 9
MONDO:0014690	dyskeratosis congenita, autosomal dominant 6
MONDO:0014695	glioma susceptibility 9
MONDO:0012032	Braddock syndrome
MONDO:0012033	bradyopsia
MONDO:0014694	spondylocostal dysostosis 6, autosomal recessive
MONDO:0012030	autosomal dominant nonsyndromic deafness 43
MONDO:0014693	Noonan syndrome 10
MONDO:0014692	retinitis pigmentosa 74
MONDO:0012031	platelet-type bleeding disorder 10
MONDO:0002501	brain glioblastoma
MONDO:0002502	giant cell glioblastoma
MONDO:0002503	adult astrocytic tumour
MONDO:0002504	grade III astrocytoma
MONDO:0002500	gliosarcoma
MONDO:0002534	fallopian tube papilloma
MONDO:0002535	verrucous papilloma
MONDO:0002536	skin papilloma
MONDO:0002537	inverted papilloma
MONDO:0002530	malignant spindle cell melanoma
MONDO:0002531	skin neoplasm
MONDO:0002532	squamous cell neoplasm
MONDO:0002533	papillary adenoma
MONDO:0014519	chronic mountain sickness, susceptibility to
MONDO:0014518	platelet-type bleeding disorder 19
MONDO:0014517	generalized epilepsy with febrile seizures plus, type 9
MONDO:0014523	juvenile-onset diabetes mellitus-central and peripheral neurodegeneration syndrome
MONDO:0014522	retinal dystrophy and obesity
MONDO:0014521	progressive myoclonic epilepsy type 7
MONDO:0014520	46,XX ovarian dysgenesis-short stature syndrome
MONDO:0014527	progeroid features-hepatocellular carcinoma predisposition syndrome
MONDO:0014526	polyglucosan body myopathy type 2
MONDO:0014525	combined oxidative phosphorylation defect type 23
MONDO:0014524	intellectual disability, autosomal recessive 47
MONDO:0002527	keratoacanthoma
MONDO:0002528	synovium neoplasm
MONDO:0002529	skin squamous cell carcinoma
MONDO:0002545	spinal cord disease
MONDO:0002546	schwannoma
MONDO:0002547	nerve sheath neoplasm
MONDO:0002548	cellular schwannoma
MONDO:0002541	spinal cord oligodendroglioma
MONDO:0002542	spinal cord glioma
MONDO:0002543	adult oligodendroglioma
MONDO:0002544	brain oligodendroglioma
MONDO:0014509	vitelliform macular dystrophy 5
MONDO:0014508	vitelliform macular dystrophy 4
MONDO:0014507	Catel-Manzke syndrome
MONDO:0014506	hypomyelinating leukodystrophy 9
MONDO:0002540	childhood oligodendroglioma
MONDO:0014512	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome due to a point mutation
MONDO:0014511	Charcot-Marie-Tooth disease axonal type 2S
MONDO:0014510	fatty acyl-CoA reductase 1 deficiency
MONDO:0014516	microcephaly and chorioretinopathy 2
MONDO:0014515	macular dystrophy with central cone involvement
MONDO:0014514	aortic aneurysm, familial thoracic 9
MONDO:0014513	nemaline myopathy 10
MONDO:0002538	progressive muscular atrophy
MONDO:0002539	oligodendroglioma
MONDO:0002512	papillary adenocarcinoma
MONDO:0002513	kidney benign neoplasm
MONDO:0002514	hepatobiliary neoplasm
MONDO:0002515	hepatobiliary disease
MONDO:0002510	germ cell and embryonal cancer
MONDO:0002511	stenosis of lacrimal sac
MONDO:0014501	macular degeneration, early-onset
MONDO:0014500	atrial conduction disease
MONDO:0014505	developmental and epileptic encephalopathy, 27
MONDO:0014504	Perrault syndrome 5
MONDO:0014503	autosomal recessive spinocerebellar ataxia 17
MONDO:0014502	mendelian susceptibility to mycobacterial diseases due to complete ISG15 deficiency
MONDO:0002509	non-specific granulomatous orchitis
MONDO:0002505	childhood astrocytic tumor
MONDO:0002506	early myoclonic encephalopathy
MONDO:0002507	gingival overgrowth
MONDO:0002508	gingivitis
MONDO:0002523	cutaneous mucinosis
MONDO:0002524	hyperlipoproteinemia type III
MONDO:0002525	inherited lipid metabolism disorder
MONDO:0002526	dermal unilateral segmental cavernous angioma
MONDO:0002520	hepatic porphyria
MONDO:0002521	multiple symmetrical lipomatosis
MONDO:0002522	tenosynovial giant cell tumor
MONDO:0002516	digestive system cancer
MONDO:0002517	tenosynovitis of foot and ankle
MONDO:0002518	gallbladder papillary neoplasm
MONDO:0002519	anus disease
MONDO:0002578	botryoid rhabdomyosarcoma
MONDO:0002579	orbit embryonal rhabdomyosarcoma
MONDO:0002574	prostate embryonal rhabdomyosarcoma
MONDO:0002575	prostate rhabdomyosarcoma
MONDO:0002576	embryonal extrahepatic bile duct rhabdomyosarcoma
MONDO:0002577	extrahepatic bile duct rhabdomyosarcoma
MONDO:0002570	high pressure neurological syndrome
MONDO:0002571	primary central nervous system lymphoma
MONDO:0002572	aspiration pneumonitis
MONDO:0002573	pleomorphic rhabdomyosarcoma
MONDO:0014567	glutamate pyruvate transaminase 2 deficiency
MONDO:0014566	Charcot-Marie-Tooth disease axonal type 2U
MONDO:0014565	cataract 43
MONDO:0014564	congenital bile acid synthesis defect 5
MONDO:0014569	lethal congenital contracture syndrome 7
MONDO:0014568	hereditary spastic paraplegia 73
MONDO:0014563	mitochondrial short-chain Enoyl-Coa hydratase 1 deficiency
MONDO:0014562	neonatal encephalomyopathy-cardiomyopathy-respiratory distress syndrome
MONDO:0014561	3-methylglutaconic aciduria with cataracts, neurologic involvement and neutropenia
MONDO:0014560	amelogenesis imperfecta type 1F
MONDO:0002589	thymoma type AB
MONDO:0002585	breast fibrocystic change, proliferative type
MONDO:0002586	thymus cancer
MONDO:0002587	encapsulated thymoma
MONDO:0002588	thymoma type A
MONDO:0002581	spindle cell rhabdomyosarcoma
MONDO:0002582	subacute leukemia
MONDO:0002583	mucinous ovarian cystadenoma
MONDO:0002584	syringomyelia
MONDO:0002580	orbit rhabdomyosarcoma
MONDO:0014556	congenital contractures of the limbs and face, hypotonia, and developmental delay
MONDO:0014555	peeling skin syndrome type A
MONDO:0014554	infantile multisystem neurologic-endocrine-pancreatic disease
MONDO:0014553	Tenorio syndrome
MONDO:0014559	progressive essential tremor-speech impairment-facial dysmorphism-intellectual disability-abnormal behavior syndrome
MONDO:0014558	autosomal dominant intellectual disability-craniofacial anomalies-cardiac defects syndrome
MONDO:0014557	ataxia - oculomotor apraxia type 4
MONDO:0014552	lethal fetal cerebrorenogenitourinary agenesis/hypoplasia syndrome
MONDO:0014551	short stature with nonspecific skeletal abnormalities
MONDO:0014550	long QT syndrome 15
MONDO:0002556	microcystic/reticular schwannoma
MONDO:0002557	schwannomatosis
MONDO:0002558	melanotic neurilemmoma
MONDO:0002559	plexiform schwannoma
MONDO:0002552	vascular myelopathy
MONDO:0002553	cerebellopontine angle tumor
MONDO:0002554	sympathetic neurilemmoma
MONDO:0002555	trigeminal schwannoma
MONDO:0002550	hypoglossal nerve neoplasm
MONDO:0014539	focal segmental glomerulosclerosis 9
MONDO:0002551	c-P angle neurinoma
MONDO:0014545	progressive myoclonic epilepsy type 8
MONDO:0014544	osteogenesis imperfecta type 16
MONDO:0014543	congenital myasthenic syndrome 14
MONDO:0014542	congenital myasthenic syndrome 15
MONDO:0014549	lethal congenital contracture syndrome 6
MONDO:0014548	long QT syndrome 14
MONDO:0014547	combined oxidative phosphorylation defect type 24
MONDO:0014546	myopathy due to calsequestrin and SERCA1 protein overload
MONDO:0014541	motor developmental delay due to 14q32.2 paternally expressed gene defect
MONDO:0002549	schwannoma of twelfth cranial nerve
MONDO:0014540	amelogenesis imperfecta type 1H
MONDO:0002567	tracheal disease
MONDO:0002568	tracheal stenosis
MONDO:0002569	gastric dilatation
MONDO:0002563	jejunal somatostatinoma
MONDO:0002564	jejunal neoplasm
MONDO:0002565	myelitis
MONDO:0002566	complex regional pain syndrome
MONDO:0002560	junctional epidermolysis bullosa
MONDO:0002561	lysosomal storage disease
MONDO:0014529	cerebellar-facial-dental syndrome
MONDO:0002562	demyelinating disease
MONDO:0014528	chronic atrial and intestinal dysrhythmia
MONDO:0014534	lissencephaly 6 with microcephaly
MONDO:0014533	developmental and epileptic encephalopathy, 28
MONDO:0014532	autosomal dominant mitochondrial myopathy with exercise intolerance
MONDO:0014531	amyotrophic lateral sclerosis type 22
MONDO:0014538	fibrosis of extraocular muscles, congenital, 5
MONDO:0014537	nephronophthisis 19
MONDO:0014536	thrombocytopenia 5
MONDO:0014535	hyperproinsulinemia
MONDO:0014530	autosomal recessive spinocerebellar ataxia 18
MONDO:0014599	intellectual disability, autosomal dominant 34
MONDO:0014598	developmental and epileptic encephalopathy, 31
MONDO:0014597	immunodeficiency 39
MONDO:0014592	microcephaly and chorioretinopathy 3
MONDO:0014591	autosomal dominant Robinow syndrome 2
MONDO:0014590	congenital myasthenic syndrome 18
MONDO:0014596	lissencephaly 7 with cerebellar hypoplasia
MONDO:0014595	developmental and epileptic encephalopathy, 30
MONDO:0014594	autosomal dominant nonsyndromic deafness 67
MONDO:0014593	developmental and epileptic encephalopathy, 29
MONDO:0002596	chordoma
MONDO:0002597	notochordal tumor
MONDO:0002598	germinoma
MONDO:0002599	teratocarcinoma
MONDO:0002592	invasive malignant thymoma
MONDO:0002593	thymic carcinoma
MONDO:0002594	monkeypox
MONDO:0002595	vaccinia
MONDO:0002590	combined thymoma
MONDO:0002591	dendritic cell thymoma
MONDO:0014589	maturity-onset diabetes of the young type 13
MONDO:0014588	congenital myasthenic syndrome 11
MONDO:0014587	congenital myasthenic syndrome 9
MONDO:0014586	congenital myasthenic syndrome 4B
MONDO:0014581	congenital myasthenic syndrome 2A
MONDO:0014580	intellectual disability, autosomal dominant 33
MONDO:0014585	congenital myasthenic syndrome 3C
MONDO:0014584	congenital myasthenic syndrome 3B
MONDO:0014583	congenital myasthenic syndrome 3A
MONDO:0014582	congenital myasthenic syndrome 2C
MONDO:0014578	congenital myasthenic syndrome 17
MONDO:0014577	short-rib thoracic dysplasia 13 with or without polydactyly
MONDO:0014576	lipoyl transferase 1 deficiency
MONDO:0014575	Singleton-Merten syndrome 2
MONDO:0014579	Senior-Loken syndrome 8
MONDO:0014570	lethal congenital contracture syndrome 8
MONDO:0014574	peeling skin-leukonuchia-acral punctate keratoses-cheilitis-knuckle pads syndrome
MONDO:0014573	Cole-Carpenter syndrome 2
MONDO:0014572	Lichtenstein-Knorr syndrome
MONDO:0014571	optic atrophy 9
MONDO:0002413	glycogen storage disease I
MONDO:0002414	gastric hemangioma
MONDO:0002415	bone carcinoma
MONDO:0002416	ethmoid sinus squamous cell carcinoma
MONDO:0002410	pyeloureteritis cystica
MONDO:0002411	narcissistic personality disorder
MONDO:0002412	glycogen storage disease
MONDO:0014402	severe neurodegenerative syndrome with lipodystrophy
MONDO:0014401	tall stature-scoliosis-macrodactyly of the great toes syndrome
MONDO:0014400	retinitis pigmentosa 70
MONDO:0014406	pancreatic agenesis 2
MONDO:0014405	STING-associated vasculopathy with onset in infancy
MONDO:0014404	Webb-Dattani syndrome
MONDO:0014403	short stature due to GHSR deficiency
MONDO:0002406	dermatitis
MONDO:0002407	capillary hemangioma
MONDO:0002408	hereditary hyperbilirubinemia
MONDO:0002409	auditory system disease
MONDO:0002424	rectosigmoid carcinoma
MONDO:0002425	rectosigmoid junction cancer
MONDO:0002426	lung sarcoma
MONDO:0002427	cerebellar disease
MONDO:0002420	tic disorder
MONDO:0002421	chorioangioma
MONDO:0002422	adamantinoma
MONDO:0002423	rectosigmoid junction neoplasm
MONDO:0002417	ethmoid sinus adenoid cystic carcinoma
MONDO:0002418	ethmoid sinus adenocarcinoma
MONDO:0002419	transient tic disorder
MONDO:0002402	malignant giant cell tumor
MONDO:0002403	synovium cancer
MONDO:0002404	liver hemangioma
MONDO:0002405	hepatic vascular disease
MONDO:0002400	synovitis
MONDO:0002401	malignant tenosynovial giant cell tumor
MONDO:0014499	intellectual disability, autosomal recessive 46
MONDO:0014498	familial cold autoinflammatory syndrome 4
MONDO:0014493	autoimmune lymphoproliferative syndrome due to CTLA4 haploinsuffiency
MONDO:0014492	woolly hair-palmoplantar keratoderma syndrome
MONDO:0014491	immunodeficiency 37
MONDO:0014490	ketoacidosis due to monocarboxylate transporter-1 deficiency
MONDO:0014497	polyendocrine-polyneuropathy syndrome
MONDO:0014496	mitochondrial complex III deficiency nuclear type 9
MONDO:0014495	retinitis pigmentosa-juvenile cataract-short stature-intellectual disability syndrome
MONDO:0014494	psoriasis 15, pustular, susceptibility to
MONDO:0002457	Treacher-Collins syndrome
MONDO:0002458	acute pancreatitis
MONDO:0002459	type IV hypersensitivity disease
MONDO:0002453	retrocochlear disease
MONDO:0002454	thyroid adenoma
MONDO:0002455	exocervical carcinoma
MONDO:0026426	X inactivation, familial skewed, 2
MONDO:0002456	cervix carcinoma
MONDO:0002450	prostatic adenoma
MONDO:0002451	benign prostate phyllodes tumor
MONDO:0002452	prostate leiomyoma
MONDO:0014446	Bardet-Biedl syndrome 18
MONDO:0014445	Bardet-Biedl syndrome 17
MONDO:0014444	Bardet-Biedl syndrome 16
MONDO:0014443	Bardet-Biedl syndrome 15
MONDO:0014449	congenital analbuminemia
MONDO:0014448	hyperthyroxinemia, familial dysalbuminemic
MONDO:0014447	Bardet-Biedl syndrome 19
MONDO:0014442	Bardet-Biedl syndrome 14
MONDO:0014441	Bardet-Biedl syndrome 13
MONDO:0014440	Bardet-Biedl syndrome 12
MONDO:0002468	hyperimmunoglobulin syndrome
MONDO:0002469	lacrimal gland carcinoma ex pleomorphic adenoma
MONDO:0002464	lacrimal gland cancer
MONDO:0002465	bronchiolitis
MONDO:0002466	eye carcinoma
MONDO:0002467	inner ear disease
MONDO:0002460	lacrimal system cancer
MONDO:0002461	membranoproliferative glomerulonephritis
MONDO:0002462	glomerulonephritis
MONDO:0014429	autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency
MONDO:0002463	lacrimal gland carcinoma
MONDO:0014435	Bardet-Biedl syndrome 7
MONDO:0014434	Bardet-Biedl syndrome 5
MONDO:0014433	Bardet-Biedl syndrome 4
MONDO:0014432	Bardet-Biedl syndrome 2
MONDO:0014439	Bardet-Biedl syndrome 11
MONDO:0014438	Bardet-Biedl syndrome 10
MONDO:0014437	Bardet-Biedl syndrome 9
MONDO:0014436	Bardet-Biedl syndrome 8
MONDO:0014431	LIPE-related familial partial lipodystrophy
MONDO:0014430	intellectual disability, autosomal recessive 45
MONDO:0002435	oculomotor nerve neoplasm
MONDO:0002436	nasal disorder
MONDO:0002437	dehydration polycythemia
MONDO:0002438	acquired polycythemia
MONDO:0002431	nonspecific interstitial pneumonia
MONDO:0002432	malignant neoplasm of acoustic nerve
MONDO:0026404	X inactivation, familial skewed, 1
MONDO:0002433	malignant cranial nerve neoplasm
MONDO:0002434	oculomotor nerve cancer
MONDO:0014419	ataxia - intellectual disability - oculomotor apraxia - cerebellar cysts syndrome
MONDO:0002430	acute interstitial pneumonia
MONDO:0014418	myopathy, centronuclear, 5
MONDO:0014424	congenital deficiency in alpha-fetoprotein
MONDO:0014423	severe combined immunodeficiency due to DNA-PKcs deficiency
MONDO:0014422	vesicoureteral reflux 8
MONDO:0014421	glucocorticoid resistance
MONDO:0014428	autosomal recessive nonsyndromic deafness 102
MONDO:0014427	cone-rod dystrophy 20
MONDO:0014426	nanophthalmos 4
MONDO:0014425	hereditary persistence of alpha-fetoprotein
MONDO:0002428	protozoa infectious disease
MONDO:0014420	short stature due to primary acid-labile subunit deficiency
MONDO:0002429	idiopathic interstitial pneumonia
MONDO:0002446	hemoglobinopathy
MONDO:0002447	endometrial carcinoma
MONDO:0002448	laryngeal sarcoma
MONDO:0002449	nodular degeneration of cornea
MONDO:0002442	long QT syndrome
MONDO:0002443	bruxism
MONDO:0002444	melancholia
MONDO:0002445	hemoglobin c disease
MONDO:0014409	intellectual disability, autosomal recessive 44
MONDO:0002440	erythropoietin polycythemia
MONDO:0014408	megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 3
MONDO:0014407	megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 2
MONDO:0002441	Jervell and Lange-Nielsen syndrome
MONDO:0014413	orofaciodigital syndrome type 14
MONDO:0014412	hyperlipoproteinemia, type 1D
MONDO:0014411	myopia 24, autosomal dominant
MONDO:0014410	spinocerebellar ataxia type 37
MONDO:0014417	spinocerebellar ataxia type 38
MONDO:0014416	ACTH-independent macronodular adrenal hyperplasia 2
MONDO:0014415	kallikrein, decreased urinary activity of
MONDO:0014414	STAT3-related early-onset multisystem autoimmune disease
MONDO:0002439	stress polycythemia
MONDO:0002497	food allergy
MONDO:0002498	glioblastoma multiforme
MONDO:0002499	astrocytoma
MONDO:0002493	prostatic acinar adenocarcinoma
MONDO:0002494	substance-related disorder
MONDO:0002495	colon signet ring cell adenocarcinoma
MONDO:0002496	submucosal invasive colon adenocarcinoma
MONDO:0002490	breast sarcoma
MONDO:0002491	substance abuse
MONDO:0002492	acute kidney failure
MONDO:0014489	limb-girdle muscular dystrophy due to POMK deficiency
MONDO:0014488	diabetes mellitus, noninsulin-dependent, 5
MONDO:0014487	congenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay syndrome
MONDO:0014482	intellectual disability, autosomal dominant 29
MONDO:0014481	inflammatory skin and bowel disease, neonatal, 2
MONDO:0014480	46,XY sex reversal 9
MONDO:0014486	intellectual disability, autosomal dominant 30
MONDO:0014485	pontocerebellar hypoplasia, type 1C
MONDO:0014484	microcephaly 12, primary, autosomal recessive
MONDO:0014483	retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies
MONDO:0014479	porokeratosis 8, disseminated superficial actinic type
MONDO:0014478	mirror movements 3
MONDO:0014477	developmental and epileptic encephalopathy, 26
MONDO:0014476	episodic ataxia type 8
MONDO:0014471	mitochondrial proton-transporting ATP synthase complex deficiency
MONDO:0014470	autosomal dominant nonsyndromic deafness 65
MONDO:0014475	spinocerebellar ataxia type 40
MONDO:0014474	autosomal recessive limb-girdle muscular dystrophy type 2U
MONDO:0014473	microcephaly 13, primary, autosomal recessive
MONDO:0014472	periodic fever-infantile enterocolitis-autoinflammatory syndrome
MONDO:0002479	Sertoli-Leydig cell tumor
MONDO:0002475	lacrimal gland adenocarcinoma
MONDO:0002476	anuria
MONDO:0002477	prostate neuroendocrine neoplasm
MONDO:0002478	mixed germ cell-sex cord-stromal tumor
MONDO:0002471	bursitis
MONDO:0002472	carcinoma ex pleomorphic adenoma
MONDO:0002473	cystic kidney disease
MONDO:0002474	primary hyperoxaluria
MONDO:0002470	photosensitive trichothiodystrophy
MONDO:0014468	congenital myasthenic syndrome 7
MONDO:0014467	Charcot-Marie-Tooth disease recessive intermediate D
MONDO:0014466	Neu-Laxova syndrome 2
MONDO:0014465	primary ciliary dyskinesia 30
MONDO:0014469	autosomal recessive nonsyndromic deafness 103
MONDO:0014460	nail and teeth abnormalities-marginal palmoplantar keratoderma-oral hyperpigmentation syndrome
MONDO:0014464	progressive encephalopathy with leukodystrophy due to DECR deficiency
MONDO:0014463	microcephaly, short stature, and impaired glucose metabolism
MONDO:0014462	focal segmental glomerulosclerosis 8
MONDO:0014461	hypogonadotropic hypogonadism 22 with or without anosmia
MONDO:0002486	lobular neoplasia
MONDO:0002487	breast granular cell tumor
MONDO:0002488	intraductal breast neoplasm
MONDO:0002489	malignant breast phyllodes tumor
MONDO:0002482	nipple neoplasm
MONDO:0002483	breast myoepithelial tumor
MONDO:0002484	breast ductal carcinoma
MONDO:0002485	breast neuroendocrine neoplasm
MONDO:0002480	endometrioid tumor
MONDO:0002481	ovarian neuroendocrine neoplasm
MONDO:0014457	hyperphosphatasia with intellectual disability syndrome 5
MONDO:0014456	autosomal recessive severe congenital neutropenia due to JAGN1 deficiency
MONDO:0014455	cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome
MONDO:0014454	Hennekam lymphangiectasia-lymphedema syndrome 2
MONDO:0014459	Adams-Oliver syndrome 5
MONDO:0014458	Fanconi renotubular syndrome 4 with maturity-onset diabetes of the young
MONDO:0014453	immunodeficiency 36
MONDO:0014452	familial dysfibrinogenemia
MONDO:0014451	focal segmental glomerulosclerosis 7
MONDO:0014450	breasts and/or nipples, aplasia or hypoplasia of, 2
MONDO:0004911	cardiovascular syphilis
MONDO:0004910	mitral valve prolapse
MONDO:0004913	alternating esotropia
MONDO:0004912	muscular dystrophy
MONDO:0016900	partial deletion of the long arm of chromosome 1
MONDO:0016901	partial deletion of the long arm of chromosome 2
MONDO:0016902	partial deletion of the long arm of chromosome 3
MONDO:0016903	partial deletion of the long arm of chromosome 4
MONDO:0004908	galactosemia
MONDO:0004907	alopecia
MONDO:0004909	urethral gland abscess
MONDO:0004904	toxic maculopathy
MONDO:0004903	deep keratitis
MONDO:0004906	hereditary fructose intolerance syndrome
MONDO:0004905	intestinal disaccharidase deficiency
MONDO:0004922	developmental coordination disorder
MONDO:0004921	Omsk hemorrhagic fever
MONDO:0004924	chronic canaliculitis
MONDO:0004923	chronic inflammation of lacrimal passage
MONDO:0004920	hydrocele
MONDO:0004919	infected hydrocele
MONDO:0004918	central corneal ulcer
MONDO:0004914	celiac artery stenosis from compression by median arcuate ligament of diaphragm
MONDO:0004917	internal hordeolum
MONDO:0004900	peripheral vertigo
MONDO:0004902	interstitial keratitis
MONDO:0004901	lingual-facial-buccal dyskinesia
MONDO:0004955	metabolic syndrome
MONDO:0004954	malt lymphoma
MONDO:0004957	mucinous adenocarcinoma
MONDO:0004956	metastatic prostate carcinoma
MONDO:0004951	susceptibility to HIV infection
MONDO:0004950	gastric carcinoma
MONDO:0004953	invasive ductal breast carcinoma
MONDO:0004952	Hodgkins lymphoma
MONDO:0016937	partial duplication of chromosome 19
MONDO:0016938	partial trisomy of chromosome 20
MONDO:0016939	partial duplication of the short arm of chromosome 2
MONDO:0016944	partial duplication of the short arm of chromosome 7
MONDO:0016945	partial duplication of the short arm of chromosome 8
MONDO:0016946	partial trisomy of the short arm of chromosome 9
MONDO:0016947	partial duplication of the short arm of chromosome 10
MONDO:0016940	partial duplication of the short arm of chromosome 3
MONDO:0016941	partial duplication of the short arm of chromosome 4
MONDO:0016942	partial trisomy/tetrasomy of the short arm of chromosome 5
MONDO:0016943	partial duplication of the short arm of chromosome 6
MONDO:0004948	B-cell chronic lymphocytic leukemia
MONDO:0004947	B-cell acute lymphoblastic leukemia
MONDO:0004949	neoplasm of mature B-cells
MONDO:0002303	central retinal vein occlusion
MONDO:0004966	gastritis
MONDO:0004965	acinar cell carcinoma
MONDO:0002304	protein S deficiency
MONDO:0004968	acute myelomonocytic leukemia
MONDO:0002305	thrombophilia
MONDO:0004967	acute lymphoblastic leukemia
MONDO:0002306	angular blepharoconjunctivitis
MONDO:0004962	stage II endometrioid carcinoma
MONDO:0002300	dermis tumor
MONDO:0004961	stage I endometrioid carcinoma
MONDO:0002301	frontal sinus squamous cell carcinoma
MONDO:0004964	peripheral T-cell lymphoma, not otherwise specified
MONDO:0004963	T-cell acute lymphoblastic leukemia
MONDO:0002302	acromegaly
MONDO:0004960	monoclonal gammopathy
MONDO:0016926	Geleophysic dysplasia
MONDO:0016927	partial duplication of chromosome 6
MONDO:0016928	partial duplication of chromosome 7
MONDO:0016929	partial duplication of chromosome 8
MONDO:0016933	partial trisomy/tetrasomy of the short arm of chromosome 12
MONDO:0016934	partial duplication of chromosome 16
MONDO:0016935	partial duplication of chromosome 17
MONDO:0016936	partial trisomy/tetrasomy of chromosome 18
MONDO:0016930	partial trisomy/tetrasomy of chromosome 9
MONDO:0016931	partial duplication of chromosome 10
MONDO:0016932	partial duplication of chromosome 11
MONDO:0004959	plasma cell neoplasm
MONDO:0004958	oral cavity squamous cell carcinoma
MONDO:0004933	hypoplastic left heart syndrome
MONDO:0004932	null-cell leukemia
MONDO:0004935	acquired carotenemia
MONDO:0004934	periostitis
MONDO:0004931	residual stage corticosteroid-induced glaucoma
MONDO:0004930	steroid-induced glaucoma
MONDO:0016919	partial deletion of the long arm of chromosome 21
MONDO:0016915	partial deletion of the long arm of chromosome 17
MONDO:0016916	partial deletion of the long arm of chromosome 18
MONDO:0016917	partial deletion of the long arm of chromosome 19
MONDO:0016918	partial deletion of the long arm of chromosome 20
MONDO:0016922	partial duplication of chromosome 2
MONDO:0016923	partial duplication of chromosome 3
MONDO:0016924	partial duplication of chromosome 4
MONDO:0016925	partial trisomy/tetrasomy of chromosome 5
MONDO:0016920	partial deletion of the long arm of chromosome 22
MONDO:0016921	partial duplication of chromosome 1
MONDO:0004929	constant exophthalmos
MONDO:0004926	dacryocystitis
MONDO:0004925	chronic dacryocystitis
MONDO:0004928	lymph node disease
MONDO:0004927	dacryocystocele
MONDO:0004944	neurosyphilis
MONDO:0004943	orbit sarcoma
MONDO:0004946	hypoglycemia
MONDO:0004945	hypereosinophilic syndrome
MONDO:0004940	acute female pelvic peritonitis
MONDO:0004942	orbit lymphoma
MONDO:0004941	eosinophilia-myalgia syndrome
MONDO:0016908	partial monosomy of the long arm of chromosome 9
MONDO:0016909	partial monosomy of the long arm of chromosome 10
MONDO:0016904	partial deletion of the long arm of chromosome 5
MONDO:0016905	partial deletion of the long arm of chromosome 6
MONDO:0016906	partial deletion of the long arm of chromosome 7
MONDO:0016907	partial deletion of the long arm of chromosome 8
MONDO:0016911	partial deletion of the long arm of chromosome 13
MONDO:0016912	partial deletion of the long arm of chromosome 14
MONDO:0016913	partial deletion of the long arm of chromosome 15
MONDO:0016914	partial deletion of the long arm of chromosome 16
MONDO:0016910	partial deletion of the long arm of chromosome 11
MONDO:0004937	hypervitaminosis D
MONDO:0004936	uterine inversion
MONDO:0004939	hallucinogen dependence
MONDO:0004938	substance dependence
MONDO:0014390	hypotrichosis 13
MONDO:0014399	ataxia-telangiectasia-like disorder 2
MONDO:0014394	Diamond-Blackfan anemia 13
MONDO:0014393	lymphatic malformation 4
MONDO:0014392	developmental and epileptic encephalopathy, 25
MONDO:0014391	severe combined immunodeficiency due to CTPS1 deficiency
MONDO:0014398	combined oxidative phosphorylation defect type 21
MONDO:0014397	combined oxidative phosphorylation defect type 20
MONDO:0014396	dilated cardiomyopathy 1NN
MONDO:0014395	frontotemporal dementia and/or amyotrophic lateral sclerosis 2
MONDO:0002398	mucinous adenofibroma
MONDO:0002399	tenosynovial giant cell tumor, localized type
MONDO:0002394	Leydig cell tumor
MONDO:0002395	renal adenoma
MONDO:0002396	nephrogenic adenofibroma
MONDO:0002397	liver sarcoma
MONDO:0002390	ossifying fibromyxoid tumor
MONDO:0002391	skin sarcoma
MONDO:0002392	lymphangiosarcoma
MONDO:0014389	polyglucosan body myopathy 1 with or without immunodeficiency
MONDO:0014388	familial median cleft of the upper and lower lips
MONDO:0014383	myopathy, tubular aggregate, 2
MONDO:0014382	tall stature-intellectual disability-facial dysmorphism syndrome
MONDO:0014381	cholestasis, progressive familial intrahepatic, 4
MONDO:0014380	colobomatous microphthalmia-rhizomelic dysplasia syndrome
MONDO:0014387	leukoencephalopathy, progressive, with ovarian failure
MONDO:0014386	platelet-type bleeding disorder 18
MONDO:0014385	amelogenesis imperfecta hypomaturation type 2A5
MONDO:0014384	hypotrichosis 12
MONDO:0014379	ADNP-related multiple congenital anomalies - intellectual disability - autism spectrum disorder
MONDO:0014378	primary ciliary dyskinesia 29
MONDO:0014377	developmental and epileptic encephalopathy, 24
MONDO:0014372	cone-rod dystrophy 19
MONDO:0014371	developmental and epileptic encephalopathy, 23
MONDO:0014370	pontocerebellar hypoplasia type 2E
MONDO:0014376	intellectual disability, autosomal dominant 27
MONDO:0014375	congenital diarrhea 7 with exudative enteropathy
MONDO:0014374	nephronophthisis 18
MONDO:0014373	nephrotic syndrome, type 10
MONDO:0041996	thallium poisoning
MONDO:0002336	inflammatory and toxic neuropathy
MONDO:0004999	chondrosarcoma
MONDO:0002337	intra-abdominal hemangioma
MONDO:0004998	chondromyxoid fibroma
MONDO:0002338	extratemporal epilepsy
MONDO:0002339	hemangioma
MONDO:0002332	splenic disease
MONDO:0004995	cardiovascular disease
MONDO:0004994	cardiomyopathy
MONDO:0002333	splenic abscess
MONDO:0004997	chondroblastoma
MONDO:0002334	hematopoietic and lymphoid system neoplasm
MONDO:0004996	childhood acute myeloid leukemia
MONDO:0002335	chronic inflammatory demyelinating polyneuritis
MONDO:0004991	minimally invasive lung adenocarcinoma
MONDO:0004990	breast tumor luminal A or B
MONDO:0002330	alcoholic psychosis
MONDO:0004993	carcinoma
MONDO:0004992	cancer
MONDO:0002331	nephrosis
MONDO:0014319	renal hypodysplasia/aplasia 2
MONDO:0014325	pachyonychia congenita 4
MONDO:0016988	hyperinsulinism due to HNF4A deficiency
MONDO:0014324	pachyonychia congenita 3
MONDO:0016989	Fuchs heterochromic iridocyclitis
MONDO:0014323	retinitis pigmentosa 68
MONDO:0014322	premature ovarian failure 9
MONDO:0014329	atrial standstill 2
MONDO:0016984	nevus of Ota
MONDO:0016985	nevus of Ito
MONDO:0014328	developmental and epileptic encephalopathy, 19
MONDO:0014327	palmoplantar keratoderma, nonepidermolytic, focal or diffuse
MONDO:0016986	congenital smooth muscle hamartoma
MONDO:0014326	nemaline myopathy 9
MONDO:0016987	neuroacanthocytosis
MONDO:0016980	ATR-X-related syndrome
MONDO:0016981	infantile spams-psychomotor retardation-progressive brain atrophy-basal ganglia disease syndrome
MONDO:0016982	angiosarcoma
MONDO:0016983	Bartter syndrome with hypocalcemia
MONDO:0002329	testicular disease
MONDO:0014321	premature ovarian failure 8
MONDO:0014320	optic atrophy-intellectual disability syndrome
MONDO:0002347	barbiturate dependence
MONDO:0002348	chondrodysplasia punctata
MONDO:0002349	agammaglobulinemia
MONDO:0002343	splenic hemangioma
MONDO:0002344	corneal dystrophy
MONDO:0002345	cervicitis
MONDO:0002346	malignant histiocytic disease
MONDO:0002340	tactile epilepsy
MONDO:0002341	granulomatous angiitis
MONDO:0014309	obesity due to CEP19 deficiency
MONDO:0002342	chondromalacia
MONDO:0014308	familial temporal lobe epilepsy 6
MONDO:0014314	sacral agenesis-abnormal ossification of the vertebral bodies-persistent notochordal canal syndrome
MONDO:0016977	moderately-differentiated thymic neuroendocrine carcinoma
MONDO:0014313	autosomal recessive primary immunodeficiency with defective spontaneous natural killer cell cytotoxicity
MONDO:0016978	poorly differentiated thymic neuroendocrine carcinoma
MONDO:0016979	MRCS syndrome
MONDO:0014312	auriculocondylar syndrome 3
MONDO:0014311	autosomal recessive spinocerebellar ataxia 15
MONDO:0014318	hyperphosphatasia with intellectual disability syndrome 4
MONDO:0016973	thymoma type A
MONDO:0016974	thymoma type B
MONDO:0014317	pancytopenia-developmental delay syndrome
MONDO:0014316	Alzheimer disease 19
MONDO:0016975	thymoma type AB
MONDO:0016976	well-differentiated thymic neuroendocrine carcinoma
MONDO:0014315	Mitchell-Riley syndrome
MONDO:0016970	partial trisomy of the long arm of chromosome 20
MONDO:0016971	limb-girdle muscular dystrophy
MONDO:0016972	partial duplication of the long arm of chromosome 22
MONDO:0014310	hereditary sclerosing poikiloderma with tendon and pulmonary involvement
MONDO:0004977	angioimmunoblastic T-cell lymphoma
MONDO:0002314	chronic conjunctivitis
MONDO:0004976	amyotrophic lateral sclerosis
MONDO:0002315	hereditary spastic paraplegia
MONDO:0004979	asthma
MONDO:0002316	motor peripheral neuropathy
MONDO:0004978	aortic stenosis
MONDO:0002317	central nervous system origin vertigo
MONDO:0002310	anterior dislocation of lens
MONDO:0004973	adenosquamous lung carcinoma
MONDO:0002311	retinal vascular disease
MONDO:0004972	adenoma
MONDO:0004975	Alzheimer disease
MONDO:0002312	opportunistic mycosis
MONDO:0002313	vernal conjunctivitis
MONDO:0004974	adrenal gland pheochromocytoma
MONDO:0004971	adenoid cystic carcinoma
MONDO:0004970	adenocarcinoma
MONDO:0016959	partial duplication of the long arm of chromosome 8
MONDO:0014303	hereditary spastic paraplegia 64
MONDO:0016966	partial trisomy of the long arm of chromosome 16
MONDO:0016967	partial duplication of the long arm of chromosome 17
MONDO:0014302	hereditary spastic paraplegia 62
MONDO:0016968	partial trisomy of the long arm of chromosome 18
MONDO:0014301	dowling-degos disease 3
MONDO:0016969	partial duplication of the long arm of chromosome 19
MONDO:0014300	proximal myopathy with extrapyramidal signs
MONDO:0016962	partial duplication of the long arm of chromosome 11
MONDO:0014307	Dowling-Degos disease 4
MONDO:0014306	vasculitis due to ADA2 deficiency
MONDO:0016963	partial duplication of the long arm of chromosome 13
MONDO:0014305	hereditary spastic paraplegia 63
MONDO:0016964	partial duplication of the long arm of chromosome 14
MONDO:0014304	hereditary spastic paraplegia 61
MONDO:0016965	partial duplication of the long arm of chromosome 15
MONDO:0016960	partial trisomy of the long arm of chromosome 9
MONDO:0016961	partial duplication of the long arm of chromosome 10
MONDO:0041959	fibrosis of bile duct
MONDO:0002307	blepharoconjunctivitis
MONDO:0004969	acute quadriplegic myopathy
MONDO:0002308	giant papillary conjunctivitis
MONDO:0002309	papillary conjunctivitis
MONDO:0002325	tooth erosion, non-bacterial
MONDO:0004988	breast adenocarcinoma
MONDO:0004987	urinary bladder neoplasm
MONDO:0002326	alcohol-induced mental disorder
MONDO:0002327	intracranial cavernous angioma
MONDO:0004989	breast carcinoma
MONDO:0002328	intracranial hemangioma
MONDO:0004984	basal-like breast carcinoma
MONDO:0002321	sensory peripheral neuropathy
MONDO:0002322	angiodysplasia
MONDO:0004983	azoospermia
MONDO:0004986	urinary bladder carcinoma
MONDO:0002323	cherry hemangioma
MONDO:0004985	bipolar disorder
MONDO:0002324	enamel erosion
MONDO:0004980	atopic eczema
MONDO:0004982	pancreatitis
MONDO:0004981	atrial fibrillation
MONDO:0002320	congenital nervous system disorder
MONDO:0016948	partial duplication of the short arm of chromosome 11
MONDO:0016949	partial duplication of the short arm of chromosome 16
MONDO:0016955	partial duplication of the long arm of chromosome 4
MONDO:0016956	partial trisomy of the long arm of chromosome 5
MONDO:0016957	partial duplication of the long arm of chromosome 6
MONDO:0016958	partial duplication of the long arm of chromosome 7
MONDO:0016951	partial trisomy/tetrasomy of the short arm of chromosome 18
MONDO:0016952	partial duplication of the long arm of chromosome 1
MONDO:0016953	partial duplication of the long arm of chromosome 2
MONDO:0016954	partial duplication of the long arm of chromosome 3
MONDO:0016950	partial duplication of the short arm of chromosome 17
MONDO:0002318	trachea leiomyoma
MONDO:0002319	phosphorus metabolism disease
MONDO:0002376	spleen angiosarcoma
MONDO:0002377	breast intracanalicular fibroadenoma
MONDO:0002378	dermoid cyst
MONDO:0002379	cystic teratoma
MONDO:0002372	ovarian monodermal and highly specialized teratoma
MONDO:0002373	benign mesothelioma
MONDO:0002374	parachordoma
MONDO:0002375	sebaceous adenoma
MONDO:0002370	ovarian Brenner tumor
MONDO:0002371	breast pericanalicular fibroadenoma
MONDO:0014369	postaxial polydactyly-anterior pituitary anomalies-facial dysmorphism syndrome
MONDO:0014368	melanoma, cutaneous malignant, susceptibility to, 10
MONDO:0014367	Aicardi-Goutieres syndrome 7
MONDO:0014366	spermatogenic failure 14
MONDO:0014361	autism spectrum disorder due to AUTS2 deficiency
MONDO:0014360	developmental and epileptic encephalopathy, 21
MONDO:0014365	spermatogenic failure 13
MONDO:0014364	mitochondrial complex III deficiency nuclear type 8
MONDO:0014363	autosomal recessive nonsyndromic deafness 101
MONDO:0014362	chromosome 16 inversion, 0.45-Mb
MONDO:0002387	liver angiosarcoma
MONDO:0002388	intracystic papillary adenoma
MONDO:0002389	adenofibroma
MONDO:0002383	Pacinian tumor
MONDO:0002384	transitional cell carcinoma
MONDO:0002385	benign cystic nephroma
MONDO:0002386	mixed epithelial stromal tumor of the kidney
MONDO:0002380	myoepithelial tumor
MONDO:0002381	sweat gland neoplasm
MONDO:0002382	benign mesenchymoma
MONDO:0014358	AHDC1-related intellectual disability - obstructive sleep apnea - mild dysmorphism syndrome
MONDO:0014357	intellectual disability, autosomal dominant 24
MONDO:0014356	mitochondrial complex III deficiency nuclear type 7
MONDO:0041903	gonococcal infection of joint
MONDO:0014355	cardiomyopathy, dilated, with woolly hair, keratoderma, and tooth agenesis
MONDO:0014359	pigmented nodular adrenocortical disease, primary, 4
MONDO:0014350	Seckel syndrome 8
MONDO:0014354	intellectual disability, autosomal recessive 43
MONDO:0014353	PGM3-CDG
MONDO:0014352	abdominal obesity-metabolic syndrome 3
MONDO:0014351	pontocerebellar hypoplasia type 9
MONDO:0002358	laryngeal carcinoma
MONDO:0002359	periosteal chondroma
MONDO:0002354	benign laryngeal neoplasm
MONDO:0002355	glottis carcinoma
MONDO:0002356	pancreas disease
MONDO:0002357	hepatic flexure cancer
MONDO:0002350	familial nephrotic syndrome
MONDO:0002351	glottis cancer
MONDO:0002352	larynx cancer
MONDO:0002353	glottis neoplasm
MONDO:0014347	short stature with microcephaly and distinctive facies
MONDO:0014346	white sponge nevus 2
MONDO:0014345	retinitis pigmentosa 69
MONDO:0014344	congenital heart defects, multiple types, 4
MONDO:0014349	pontocerebellar hypoplasia type 10
MONDO:0014348	intellectual disability, autosomal recessive 42
MONDO:0014343	Desbuquois dysplasia 2
MONDO:0014342	female infertility due to zona pellucida defect
MONDO:0014341	complex cortical dysplasia with other brain malformations 6
MONDO:0014340	atrial fibrillation, familial, 15
MONDO:0002369	cystadenoma
MONDO:0002365	kidney hemangiopericytoma
MONDO:0002366	autonomic nervous system neoplasm
MONDO:0002367	kidney cancer
MONDO:0002368	papillary serous cystadenocarcinoma
MONDO:0002361	transverse colon cancer
MONDO:0002362	serous surface papilloma
MONDO:0002363	papilloma
MONDO:0002364	Wolffian duct adenoma
MONDO:0002360	chondroma
MONDO:0014336	intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency
MONDO:0016999	X chromosome number anomaly
MONDO:0014335	diffuse cerebral and cerebellar atrophy - intractable seizures - progressive microcephaly syndrome
MONDO:0014334	severe combined immunodeficiency due to LCK deficiency
MONDO:0014333	polymicrogyria, bilateral perisylvian, autosomal recessive
MONDO:0016995	familial multiple meningioma
MONDO:0014339	autosomal recessive spinocerebellar ataxia 16
MONDO:0016996	NK-cell enteropathy
MONDO:0014338	IL21-related infantile inflammatory bowel disease
MONDO:0016997	hereditary epidermolysis bullosa associated with ocular features
MONDO:0014337	complex cortical dysplasia with other brain malformations 5
MONDO:0016998	complex chromosomal rearrangement
MONDO:0016991	acute necrotizing encephalopathy of childhood
MONDO:0016992	peeling skin syndrome type B
MONDO:0016993	generalized peeling skin syndrome type C
MONDO:0016994	microcephalic osteodysplastic primordial dwarfism types I and III
MONDO:0014332	hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency
MONDO:0014331	Moyamoya disease with early-onset achalasia
MONDO:0014330	eculizumab, poor response to
MONDO:0016990	acquired prothrombin deficiency
MONDO:0004801	unilateral hypoactive labyrinth
MONDO:0004800	chronic dacryoadenitis
MONDO:0004803	disseminated eosinophilic collagen disease
MONDO:0004802	pulmonary eosinophilia
MONDO:0004834	ischemic fasciitis
MONDO:0004833	plantar fasciitis
MONDO:0004836	intravascular fasciitis
MONDO:0004835	necrotizing fasciitis
MONDO:0004830	fasciitis
MONDO:0004832	esophagus leiomyoma
MONDO:0004831	proliferative fasciitis
MONDO:0016816	Leigh syndrome with nephrotic syndrome
MONDO:0016817	Meier-Gorlin syndrome
MONDO:0016818	Mikati-Najjar-Sahli syndrome
MONDO:0016819	Moebius syndrome-axonal neuropathy-hypogonadotropic hypogonadism syndrome
MONDO:0016823	mycetoma
MONDO:0016824	infantile myofibromatosis
MONDO:0016825	mitochondrial myopathy-lactic acidosis-deafness syndrome
MONDO:0016826	methylmalonic acidemia with homocystinuria
MONDO:0016820	Moyamoya disease
MONDO:0016821	shoulder and girdle defects-familial intellectual disability syndrome
MONDO:0016822	myalgia-eosinophilia syndrome associated with tryptophan
MONDO:0004827	esophagus squamous cell papilloma
MONDO:0004826	urethral calculus
MONDO:0004829	Krukenberg carcinoma
MONDO:0004828	lower urinary tract calculus
MONDO:0004845	aphthous stomatitis
MONDO:0004844	oral mucosa leukoplakia
MONDO:0004847	senile cataract
MONDO:0004846	placental abruption
MONDO:0004841	kidney hypertrophy
MONDO:0004840	non-congenital cyst of kidney
MONDO:0004843	pathologic nystagmus
MONDO:0004842	stomatitis
MONDO:0016809	spinocerebellar ataxia with epilepsy
MONDO:0016805	isolated oxidative phosphorylation complex disorder
MONDO:0016806	maternally-inherited mitochondrial dystonia
MONDO:0016807	pure mitochondrial myopathy
MONDO:0016808	mitochondrial DNA depletion syndrome, hepatocerebral form
MONDO:0016812	dopa-responsive dystonia
MONDO:0016813	microsporidiosis
MONDO:0016814	maternally-inherited Leigh syndrome
MONDO:0016815	Leigh syndrome with leukodystrophy
MONDO:0016810	autosomal recessive progressive external ophthalmoplegia
MONDO:0016811	renal tubulopathy-encephalopathy-liver failure syndrome
MONDO:0004838	orthostatic proteinuria
MONDO:0004837	neurofibroma of the esophagus
MONDO:0004839	neurofibroma
MONDO:0004812	acute dacryoadenitis
MONDO:0004811	simple chronic conjunctivitis
MONDO:0004814	vascular skin disease
MONDO:0004813	tuberculous pneumothorax
MONDO:0004810	acute ethmoiditis
MONDO:0016801	mitochondrial substrate carrier disorder
MONDO:0016802	mitochondrial protein import disorder
MONDO:0016803	unspecified inborn mitochondrial disorder
MONDO:0016804	exercise intolerance with lactic acidosis
MONDO:0016800	mitochondrial membrane transport disorder
MONDO:0004809	cannabis abuse
MONDO:0004808	benign mammary dysplasia
MONDO:0004805	leukocyte disease
MONDO:0004804	dacryoadenitis
MONDO:0004807	Loeffler syndrome
MONDO:0004806	chronic eosinophilic pneumonia
MONDO:0004823	dextrocardia
MONDO:0004822	bronchiectasis
MONDO:0004825	encephalitis
MONDO:0004824	neonatal candidiasis
MONDO:0004821	nasopharyngeal disease
MONDO:0004820	peripheral nerve schwannoma
MONDO:0004819	indolent plasma cell myeloma
MONDO:0004816	refractory plasma cell neoplasm
MONDO:0004815	osteosclerotic plasma cell myeloma
MONDO:0004818	benign neurilemmoma
MONDO:0004817	non-secretory plasma cell myeloma
MONDO:0002299	glomangioma
MONDO:0014280	immunodeficiency 19
MONDO:0002295	skin glomus tumor
MONDO:0002296	glomus tumor
MONDO:0002297	epidermal appendage tumor
MONDO:0002298	cutaneous glomangioma
MONDO:0002291	cutaneous granular cell tumor
MONDO:0002292	granular cell tumor
MONDO:0002293	cutaneous ganglioneuroma
MONDO:0002294	gangliocytoma
MONDO:0002290	clitoris cancer
MONDO:0014289	macrocephaly-developmental delay syndrome
MONDO:0014284	short-rib thoracic dysplasia 10 with or without polydactyly
MONDO:0014283	autosomal dominant nonsyndromic deafness 56
MONDO:0014282	hereditary spastic paraplegia 72
MONDO:0014281	cholangiocarcinoma, susceptibility to
MONDO:0014288	Joubert syndrome 21
MONDO:0014287	short-rib thoracic dysplasia 11 with or without polydactyly
MONDO:0014286	neuropathy, hereditary sensory, type 1F
MONDO:0014285	congenital dyserythropoietic anemia type type 1B
MONDO:0014279	arrhythmogenic right ventricular dysplasia, familial, 13
MONDO:0014278	immunodeficiency 18
MONDO:0014273	microcephaly-thin corpus callosum-intellectual disability syndrome
MONDO:0014272	palmoplantar keratoderma, Nagashima type
MONDO:0014271	STT3B-CDG
MONDO:0014270	STT3A-CDG
MONDO:0014277	developmental dysplasia of the hip 2
MONDO:0014276	combined immunodeficiency due to CD3gamma deficiency
MONDO:0014275	Fanconi renotubular syndrome 3
MONDO:0014274	L-ferritin deficiency
MONDO:0002277	arteriosclerosis disorder
MONDO:0002278	benign colon neoplasm
MONDO:0002279	iron metabolism disease
MONDO:0002273	plasma protein metabolism disease
MONDO:0002274	monoclonal paraproteinemia disease
MONDO:0002275	generalized atherosclerosis
MONDO:0002276	arteriosclerotic cardiovascular disease
MONDO:0002270	viral gastritis
MONDO:0002271	colon adenocarcinoma
MONDO:0002272	polyclonal hypergammaglobulinemia
MONDO:0014269	combined oxidative phosphorylation deficiency 19
MONDO:0014268	combined immunodeficiency due to OX40 deficiency
MONDO:0014267	severe combined immunodeficiency due to IKK2 deficiency
MONDO:0014262	Rienhoff syndrome
MONDO:0014261	growth and developmental delay-hypotonia-vision impairment-lactic acidosis syndrome
MONDO:0014260	immunodeficiency, common variable, 10
MONDO:0014266	age related macular degeneration 15
MONDO:0014265	Alzheimer disease 18
MONDO:0014264	otosclerosis 10
MONDO:0014263	8q24.3 microdeletion syndrome
MONDO:0002288	ovarian cancer
MONDO:0002289	iris disease
MONDO:0002284	gangliosidosis
MONDO:0002285	pupil disease
MONDO:0002286	renal artery disease
MONDO:0002287	glandular cystitis
MONDO:0002280	anemia
MONDO:0002281	macrocytic anemia
MONDO:0002282	West Nile fever
MONDO:0002283	neuroaxonal dystrophy
MONDO:0014259	neuronopathy, distal hereditary motor, type 2D
MONDO:0014258	congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome
MONDO:0014257	nephrotic syndrome, type 9
MONDO:0014256	retinitis pigmentosa 67
MONDO:0014251	melioidosis, susceptibility to
MONDO:0014250	familial hyperprolactinemia
MONDO:0014255	complement factor b deficiency
MONDO:0014254	otofaciocervical syndrome 2
MONDO:0014253	autoimmune lymphoproliferative syndrome type 3
MONDO:0014252	familial hypobetalipoproteinemia 1
MONDO:0041879	staphylococcus aureus pneumonia
MONDO:0014291	autosomal dominant nonsyndromic deafness 54
MONDO:0014290	neurodegeneration with brain iron accumulation 6
MONDO:0014295	hereditary spastic paraplegia 57
MONDO:0014294	chromosome 15q11.2 deletion syndrome
MONDO:0014293	autosomal dominant nonsyndromic deafness 58
MONDO:0014292	leukoencephalopathy with mild cerebellar ataxia and white matter edema
MONDO:0014299	schwannomatosis 2
MONDO:0014298	chromosome 5q12 deletion syndrome
MONDO:0014297	Joubert syndrome 22
MONDO:0014296	Warburg micro syndrome 4
MONDO:0004878	female breast upper-outer quadrant cancer
MONDO:0002215	atypical teratoid rhabdoid tumor
MONDO:0002216	brain sarcoma
MONDO:0004877	transient neonatal thrombocytopenia
MONDO:0002217	central nervous system sarcoma
MONDO:0002218	temporal lobe cancer
MONDO:0004879	senile atrophy of choroid
MONDO:0002211	B cell deficiency
MONDO:0004874	ganglion or cyst of synovium/tendon/bursa
MONDO:0002212	pneumonic tularemia
MONDO:0004873	internal hemorrhoid
MONDO:0002213	tularemia
MONDO:0004876	myocardial stunning
MONDO:0004875	xanthogranulomatous cholecystitis
MONDO:0002214	brain germinoma
MONDO:0004870	diabetic neuropathy
MONDO:0004872	hemorrhoid
MONDO:0002210	vulva squamous cell carcinoma
MONDO:0004871	perianal hematoma
MONDO:0014204	basal ganglia calcification, idiopathic, 5
MONDO:0016867	partial deletion of chromosome 2
MONDO:0014203	primary ciliary dyskinesia 25
MONDO:0016868	partial deletion of chromosome 3
MONDO:0016869	partial deletion of chromosome 4
MONDO:0014202	primary ciliary dyskinesia 24
MONDO:0014201	developmental and epileptic encephalopathy, 18
MONDO:0014208	Charcot-Marie-Tooth disease type 2R
MONDO:0016863	Okihiro syndrome due to 20q13 microdeletion
MONDO:0014207	age related macular degeneration 14
MONDO:0016864	Okihiro syndrome due to a point mutation
MONDO:0014206	severe early-onset pulmonary alveolar proteinosis due to MARS deficiency
MONDO:0016865	Kleefstra syndrome due to a point mutation
MONDO:0014205	severe feeding difficulties-failure to thrive-microcephaly due to ASXL3 deficiency syndrome
MONDO:0016866	partial deletion of chromosome 1
MONDO:0016860	familial adenomatous polyposis due to 5q22.2 microdeletion
MONDO:0016861	Alagille syndrome due to 20p12 microdeletion
MONDO:0016862	Alagille syndrome due to a JAG1 point mutation
MONDO:0014200	aldosterone-producing adenoma with seizures and neurological abnormalities
MONDO:0002208	vulva adenocarcinoma
MONDO:0002209	heel spur
MONDO:0004889	total central choroidal atrophy
MONDO:0002226	tuberculous oophoritis
MONDO:0002227	ovarian lymphoma
MONDO:0004888	partial circumpapillary choroid dystrophy
MONDO:0002228	malignant ovarian surface epithelial-stromal neoplasm
MONDO:0002229	ovarian epithelial tumor
MONDO:0002222	urethra leiomyoma
MONDO:0004885	choroidal sclerosis
MONDO:0004884	eye degenerative disease
MONDO:0002223	ovarian malignant mesothelioma
MONDO:0002224	malignant ovarian cyst
MONDO:0004887	polyarteritis nodosa
MONDO:0002225	ovarian sarcoma
MONDO:0004886	diffuse secondary choroid atrophy
MONDO:0004881	myositis fibrosa
MONDO:0004880	bowel dysfunction
MONDO:0002220	tooth hard tissue disease
MONDO:0004883	hereditary choroidal atrophy
MONDO:0002221	urethral urothelial papilloma
MONDO:0004882	angioid streaks of choroid
MONDO:0016849	Nakajo-Nishimura syndrome
MONDO:0016856	Mowat-Wilson syndrome due to a ZEB2 point mutation
MONDO:0016857	blepharophimosis-epicanthus inversus-ptosis due to 3q23 rearrangement syndrome
MONDO:0041825	bacterial meningitis caused by gram-negative bacteria
MONDO:0016858	blepharophimosis-epicanthus inversus-ptosis due to a point mutation syndrome
MONDO:0016859	blepharophimosis-epicanthus inversus-ptosis due to copy number variations
MONDO:0016852	paternal uniparental disomy of chromosome X
MONDO:0016853	ring chromosome Y
MONDO:0016854	49,XXXYY syndrome
MONDO:0016855	Mowat-Wilson syndrome due to monosomy 2q22
MONDO:0016850	atypical Norrie disease due to monosomy Xp11.3
MONDO:0016851	maternal uniparental disomy of chromosome X
MONDO:0002219	paraurethral gland neoplasm
MONDO:0004856	rosacea conjunctivitis
MONDO:0004855	tenosynovitis
MONDO:0004858	occlusion of gallbladder
MONDO:0004857	tendinitis
MONDO:0004852	gonococcal keratitis
MONDO:0004851	toxic myocarditis
MONDO:0004854	ophthalmia neonatorum
MONDO:0004853	gonococcal endophthalmia
MONDO:0004850	yellow fever
MONDO:0016838	16q24.3 microdeletion syndrome
MONDO:0016839	distal 17p13.3 microdeletion syndrome
MONDO:0016845	21q22.11q22.12 microdeletion syndrome
MONDO:0016846	distal 22q11.2 microduplication syndrome
MONDO:0016847	trisomy 1q
MONDO:0016848	juvenile temporal arteritis
MONDO:0016841	20p12.3 microdeletion syndrome
MONDO:0016842	paternal 20q13.2q13.3 microdeletion syndrome
MONDO:0016843	20q13.33 microdeletion syndrome
MONDO:0016844	trisomy 20p
MONDO:0016840	trisomy 17p
MONDO:0004849	pulmonary emphysema
MONDO:0004848	ulcerative stomatitis
MONDO:0002204	transient arthritis
MONDO:0004867	upper respiratory tract disease
MONDO:0004866	eustachian tube disease
MONDO:0002205	vulvar melanoma
MONDO:0002206	sweat gland cancer
MONDO:0004869	pelvic varices
MONDO:0004868	biliary tract disease
MONDO:0002207	vulval Paget disease
MONDO:0004863	purulent endophthalmitis
MONDO:0002200	eccrine mixed tumor of skin
MONDO:0004862	vitreous abscess
MONDO:0002201	vulvar trichoepithelioma
MONDO:0002202	outlet dysfunction constipation
MONDO:0004865	blue drum syndrome
MONDO:0002203	constipation disorder
MONDO:0004864	acute allergic mucoid otitis media
MONDO:0004861	ophthalmia nodosa
MONDO:0041850	pneumonia caused by gram negative bacteria
MONDO:0004860	vitreous disease
MONDO:0016827	myopathy-growth delay-intellectual disability-hypospadias syndrome
MONDO:0016828	autosomal recessive sideroblastic anemia
MONDO:0016829	familial visceral myopathy
MONDO:0016834	16p11.2p12.2 microduplication syndrome
MONDO:0016835	14q11.2 microduplication syndrome
MONDO:0016836	16p13.11 microdeletion syndrome
MONDO:0016837	16p13.11 microduplication syndrome
MONDO:0016830	Emery-Dreifuss muscular dystrophy
MONDO:0016831	linear verrucous nevus syndrome
MONDO:0016832	distal 7q11.23 microduplication syndrome
MONDO:0016833	14q12 microdeletion syndrome
MONDO:0004859	hydrops of gallbladder
MONDO:0002259	gonadal disease
MONDO:0002255	hypertrophic elongation of cervix
MONDO:0002256	cervix disease
MONDO:0002257	ankylosis
MONDO:0002258	pharyngitis
MONDO:0002251	hepatitis
MONDO:0002252	granulomatous hepatitis
MONDO:0002253	spondylosis
MONDO:0002254	syndromic disease
MONDO:0002250	basilar artery insufficiency
MONDO:0014248	autism spectrum disorder - epilepsy - arthrogryposis syndrome
MONDO:0014247	familial episodic pain syndrome with predominantly lower limb involvement
MONDO:0014246	episodic pain syndrome, familial, 2
MONDO:0014245	Diamond-Blackfan anemia 12
MONDO:0014249	multiple fibroadenoma of the breast
MONDO:0014240	periventricular nodular heterotopia 6
MONDO:0014244	hereditary sensory and autonomic neuropathy type 7
MONDO:0014243	Schaaf-Yang syndrome
MONDO:0014242	van Maldergem syndrome 2
MONDO:0014241	leukemia, acute lymphoblastic, susceptibility to, 3
MONDO:0002266	malt worker's lung
MONDO:0002267	obstructive lung disease
MONDO:0002268	dyspepsia
MONDO:0002269	gastroenteritis
MONDO:0002262	capillary lymphangioma
MONDO:0002263	female reproductive system disease
MONDO:0002264	atrophy of prostate
MONDO:0002265	stereotypic movement disorder
MONDO:0002260	hidradenitis
MONDO:0002261	keratopathy
MONDO:0014237	autosomal recessive nonsyndromic deafness 76
MONDO:0014236	Ehlers-Danlos syndrome, musculocontractural type 2
MONDO:0014235	chromosome 22q13 duplication syndrome
MONDO:0014234	reticulate acropigmentation of Kitamura
MONDO:0016896	partial deletion of the short arm of chromosome 18
MONDO:0016897	partial deletion of the short arm of chromosome 19
MONDO:0016898	partial monosomy of the short arm of chromosome 20
MONDO:0014239	testicular anomalies with or without congenital heart disease
MONDO:0014238	severe intellectual disability-short stature-behavioral abnormalities-facial dysmorphism syndrome
MONDO:0016899	Duchenne and Becker muscular dystrophy
MONDO:0016892	partial deletion of the short arm of chromosome 10
MONDO:0016893	partial deletion of the short arm of chromosome 11
MONDO:0016894	partial deletion of the short arm of chromosome 16
MONDO:0016895	partial monosomy of the short arm of chromosome 17
MONDO:0014233	early-onset Parkinson disease 20
MONDO:0014232	craniosynostosis 5, susceptibility to
MONDO:0014231	juvenile onset Parkinson disease 19A
MONDO:0016890	partial deletion of the short arm of chromosome 8
MONDO:0016891	partial deletion of the short arm of chromosome 9
MONDO:0014230	candidiasis, familial, 8
MONDO:0002237	carbuncle
MONDO:0002238	ascending colon cancer
MONDO:0004899	monofixation syndrome
MONDO:0002239	post-surgical hypoinsulinemia
MONDO:0002233	enamel caries
MONDO:0004896	esotropia
MONDO:0002234	vaginitis
MONDO:0004895	accommodative esotropia
MONDO:0004898	total circumpapillary dystrophy of choroid
MONDO:0002235	eyelid neoplasm
MONDO:0004897	hypotropia
MONDO:0002236	ocular cancer
MONDO:0004892	refractive error
MONDO:0002230	ovarian Wilms tumor
MONDO:0004891	hyperopia
MONDO:0002231	malignant ovarian germ cell neoplasm
MONDO:0004894	cyclotropia
MONDO:0002232	nasal cavity disease
MONDO:0004893	hypertropia
MONDO:0004890	partial central choroid dystrophy
MONDO:0014226	idiopathic CD4 lymphocytopenia
MONDO:0016889	partial deletion of the short arm of chromosome 7
MONDO:0014225	hemochromatosis type 5
MONDO:0014224	developmental delay with autism spectrum disorder and gait instability
MONDO:0014223	amyotrophic lateral sclerosis type 19
MONDO:0016885	partial deletion of the short arm of chromosome 3
MONDO:0016886	partial deletion of the short arm of chromosome 4
MONDO:0014229	microphthalmia, syndromic 12
MONDO:0016887	partial deletion of the short arm of chromosome 5
MONDO:0014228	corneal dystrophy, Fuchs endothelial, 8
MONDO:0014227	hypopigmentation-punctate palmoplantar keratoderma syndrome
MONDO:0016888	partial deletion of the short arm of chromosome 6
MONDO:0016881	partial deletion of chromosome 19
MONDO:0016882	partial deletion of chromosome 20
MONDO:0016883	partial deletion of the short arm of chromosome 1
MONDO:0016884	partial deletion of the short arm of chromosome 2
MONDO:0014222	immunodeficiency 14
MONDO:0014221	triosephosphate isomerase deficiency
MONDO:0014220	myopathy due to myoadenylate deaminase deficiency
MONDO:0016880	partial deletion of chromosome 18
MONDO:0002248	myeloproliferative neoplasm
MONDO:0002249	thrombocytosis disease
MONDO:0002244	factor VII deficiency
MONDO:0002245	blood platelet disease
MONDO:0002246	perichondritis of auricle
MONDO:0002247	factor X deficiency
MONDO:0002240	acute perichondritis of pinna
MONDO:0002241	factor XIII deficiency
MONDO:0002242	coagulation protein disease
MONDO:0014209	early-onset progressive neurodegeneration-blindness-ataxia-spasticity syndrome
MONDO:0002243	hemorrhagic disease
MONDO:0014215	primary ciliary dyskinesia 27
MONDO:0016878	partial deletion of chromosome 16
MONDO:0014214	short-rib thoracic dysplasia 8 with or without polydactyly
MONDO:0016879	partial deletion of chromosome 17
MONDO:0014213	intellectual disability-feeding difficulties-developmental delay-microcephaly syndrome
MONDO:0014212	sulfite oxidase deficiency due to molybdenum cofactor deficiency type C
MONDO:0014219	alacrima, achalasia, and intellectual disability syndrome
MONDO:0016874	partial deletion of chromosome 9
MONDO:0016875	partial deletion of chromosome 10
MONDO:0014218	severe dermatitis-multiple allergies-metabolic wasting syndrome
MONDO:0014217	telangiectasia, hereditary hemorrhagic, type 5
MONDO:0016876	partial deletion of chromosome 11
MONDO:0014216	primary ciliary dyskinesia 28
MONDO:0016877	partial deletion of the long arm of chromosome 12
MONDO:0016870	partial deletion of chromosome 5
MONDO:0016871	partial deletion of chromosome 6
MONDO:0016872	partial deletion of chromosome 7
MONDO:0016873	partial deletion of chromosome 8
MONDO:0014211	primary ciliary dyskinesia 26
MONDO:0041806	drug-resistant tuberculosis
MONDO:0014210	intellectual disability-hypotonia-spasticity-sleep disorder syndrome
MONDO:0022586	bone dysplasia Moore type
MONDO:0022587	bone dysplasia corpus callosum agenesis
MONDO:0022580	blepharo naso facial syndrome van Maldergem type
MONDO:0022572	bilateral renal agenesis dominant type
MONDO:0022573	biliary atresia intrahepatic non syndromic form
MONDO:0022574	biliary atresia intrahepatic syndromic form
MONDO:0022575	biliary hypoplasia
MONDO:0022576	bilirubin induced brain injury in the newborn
MONDO:0022577	Billet bear syndrome
MONDO:0022578	childhood bladder carcinoma
MONDO:0010594	inherited genitourinary tract anomalies
MONDO:0010593	Frontometaphyseal dysplasia
MONDO:0010596	membranoproliferative glomerulonephritis, X-linked
MONDO:0010595	Sertoli cell-only syndrome
MONDO:0010598	glycogen storage disease IXa1
MONDO:0010597	glutamyl ribose-5-phosphate storage disease
MONDO:0010599	granulomas, congenital cerebral
MONDO:0010590	FG syndrome 1
MONDO:0010592	focal dermal hypoplasia
MONDO:0010591	fingerprint body myopathy
MONDO:0022566	BEST1 retinopathy
MONDO:0022567	bhaskar jagannathan syndrome
MONDO:0022568	bidirectional tachycardia
MONDO:0010579	X-linked corneal dermoid
MONDO:0009589	mesomelic dwarfism-cleft palate-camptodactyly syndrome
MONDO:0009588	Langer mesomelic dysplasia
MONDO:0009587	mesoaxial hexadactyly and cardiac malformation
MONDO:0009586	mesangial sclerosis, diffuse renal, with ocular abnormalities
MONDO:0009585	encephalopathy due to beta-mercaptolactate-cysteine disulfiduria
MONDO:0009584	intellectual disability, Buenos-Aires type
MONDO:0022560	benign metastasizing leiomyoma
MONDO:0009583	blepharophimosis - intellectual disability syndrome, Ohdo type
MONDO:0010583	Dyggve-Melchior-Clausen syndrome, X-linked
MONDO:0009582	Mietens syndrome
MONDO:0010582	diabetes insipidus, neurohypophyseal type, X-linked inheritance
MONDO:0009581	intellectual disability-dysmorphism-hypogonadism-diabetes mellitus syndrome
MONDO:0010585	X-linked hypohidrotic ectodermal dysplasia
MONDO:0009580	intellectual disability, autosomal recessive 1
MONDO:0010584	dyskeratosis congenita, X-linked
MONDO:0010587	epidermodysplasia verruciformis, X-linked
MONDO:0010586	X-linked Ehlers-Danlos syndrome
MONDO:0010589	Aarskog-Scott syndrome, X-linked
MONDO:0010588	exudative vitreoretinopathy 2, X-linked
MONDO:0022559	benign angiitis of the central nervous system
MONDO:0010581	diabetes insipidus, nephrogenic, X-linked
MONDO:0010580	immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome
MONDO:0022551	Basedow's coma
MONDO:0022552	Bazopoulou Kyrkanidou syndrome
MONDO:0022553	BD syndrome
MONDO:0022555	Beardwell syndrome
MONDO:0022556	oculo-cerebral dysplasia
MONDO:0022557	behrens baumann dust syndrome
MONDO:0010569	X-linked complicated corpus callosum dysgenesis
MONDO:0010568	Aicardi syndrome
MONDO:0009599	metaphyseal dysostosis-intellectual disability-conductive deafness syndrome
MONDO:0009598	metaphyseal chondrodysplasia-retinitis pigmentosa syndrome
MONDO:0009597	metaphyseal chondrodysplasia, Spahr type
MONDO:0009596	metaphyseal chondrodysplasia, Pena type
MONDO:0009595	cartilage-hair hypoplasia
MONDO:0009594	metaphyseal chondrodysplasia, Kaitila type
MONDO:0010572	occipital horn syndrome
MONDO:0010571	otopalatodigital syndrome type 2
MONDO:0009593	spondylometaphyseal dysplasia, Sedaghatian type
MONDO:0009592	metaphyseal acroscyphodysplasia
MONDO:0010574	syndromic X-linked intellectual disability 5
MONDO:0009591	metachromatic leukodystrophy, juvenile form
MONDO:0010573	cutis verticis gyrata, thyroid aplasia, and intellectual disability
MONDO:0010576	X-linked mixed deafness with perilymphatic gusher
MONDO:0009590	metachromatic leukodystrophy due to saposin b deficiency
MONDO:0010575	deafness-hypogonadism syndrome
MONDO:0010578	deafness dystonia syndrome
MONDO:0010577	deafness, X-linked 1
MONDO:0010570	craniofrontonasal syndrome
MONDO:0022598	brachydactyly absence of distal phalanges
MONDO:0022599	brachydactyly anonychia
MONDO:0009529	pyruvate dehydrogenase E3 deficiency
MONDO:0022500	arthrogryposis multiplex congenita CNS calcification
MONDO:0009528	chylomicron retention disease
MONDO:0009527	lipase deficiency, combined
MONDO:0009526	fibular aplasia, tibial campomelia, and oligosyndactyly syndrome
MONDO:0009525	split hand-foot malformation 3
MONDO:0010514	combined immunodeficiency due to moesin deficiency
MONDO:0009524	intellectual disability-spasticity-ectrodactyly syndrome
MONDO:0010513	intellectual disability, X-linked, syndromic, Borck type
MONDO:0009523	Lichtenstein syndrome
MONDO:0010516	midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis
MONDO:0009522	Leukomelanoderma-infantilism-intellectual disability-hypodontia-hypotrichosis syndrome
MONDO:0010515	Meester-Loeys syndrome
MONDO:0010518	Wiskott-Aldrich syndrome
MONDO:0009521	leukemia, acute myelocytic, with polyposis coli and colon cancer
MONDO:0010517	ciliary dyskinesia, primary, 36, X-linked
MONDO:0009520	3-hydroxy-3-methylglutaric aciduria
MONDO:0010519	alpha thalassemia-X-linked intellectual disability syndrome
MONDO:0010521	amelogenesis imperfecta type 1E
MONDO:0010520	X-linked Alport syndrome
MONDO:0010523	X-linked reticulate pigmentary disorder
MONDO:0010522	X-linked amelogenesis imperfecta hypoplastic/hypomaturation 2
MONDO:0009539	lymphoblastic leukemia, acute, with lymphomatous features
MONDO:0009538	lymphoid system deterioration, progressive
MONDO:0009537	lymphoid interstitial pneumonia
MONDO:0010503	Bartter disease type 5
MONDO:0009536	chronic mucocutaneous candidiasis due to intrinsic defect in lymphoblastic transformation
MONDO:0010502	intellectual disability, X-linked 99, syndromic, female-restricted
MONDO:0009535	lymphedema, congenital recessive
MONDO:0010505	intellectual disability-balding-patella luxation-acromicria syndrome
MONDO:0009534	chronic mucocutaneous candidiasis due to inhibition of lymphoblastic transformation
MONDO:0009533	Dahlberg-Borer-Newcomer syndrome
MONDO:0010504	immunodeficiency 47
MONDO:0010507	Xq25 microduplication syndrome
MONDO:0009532	Miller-Dieker lissencephaly syndrome
MONDO:0010506	intellectual disability, X-linked 61
MONDO:0009531	lip prints
MONDO:0009530	lipoid proteinosis
MONDO:0010509	intellectual disability, X-linked 104
MONDO:0010508	intellectual disability, X-linked 103
MONDO:0010510	intellectual disability, X-linked 105
MONDO:0010512	intellectual disability, X-linked, syndromic, bain type
MONDO:0010511	vas deferens, congenital bilateral aplasia of, X-linked
MONDO:0009509	Landau-Kleffner syndrome
MONDO:0009508	Lambotte syndrome
MONDO:0009507	Lambert syndrome
MONDO:0009506	specific granule deficiency
MONDO:0009505	lactic aciduria due to D-lactic acid
MONDO:0009504	mitochondrial DNA depletion syndrome 9
MONDO:0009503	pyruvate dehydrogenase E3-binding protein deficiency
MONDO:0009502	pyruvate dehydrogenase E2 deficiency
MONDO:0009501	metabolic myopathy due to lactate transporter defect
MONDO:0009500	kuru, susceptibility to
MONDO:0010501	syndromic X-linked intellectual disability 34
MONDO:0010500	intellectual disability, X-linked, syndromic 33
MONDO:0009519	letterer-Siwe disease
MONDO:0009518	leprosy, susceptibility to, 3
MONDO:0009517	Donohue syndrome
MONDO:0009516	absence deformity of leg-cataract syndrome
MONDO:0009515	Norum disease
MONDO:0009514	Laurence-Moon syndrome
MONDO:0009513	laryngo-onycho-cutaneous syndrome
MONDO:0009512	lethal Larsen-like syndrome
MONDO:0009511	Larsen-like syndrome, B3GAT3 type
MONDO:0009510	Laron syndrome with immunodeficiency
MONDO:0022545	Barnicoat Baraitser syndrome
MONDO:0022546	basal cell nevus anodontia abnormal bone mineralization
MONDO:0009569	Hennekam-Beemer syndrome
MONDO:0010558	choroideremia-deafness-obesity syndrome
MONDO:0010557	choroideremia
MONDO:0009568	mast syndrome
MONDO:0009567	Marinesco-Sjogren syndrome
MONDO:0010559	MASA syndrome
MONDO:0009566	marfanoid habitus-autosomal recessive intellectual disability syndrome
MONDO:0009565	microcephaly-glomerulonephritis-marfanoid habitus syndrome
MONDO:0009564	Marden-Walker syndrome
MONDO:0009563	maple syrup urine disease
MONDO:0009562	beta-mannosidosis
MONDO:0009561	alpha-mannosidosis
MONDO:0010561	Coffin-Lowry syndrome
MONDO:0010560	cleft palate with or without ankyloglossia, X-linked
MONDO:0009560	oculotrichoanal syndrome
MONDO:0010563	blue cone monochromacy
MONDO:0010562	colonic atresia
MONDO:0010565	red color blindness
MONDO:0010564	red-green color blindness
MONDO:0010567	cone dystrophy, X-linked, with tapetal-like sheen
MONDO:0010566	X-linked cone-rod dystrophy 1
MONDO:0022538	leukoplakia of gingiva
MONDO:0022535	autonomic facial cephalgia
MONDO:0010547	X-linked progressive cerebellar ataxia
MONDO:0009579	Frank-Ter Haar syndrome
MONDO:0010546	central incisors, absence of
MONDO:0010549	Charcot-Marie-Tooth disease X-linked dominant 1
MONDO:0009578	neurocutaneous melanocytosis
MONDO:0009577	megalocornea-intellectual disability syndrome
MONDO:0010548	spinocerebellar ataxia, X-linked 2
MONDO:0009576	megalocornea
MONDO:0009575	thiamine-responsive megaloblastic anemia syndrome
MONDO:0009574	megalencephaly with dysmyelination
MONDO:0009573	megaepiphyseal dwarfism
MONDO:0009572	autosomal recessive familial Mediterranean fever
MONDO:0010550	Charcot-Marie-Tooth disease X-linked recessive 2
MONDO:0009571	Meckel syndrome, type 1
MONDO:0010552	Charcot-Marie-Tooth peroneal muscular atrophy, X-linked, with aplasia cutis congenita
MONDO:0009570	McDonough syndrome
MONDO:0010551	Charcot-Marie-Tooth disease X-linked recessive 3
MONDO:0010554	Abruzzo-Erickson syndrome
MONDO:0010553	Charcot-Marie-Tooth peroneal muscular atrophy and Friedreich ataxia, combined
MONDO:0010556	X-linked chondrodysplasia punctata
MONDO:0010555	X-linked chondrodysplasia punctata 1
MONDO:0022529	BK-virus nephropathy
MONDO:0009549	severe early-childhood-onset retinal dystrophy
MONDO:0009548	renal hypomagnesemia 5 with ocular involvement
MONDO:0009547	macrosomia-microphthalmia-cleft palate syndrome
MONDO:0010536	tubulin, beta
MONDO:0010535	Bazex-Dupre-Christol syndrome
MONDO:0009546	macrosomia adiposa congenita
MONDO:0010538	Mononen-Karnes-Senac syndrome
MONDO:0009545	macroepiphyseal dysplasia with osteoporosis, wrinkled skin, and aged appearance
MONDO:0010537	Borjeson-Forssman-Lehmann syndrome
MONDO:0009544	macrocephaly/megalencephaly syndrome, autosomal recessive
MONDO:0009543	prominent glabella-microcephaly-hypogenitalism syndrome
MONDO:0010539	X-linked mandibulofacial dysostosis
MONDO:0009542	lysine malabsorption syndrome
MONDO:0009541	lymphopenic hypergammaglobulinemia, antibody deficiency, autoimmune hemolytic anemia, and glomerulonephritis
MONDO:0009540	chronic mucocutaneous candidiasis due to lymphokine deficiency
MONDO:0010541	X-linked calvarial hyperostosis
MONDO:0010540	bullous dystrophy, macular type
MONDO:0010543	Barth syndrome
MONDO:0010542	dilated cardiomyopathy 3B
MONDO:0010545	Nance-Horan syndrome
MONDO:0010544	cataract 40
MONDO:0022518	autoimmune inner ear disease
MONDO:0022519	autoimmune myocarditis
MONDO:0022510	atlanto-axial fusion
MONDO:0022512	atrial septal defect coronary sinus
MONDO:0022513	atrophoderma of Pierini and Pasini
MONDO:0009559	mandibulofacial dysostosis with mental deficiency
MONDO:0010525	neural tube defects, X-linked
MONDO:0009558	Treacher Collins syndrome 3
MONDO:0009557	mandibuloacral dysplasia with type A lipodystrophy
MONDO:0010524	X-linked sideroblastic anemia with ataxia
MONDO:0009556	malonic aciduria
MONDO:0010527	microphthalmia-ankyloblepharon-intellectual disability syndrome
MONDO:0009555	malocclusion and short stature
MONDO:0010526	Fabry disease
MONDO:0010529	X-linked spinocerebellar ataxia type 3
MONDO:0009554	3MC syndrome 3
MONDO:0010528	anosmia
MONDO:0009553	Plasmodium falciparum blood infection level
MONDO:0009552	mal de Meleda
MONDO:0009551	magnesium, elevated red cell
MONDO:0009550	renal hypomagnesemia 3
MONDO:0010530	anus, imperforate
MONDO:0010532	infantile-onset X-linked spinal muscular atrophy
MONDO:0010531	contractures-ectodermal dysplasia-cleft lip/palate syndrome
MONDO:0010534	X-linked spinocerebellar ataxia type 4
MONDO:0010533	Arts syndrome
MONDO:0022504	arthrogryposis spinal muscular atrophy
MONDO:0022509	asternia
MONDO:0009609	methylcobalamin deficiency type cblG
MONDO:0009608	methionine malabsorption syndrome
MONDO:0009607	methionine adenosyltransferase deficiency
MONDO:0009606	methemoglobinemia due to deficiency of methemoglobin reductase
MONDO:0009605	methemoglobinemia type 4
MONDO:0009604	methemoglobin reductase deficiency
MONDO:0009603	3-hydroxyisobutyryl-CoA hydrolase deficiency
MONDO:0009602	metaphyseal modeling abnormality, skin lesions, and spastic paraplegia
MONDO:0009601	metaphyseal dysplasia without hypotrichosis
MONDO:0009600	metaphyseal dysplasia, anetoderma, and optic atrophy
MONDO:0010600	granulomatous disease, chronic, X-linked
MONDO:0009619	microcephaly-micromelia syndrome
MONDO:0009618	microcephaly-cardiomyopathy syndrome
MONDO:0009617	microcephaly 1, primary, autosomal recessive
MONDO:0009616	microcephalic primordial dwarfism, Toriello type
MONDO:0009615	methylmalonic acidemia due to methylmalonyl-CoA epimerase deficiency
MONDO:0009614	vitamin B12-responsive methylmalonic acidemia type cblB
MONDO:0009613	vitamin B12-responsive methylmalonic acidemia type cblA
MONDO:0009612	methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency
MONDO:0009611	3-methylglutaconic aciduria type 4
MONDO:0009610	3-methylglutaconic aciduria type 1
MONDO:0022462	anophthalmia esophageal atresia cryptorchidism
MONDO:0022463	anophthalmia megalocornea cardiopathy skeletal anomalies
MONDO:0022464	anophthalmia microcephaly hypogonadism
MONDO:0022465	anotia facial palsy cardiac defect
MONDO:0022468	antigen-peptide-transporter 2 deficiency
MONDO:0022469	aortic arches defect
MONDO:0009489	hereditary palmoplantar keratoderma, Gamborg-Nielsen type
MONDO:0009488	keratoconus posticus circumscriptus
MONDO:0009487	keratoconus and congenital hip dysplasia
MONDO:0009486	autosomal recessive Kenny-Caffey syndrome
MONDO:0022460	anophthalmia cleft lip palate hypothalamic disorder
MONDO:0009485	oculocerebrofacial syndrome, Kaufman type
MONDO:0022461	anophthalmia cleft palate micrognathia
MONDO:0010484	deafness, X-linked 6
MONDO:0009484	primary ciliary dyskinesia 1
MONDO:0010483	X-linked intellectual disability, Cantagrel type
MONDO:0009483	kapur-Toriello syndrome
MONDO:0009482	hypogonadotropic hypogonadism 3 with or without anosmia
MONDO:0010486	Olmsted syndrome, X-linked
MONDO:0010485	X-linked colobomatous microphthalmia-microcephaly-intellectual disability-short stature syndrome
MONDO:0009481	Jumping Frenchmen of Maine
MONDO:0009480	Joubert syndrome with oculorenal defect
MONDO:0010488	intellectual disability, X-linked 100
MONDO:0010487	intellectual disability, X-linked 99
MONDO:0010489	intellectual disability, X-linked 101
MONDO:0010480	anemia, nonspherocytic hemolytic, due to G6PD deficiency
MONDO:0010482	X-linked parkinsonism-spasticity syndrome
MONDO:0010481	angioedema
MONDO:0022453	angiomyomatous hamartoma
MONDO:0022454	angiosarcoma of the scalp
MONDO:0022456	ankle defects short stature
MONDO:0022457	ankyloblepharon filiforme imperforate anus
MONDO:0022458	annular constricting bands
MONDO:0010469	epsilon-trimethyllysine hydroxylase deficiency
MONDO:0009499	Krabbe disease
MONDO:0009498	lethal Kniest-like dysplasia
MONDO:0009497	Kifafa seizure disorder
MONDO:0009496	Kniest-like dysplasia with pursed lips and ectopia lentis
MONDO:0009495	Keutel syndrome
MONDO:0010473	X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome
MONDO:0010472	developmental and epileptic encephalopathy, 36
MONDO:0009494	Ketoadipicaciduria
MONDO:0010475	X-linked central congenital hypothyroidism with late-onset testicular enlargement
MONDO:0009493	Richards-Rundle syndrome
MONDO:0009492	succinyl-CoA:3-ketoacid CoA transferase deficiency
MONDO:0010474	linear skin defects with multiple congenital anomalies 2
MONDO:0009491	Haim-Munk syndrome
MONDO:0010477	blepharophimosis - intellectual disability syndrome, MKB type
MONDO:0009490	Papillon-Lefevre disease
MONDO:0010476	neurodegeneration with brain iron accumulation 5
MONDO:0010479	Charcot-Marie-Tooth disease X-linked dominant 6
MONDO:0010478	SLC35A2-CDG
MONDO:0022448	amyoplasia mandibulofacial dysostosis
MONDO:0010471	Cornelia de Lange syndrome 5
MONDO:0010470	Baratela-Scott syndrome
MONDO:0022444	amyloidosis bronchopulmonary
MONDO:0022446	amyloidosis nodular localized cutaneous
MONDO:0010459	amyotrophic lateral sclerosis type 15
MONDO:0010458	hypospadias 4, X-linked
MONDO:0009469	benign recurrent intrahepatic cholestasis type 1
MONDO:0009468	pseudotumor cerebri
MONDO:0009467	natal teeth-intestinal pseudoobstruction-patent ductus syndrome
MONDO:0009466	neuronal intestinal pseudoobstruction
MONDO:0009465	multiple intestinal atresia
MONDO:0009464	immunodeficiency with defective T-cell response to interleukin 1
MONDO:0009463	internal carotid arteries, hypoplasia of
MONDO:0010462	syndromic X-linked intellectual disability Chudley-Schwartz type
MONDO:0009462	inosine phosphorylase deficiency, immune defect due to
MONDO:0009461	male infertility due to large-headed multiflagellar polyploid spermatozoa
MONDO:0010461	syndromic X-linked intellectual disability Nascimento type
MONDO:0009460	indolylacroyl glycinuria with intellectual disability
MONDO:0010464	X-linked cerebral-cerebellar-coloboma syndrome syndrome
MONDO:0010463	X-linked dominant chondrodysplasia, Chassaing-Lacombe type
MONDO:0010466	multiple congenital anomalies-hypotonia-seizures syndrome 2
MONDO:0010465	Kabuki syndrome 2
MONDO:0010468	aneurysm, intracranial berry, 5
MONDO:0010467	Xq27.3q28 duplication syndrome
MONDO:0010460	syndromic X-linked intellectual disability 17
MONDO:0022430	persistent fetal circulation syndrome
MONDO:0022432	alves Castelo dos Santos syndrome
MONDO:0022434	amelia cleft lip palate hydrocephalus iris coloboma
MONDO:0022435	Mauriac syndrome
MONDO:0010448	moyamoya angiopathy-short stature-facial dysmorphism-hypergonadotropic hypogonadism syndrome
MONDO:0010447	intellectual disability, X-linked 19
MONDO:0009479	Johanson-Blizzard syndrome
MONDO:0009478	combined immunodeficiency due to DOCK8 deficiency
MONDO:0010449	autism, susceptibility to, X-linked 5
MONDO:0009477	Stromme syndrome
MONDO:0009476	atresia of small intestine
MONDO:0009475	isovaleric acidemia
MONDO:0009474	isovaleric acid, inability to smell
MONDO:0010451	intellectual disability, X-linked 41
MONDO:0009473	isotretinoin-like syndrome
MONDO:0009472	acetylation, slow
MONDO:0010450	intellectual disability, X-linked 89
MONDO:0009471	intrinsic factor and r binder, combined congenital deficiency of
MONDO:0010453	intellectual disability, X-linked 92
MONDO:0009470	Baraitser-Winter syndrome 1
MONDO:0010452	intellectual disability, X-linked 90
MONDO:0010455	X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection and neoplasia
MONDO:0010454	intellectual disability, XMEN-linked 88
MONDO:0010457	Ogden syndrome
MONDO:0010456	renal cell carcinoma, Xp11-associated
MONDO:0022428	aluminosis
MONDO:0022495	arthritis short stature deafness
MONDO:0022496	arthrogryposis IUGR thoracic dystrophy
MONDO:0022481	APO A-i deficiency
MONDO:0022482	apolipoprotein C 2i deficiency
MONDO:0022470	aortic dissection lentiginosis
MONDO:0022471	childhood aortic valve stenosis
MONDO:0010495	trichothiodystrophy 5, nonphotosensitive
MONDO:0010494	linear skin defects with multiple congenital anomalies 3
MONDO:0010497	intellectual disability, X-linked 102
MONDO:0010496	X-linked intellectual disability-short stature-overweight syndrome
MONDO:0010499	Ritscher-Schinzel syndrome 2
MONDO:0010498	MEND syndrome
MONDO:0010491	X-linked acrogigantism due to Xq26 microduplication
MONDO:0010490	SSR4-CDG
MONDO:0010493	Diamond-Blackfan anemia 14 with mandibulofacial dysostosis
MONDO:0010492	pituitary adenoma, growth hormone-secreting, 2
MONDO:0009409	hypervitaminosis a, susceptibility to
MONDO:0009408	hyperuricemia, infantile, with abnormal behavior and normal hypoxanthine guanine phosphoribosyltransferase
MONDO:0009407	hypertrophic neuropathy and cataract
MONDO:0009406	hypertrichotic osteochondrodysplasia Cantu type
MONDO:0009405	cervical hypertrichosis-peripheral neuropathy syndrome
MONDO:0009404	hypertelorism, microtia, facial clefting syndrome
MONDO:0009403	hypertelorism and tetralogy of fallot
MONDO:0009402	acrofrontofacionasal dysostosis 2
MONDO:0009401	hyperprolinemia type 2
MONDO:0009400	hyperprolinemia type 1
MONDO:0010400	X-linked scapuloperoneal muscular dystrophy
MONDO:0010402	syndromic X-linked intellectual disability 94
MONDO:0010401	X-linked myopathy with postural muscle atrophy
MONDO:0009419	Woodhouse-Sakati syndrome
MONDO:0009418	hypogonadism with low-grade mental deficiency and microcephaly
MONDO:0009417	hypergonadotropic hypogonadism-cataract syndrome
MONDO:0009416	hypoinsulinemic hypoglycemia and body hemihypertrophy
MONDO:0009415	hypoglycemia, leucine-induced
MONDO:0009414	glycogen storage disease due to hepatic glycogen synthase deficiency
MONDO:0009413	immunodeficiency, common variable, 2
MONDO:0009412	scurvy
MONDO:0009411	autoimmune polyendocrine syndrome type 1
MONDO:0009410	Addison disease
MONDO:0022423	alpha-2 deficient collagen disease
MONDO:0022424	alpha-mannosidosis type 1
MONDO:0009449	ciliary dyskinesia with defective radial spokes
MONDO:0022425	alpha-thalassemia-abnormal morphogenesis
MONDO:0009448	iminoglycinuria
MONDO:0010437	severe X-linked mitochondrial encephalomyopathy
MONDO:0009447	ichthyosis, split hairs, and amino aciduria
MONDO:0010436	chromosome Xq28 duplication syndrome
MONDO:0009446	ichthyosis-intellectual disability-dwarfism-renal impairment syndrome
MONDO:0010439	cardiomyopathy, fatal fetal, due to myocardial calcification
MONDO:0010438	paroxysmal nocturnal hemoglobinuria 1
MONDO:0009445	ichthyosis-hepatosplenomegaly-cerebellar degeneration syndrome
MONDO:0009444	ichthyosis-alopecia-eclabion-ectropion-intellectual disability syndrome
MONDO:0009443	autosomal recessive congenital ichthyosis 4B
MONDO:0009442	ichthyosis congenita with biliary atresia
MONDO:0009441	autosomal recessive congenital ichthyosis 1
MONDO:0010440	autism, susceptibility to, X-linked 4
MONDO:0009440	ichthyosiform erythroderma, corneal involvement, and deafness
MONDO:0010442	46,XX sex reversal 3
MONDO:0010441	CK syndrome
MONDO:0010444	X-linked dyserythropoetic anemia with abnormal platelets and neutropenia
MONDO:0010443	macular degeneration, X-linked atrophic
MONDO:0010446	X-linked cone dysfunction syndrome with myopia
MONDO:0010445	McLeod syndrome
MONDO:0022417	alopecia congenita keratosis palmoplantaris
MONDO:0022418	alopecia immunodeficiency
MONDO:0022410	retinal ciliopathy
MONDO:0022412	albinism immunodeficiency
MONDO:0022413	Albright-like syndrome
MONDO:0022414	allain-babin-demarquez syndrome
MONDO:0010426	X-linked endothelial corneal dystrophy
MONDO:0009459	channelopathy-associated congenital insensitivity to pain, autosomal recessive
MONDO:0009458	Schimke immuno-osseous dysplasia
MONDO:0010425	Lisch epithelial corneal dystrophy
MONDO:0010428	chromosome Xp11.23-p11.22 duplication syndrome
MONDO:0009457	immunoglobulin d level in plasma, low
MONDO:0010427	syndromic X-linked intellectual disability Raymond type
MONDO:0009456	Immunoerythromyeloid hypoplasia
MONDO:0009455	immunodeficiency, partial combined, with absence of HLA Determinants and beta-2-microglobulin from lymphocytes
MONDO:0009454	immunodeficiency-centromeric instability-facial anomalies syndrome 1
MONDO:0010429	intellectual disability, X-linked 96
MONDO:0009453	immune deficiency disease
MONDO:0009452	Vici syndrome
MONDO:0009451	Nezelof syndrome
MONDO:0009450	ciliary dyskinesia with excessively long cilia
MONDO:0010431	Joubert syndrome 10
MONDO:0010430	intellectual disability, X-linked 97
MONDO:0010433	systemic lupus erythematosus, susceptibility to, 15
MONDO:0010432	thrombophilia, X-linked, due to factor 9 defect
MONDO:0010435	nystagmus 6, congenital, X-linked
MONDO:0010434	synovial sarcoma
MONDO:0022404	retinal ciliopathy due to mutation in usher gene
MONDO:0022405	retinal ciliopathy due to mutation in nephronophthisis gene
MONDO:0022406	aksu von stockhausen syndrome
MONDO:0022407	retinal ciliopathy due to mutation in bardet-biedl gene
MONDO:0022409	nephropathy-associated ciliopathy
MONDO:0022400	retinal ciliopathy due to mutation in the rpgrip gene
MONDO:0009429	hypophosphatemia, renal, with intracerebral calcifications
MONDO:0022401	agyria pachygyria polymicrogyria
MONDO:0009428	childhood hypophosphatasia
MONDO:0022402	agyria-pachygyria type 1
MONDO:0022403	Ahumada Del Castillo syndrome
MONDO:0009427	infantile hypophosphatasia
MONDO:0009426	hypoparathyroidism-retardation-dysmorphism syndrome
MONDO:0010415	myopathy, reducing body, X-linked, childhood-onset
MONDO:0009425	hypomandibular faciocranial dysostosis
MONDO:0010414	myopathy, reducing body, X-linked, early-onset, severe
MONDO:0009424	Bartter disease type 2
MONDO:0010417	syndromic X-linked intellectual disability Najm type
MONDO:0009423	hypokalemic alkalosis, familial, with specific renal tubulopathy
MONDO:0010416	deafness, cataract, retinitis pigmentosa, and sperm abnormalities
MONDO:0010419	X-linked sideroblastic anemia
MONDO:0009422	hypohidrosis with abnormal palmar dermal Ridges
MONDO:0010418	hereditary spastic paraplegia 34
MONDO:0009421	hypogonadism, male
MONDO:0009420	primary hypergonadotropic hypogonadism-partial alopecia syndrome
MONDO:0010420	X-linked erythropoietic protoporphyria
MONDO:0010422	Alzheimer disease 16
MONDO:0010421	Bruton-type agammaglobulinemia
MONDO:0010424	surfactant metabolism dysfunction, pulmonary, 4
MONDO:0010423	hypospadias 2, X-linked
MONDO:0009439	autosomal recessive congenital ichthyosis 2
MONDO:0009438	hypouricemia, hypercalcinuria, and decreased bone density
MONDO:0010404	X-linked non progressive cerebellar ataxia
MONDO:0009437	Bamforth-Lazarus syndrome
MONDO:0010403	albinism-deafness syndrome
MONDO:0009436	congenital hypothalamic hamartoma syndrome
MONDO:0009435	hypospadias-intellectual disability, Goldblatt type syndrome
MONDO:0010406	chromosome Xp11.22 duplication syndrome
MONDO:0009434	hypoproteinemia, hypercatabolic
MONDO:0010405	prostate cancer, hereditary, X-linked 2
MONDO:0009433	hypoplastic left heart syndrome 1
MONDO:0010408	syndactyly-telecanthus-anogenital and renal malformations syndrome
MONDO:0010407	intellectual disability, X-linked syndromic, Turner type
MONDO:0009432	hypopituitarism, congenital, with central diabetes insipidus
MONDO:0009431	hereditary hypophosphatemic rickets with hypercalciuria
MONDO:0010409	syndromic X-linked intellectual disability Shrimpton type
MONDO:0009430	hypophosphatemic rickets, autosomal recessive, 1
MONDO:0010411	pyloric stenosis, infantile hypertrophic, 4
MONDO:0010410	alopecia, androgenetic, 2
MONDO:0010413	intellectual disability, X-linked 95
MONDO:0010412	X-linked intellectual disability-craniofacioskeletal syndrome
MONDO:0010359	Dent disease type 2
MONDO:0009369	non-immune hydrops fetalis
MONDO:0009368	urofacial syndrome type 1
MONDO:0009367	McKusick-Kaufman syndrome
MONDO:0009366	normal pressure hydrocephalus
MONDO:0009365	hydrolethalus syndrome 1
MONDO:0009364	muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A1
MONDO:0010363	intellectual disability, X-linked 91
MONDO:0009363	hydrocephaly-tall stature-joint laxity syndrome
MONDO:0010362	glycogen storage disease IXd
MONDO:0009362	growth delay-hydrocephaly-lung hypoplasia syndrome
MONDO:0010365	myopathy, congenital, with fiber-type disproportion, X-linked
MONDO:0009361	autosomal recessive hydrocephalus due to congenital stenosis of aqueduct of Sylvius
MONDO:0010364	X-linked intellectual disability-retinitis pigmentosa syndrome
MONDO:0009360	hydrocephalus, nonsyndromic, autosomal recessive 1
MONDO:0010367	SHOX-related short stature
MONDO:0010366	FG syndrome 5
MONDO:0010369	nystagmus 5, congenital, X-linked
MONDO:0010368	immunodeficiency without anhidrotic ectodermal dysplasia
MONDO:0022338	ALK+ histiocytosis
MONDO:0036990	benign Leydig cell tumor
MONDO:0010361	intellectual disability, X-linked 30
MONDO:0010360	parkinson disease 12
MONDO:0022330	4-hydroxyphenylacetic aciduria
MONDO:0022333	5-nucleotidase syndrome
MONDO:0024996	Usher syndrome, type 2b
MONDO:0022337	AIDS dysmorphic syndrome
MONDO:0010349	ovarian dysgenesis 2
MONDO:0010348	dyslexia, susceptibility to, 9
MONDO:0009379	Rotor syndrome
MONDO:0009378	hyper-beta-alaninemia
MONDO:0009377	hyperammonemia due to N-acetylglutamate synthase deficiency
MONDO:0009376	carbamoyl phosphate synthetase I deficiency disease
MONDO:0009375	hymen, imperforate
MONDO:0024990	swine disease
MONDO:0009374	hydroxyprolinemia
MONDO:0010352	intellectual disability, X-linked 82
MONDO:0009373	seizures-intellectual disability due to hydroxylysinuria syndrome
MONDO:0010351	Fanconi anemia complementation group B
MONDO:0010354	Allan-Herndon-Dudley syndrome
MONDO:0009372	encephalopathy due to hydroxykynureninuria
MONDO:0010353	deafness-intellectual disability, Martin-Probst type syndrome
MONDO:0009371	3-hydroxyisobutyric aciduria
MONDO:0009370	L-2-hydroxyglutaric aciduria
MONDO:0010356	nephrogenic syndrome of inappropriate antidiuresis
MONDO:0010355	syndromic X-linked intellectual disability Claes-Jensen type
MONDO:0010358	hypophosphatemic rickets, X-linked recessive
MONDO:0010357	MRX78
MONDO:0010350	premature ovarian failure 2A
MONDO:0024982	salmonella infections, animal
MONDO:0024981	rodent disease
MONDO:0022321	2-methylacetoacetyl CoA thiolase deficiency
MONDO:0022323	2-hydroxyethyl methacrylate sensitization
MONDO:0024985	sheep disease
MONDO:0024988	sex cord-stromal benign neoplasm
MONDO:0010338	X-linked distal spinal muscular atrophy type 3
MONDO:0009349	holoprosencephaly 1
MONDO:0010337	X-linked intellectual disability-cerebellar hypoplasia syndrome
MONDO:0009348	classic Hodgkin lymphoma
MONDO:0009347	familial lipochrome histiocytosis
MONDO:0012999	guanidinoacetate methyltransferase deficiency
MONDO:0010339	X-linked epilepsy-learning disabilities-behavior disorders syndrome
MONDO:0009346	histidinuria due to a renal tubular defect
MONDO:0009345	histidinemia
MONDO:0009344	Hirschsprung disease-nail hypoplasia-dysmorphism syndrome
MONDO:0009343	Hirschsprung disease with ulnar polydactyly, polysyndactyly of big toes, and ventricular septal defect
MONDO:0009342	Hirschsprung disease-deafness-polydactyly syndrome
MONDO:0009341	Mowat-Wilson syndrome
MONDO:0010341	autism, susceptibility to, X-linked 2
MONDO:0009340	non-spherocytic hemolytic anemia due to hexokinase deficiency
MONDO:0010340	Asperger syndrome, X-linked, susceptibility to, 1
MONDO:0010343	Asperger syndrome, X-linked, susceptibility to, 2
MONDO:0010342	autism, susceptibility to, X-linked 3
MONDO:0010345	ocular albinism
MONDO:0010344	intellectual disability, X-linked 45
MONDO:0010347	intellectual disability, X-linked 84
MONDO:0010346	MRX52
MONDO:0022316	hair defect with photosensitivity and intellectual disability syndrome
MONDO:0024971	parturient paresis
MONDO:0024973	pneumonia, atypical interstitial, of cattle
MONDO:0022311	cote katsantoni syndrome
MONDO:0022314	Hernandez Aguirre-Negrete syndrome
MONDO:0010327	HSD10 mitochondrial disease
MONDO:0010326	intellectual disability, X-linked 46
MONDO:0009359	multinucleated neurons-anhydramnios-renal dysplasia-cerebellar hypoplasia-hydranencephaly syndrome
MONDO:0012988	hypogonadotropic hypogonadism 6 with or without anosmia
MONDO:0010329	intellectual disability, X-linked 77
MONDO:0009358	Hutterite cerebroosteonephrodysplasia syndrome
MONDO:0010328	alpha-thalassemia-myelodysplastic syndrome
MONDO:0012989	microcephaly 7, primary, autosomal recessive
MONDO:0009357	humeroradial synostosis with craniofacial anomalies
MONDO:0009356	autosomal recessive humeroradial synostosis
MONDO:0009355	Hooft disease
MONDO:0009354	methylcobalamin deficiency type cblE
MONDO:0009353	homocystinuria due to methylene tetrahydrofolate reductase deficiency
MONDO:0010330	primary ciliary dyskinesia-retinitis pigmentosa syndrome
MONDO:0009352	classic homocystinuria
MONDO:0012993	dyschromatosis universalis hereditaria 2
MONDO:0012994	dopa-responsive dystonia due to sepiapterin reductase deficiency
MONDO:0009351	homocarnosinosis
MONDO:0010332	X-linked intellectual disability-cubitus valgus-dysmorphism syndrome
MONDO:0012991	Kahrizi syndrome
MONDO:0009350	Holzgreve-Wagner-Rehder syndrome
MONDO:0012992	pancreatic insufficiency-anemia-hyperostosis syndrome
MONDO:0010331	coronary heart disease, susceptibility to, 3
MONDO:0012997	cholestasis-pigmentary retinopathy-cleft palate syndrome
MONDO:0010334	severe motor and intellectual disabilities-sensorineural deafness-dystonia syndrome
MONDO:0010333	corpus callosum agenesis-intellectual disability-coloboma-micrognathia syndrome
MONDO:0012998	faciocardiomelic syndrome
MONDO:0010336	orofaciodigital syndrome VIII
MONDO:0012995	myopia 15, autosomal dominant
MONDO:0010335	X-linked cone-rod dystrophy 3
MONDO:0012996	AGAT deficiency
MONDO:0024969	parasitic disease, non-human animal
MONDO:0022308	corticobasal degeneration disorder
MONDO:0012990	Leber congenital amaurosis 13
MONDO:8000005	fungal discitis
MONDO:8000004	salmonella discitis
MONDO:0022380	acute lymphoblastic leukemia congenital sporadic aniridia
MONDO:8000001	staphylococcus discitis
MONDO:8000000	infectious discitis
MONDO:8000003	streptococcus pneumoniae discitis
MONDO:8000002	escherichia coli discitis
MONDO:0010396	developmental and epileptic encephalopathy, 2
MONDO:0010395	phosphoribosylpyrophosphate synthetase superactivity
MONDO:0010398	syndromic X-linked intellectual disability 14
MONDO:0010397	severe neonatal-onset encephalopathy with microcephaly
MONDO:0010399	chromosome Xp21 deletion syndrome
MONDO:0010390	ocular albinism with late-onset sensorineural deafness
MONDO:0010392	glycogen storage disease due to phosphoglycerate kinase 1 deficiency
MONDO:0010391	angioma serpiginosum, X-linked
MONDO:0010394	leukoencephalopathy-metaphyseal chondrodysplasia syndrome
MONDO:0010393	intellectual disability, X-linked 93
MONDO:0009389	hyperlysinemia due to defect in lysine transport into mitochondria
MONDO:0009388	hyperlysinemia
MONDO:0009387	familial lipoprotein lipase deficiency
MONDO:0009386	hyperlexia
MONDO:0010385	X-linked lymphoproliferative disease due to XIAP deficiency
MONDO:0009385	hyperleucine-Isoleucinemia
MONDO:0010384	hypospadias 1, X-linked
MONDO:0009384	Leydig cell hypoplasia, type 1
MONDO:0009383	transient familial neonatal hyperbilirubinemia
MONDO:0010387	invasive pneumococcal disease, recurrent isolated, 2
MONDO:0009382	hyperbilirubinemia, shunt, primary
MONDO:0010386	immunodeficiency 33
MONDO:0009381	hyperbilirubinemia, conjugated, type 3
MONDO:0010389	X-linked mendelian susceptibility to mycobacterial diseases due to CYBB deficiency
MONDO:0010388	rolandic epilepsy, intellectual disability, and speech dyspraxia, X-linked
MONDO:0009380	Dubin-Johnson syndrome
MONDO:0036976	benign epithelial neoplasm
MONDO:0010381	Tn polyagglutination syndrome
MONDO:0010380	cataract, ataxia, short stature, and intellectual disability
MONDO:0010383	fragile X syndrome
MONDO:0010382	fragile X-associated tremor/ataxia syndrome
MONDO:0022357	congenital acardia
MONDO:0009399	hyperphosphatemia, polyuria, and seizures
MONDO:0009398	hyperphosphatasia with intellectual disability syndrome 1
MONDO:0009397	neonatal severe primary hyperparathyroidism
MONDO:0010374	retinitis pigmentosa 34
MONDO:0009396	hyperparathyroidism, neonatal self-limited primary, with hypercalciuria
MONDO:0009395	hyperostosis corticalis generalisata
MONDO:0010373	premature ovarian failure 2B
MONDO:0009394	juvenile Paget disease
MONDO:0010376	Brooks-Wisniewski-brown syndrome
MONDO:0010375	developmental and epileptic encephalopathy, 8
MONDO:0009393	ornithine translocase deficiency
MONDO:0010378	X-linked hereditary sensory and autonomic neuropathy with deafness
MONDO:0009392	hyperopia, high
MONDO:0009391	hypermetabolism due to defect in mitochondria
MONDO:0010377	myopia 13, X-linked
MONDO:0009390	hyperlysinuria with hyperammonemia
MONDO:0010379	Brunner syndrome
MONDO:0022349	congenital absence of septum pellucidum
MONDO:0010370	Cornelia de Lange syndrome 2
MONDO:0010372	Clark-Baraitser syndrome
MONDO:0010371	Aland island eye disease
MONDO:0000953	cancer of short bone of lower limb
MONDO:0000952	cancer of long bone of lower limb
MONDO:0000951	thymus lymphoma
MONDO:0000950	asthenopia
MONDO:0012935	leukemia, chronic lymphocytic, susceptibility to, 4
MONDO:0012936	leukemia, chronic lymphocytic, susceptibility to, 5
MONDO:0012933	breast-ovarian cancer, familial, susceptibility to, 2
MONDO:0012934	leukemia, chronic lymphocytic, susceptibility to, 3
MONDO:0012939	Diamond-Blackfan anemia 8
MONDO:0012937	Diamond-Blackfan anemia 6
MONDO:0012938	Diamond-Blackfan anemia 7
MONDO:0012942	lung cancer susceptibility 3
MONDO:0012943	retinitis pigmentosa 46
MONDO:0012940	inflammatory bowel disease 24
MONDO:0012941	inflammatory bowel disease 25
MONDO:0000946	psychologic vaginismus
MONDO:0024913	cattle disease
MONDO:0000945	venous insufficiency
MONDO:0024912	cat disease
MONDO:0000944	cerebral artery occlusion
MONDO:0000943	acute hydrops keratoconus
MONDO:0000949	conjunctival degeneration
MONDO:0000948	xerophthalmia
MONDO:0024919	dog disease
MONDO:0000947	psychosexual disorder
MONDO:0000960	diabetic peripheral angiopathy
MONDO:0000964	skin lipoma
MONDO:0000963	esophageal lipoma
MONDO:0000962	spindle cell lipoma
MONDO:0000961	endobronchial lipoma
MONDO:0012924	Diamond-Blackfan anemia 4
MONDO:0012925	Diamond-Blackfan anemia 5
MONDO:0036915	benign ovarian mucinous tumor
MONDO:0012922	pyloric stenosis, infantile hypertrophic, 5
MONDO:0012923	congenital generalized lipodystrophy type 3
MONDO:0012928	hereditary spastic paraplegia 42
MONDO:0012929	Compton-North congenital myopathy
MONDO:0036918	punctate acrokeratoderma freckle-like pigmentation
MONDO:0012926	amelogenesis imperfecta hypomaturation type 2A2
MONDO:0012927	chromosome 1q41-q42 deletion syndrome
MONDO:0012931	focal segmental glomerulosclerosis 4, susceptibility to
MONDO:0012932	myopia 16, autosomal dominant
MONDO:0012930	autosomal recessive severe congenital neutropenia due to G6PC3 deficiency
MONDO:0000957	lacrimal passage granuloma
MONDO:0000956	small intestine cancer
MONDO:0000955	ileum cancer
MONDO:0000954	Meckel diverticulum cancer
MONDO:0024905	bird disease
MONDO:0000959	malignant hypertensive renal disease
MONDO:0000958	neuroretinitis
MONDO:0012919	type 1 diabetes mellitus 20
MONDO:0000931	endometrial disease
MONDO:0000930	nodular malignant melanoma
MONDO:0012913	Wilms tumor, aniridia, genitourinary anomalies, intellectual disability, and obesity syndrome
MONDO:0012914	chromosome 1q21.1 deletion syndrome
MONDO:0012911	pseudohypoparathyroidism type 1C
MONDO:0012912	pseudopseudohypoparathyroidism
MONDO:0012917	specific language impairment 4
MONDO:0012918	primary ciliary dyskinesia 10
MONDO:0012915	chromosome 1q21.1 duplication syndrome
MONDO:0012916	chromosome 2p16.1-p15 deletion syndrome
MONDO:0000929	balloon cell malignant melanoma
MONDO:0012920	type 1 diabetes mellitus 21
MONDO:0012921	type 1 diabetes mellitus 22
MONDO:0000924	compensatory emphysema
MONDO:0000923	interstitial emphysema
MONDO:0000922	pelvic inflammatory disease
MONDO:0000921	ampulla of vater neoplasm
MONDO:0000928	eyelid melanoma
MONDO:0000927	asymptomatic neurosyphilis
MONDO:0000926	eye accommodation disease
MONDO:0000925	hyperlucent lung
MONDO:0012908	complement component 6 deficiency
MONDO:0012909	skeletal defects, genital hypoplasia, and intellectual disability
MONDO:0000942	corneal disease
MONDO:0000941	eyelid degenerative disease
MONDO:0000940	trypanosomiasis
MONDO:0012902	autosomal dominant nonsyndromic deafness 27
MONDO:0012903	autosomal recessive nonsyndromic deafness 45
MONDO:0012900	cardiomyopathy, familial restrictive, 3
MONDO:0012901	inherited prekallikrein deficiency
MONDO:0012906	primary ciliary dyskinesia 9
MONDO:0012907	blindness - scoliosis - arachnodactyly syndrome
MONDO:0012904	epilepsy, progressive myoclonic, 1B
MONDO:0012905	hypomyelinating leukodystrophy 6
MONDO:0012910	age-related hearing impairment 1
MONDO:0000935	larynx squamous papilloma
MONDO:0000934	laryngeal leiomyoma
MONDO:0000933	subglottis neoplasm
MONDO:0000932	skin amelanotic melanoma
MONDO:0000939	intracranial abscess
MONDO:0000938	gastric leiomyoma
MONDO:0000937	syphilitic encephalitis
MONDO:0000936	syphilitic meningitis
MONDO:0000993	prostate squamous cell carcinoma
MONDO:0000992	heart conduction disease
MONDO:0000991	left bundle branch block
MONDO:0000990	acute subendocardial myocardial infarction
MONDO:0000997	monocular esotropia
MONDO:0000996	prostate lymphoma
MONDO:0009329	pulmonary venoocclusive disease 2
MONDO:0000995	familial periodic paralysis
MONDO:0009328	hemangiomatosis, cutaneous, with associated features
MONDO:0024965	muscular dystrophy, non-human animal
MONDO:0000994	malignant prostate phyllodes tumor
MONDO:0012979	primary ciliary dyskinesia 12
MONDO:0009327	heart, malformation of
MONDO:0010316	FG syndrome 3
MONDO:0010315	T-B+ severe combined immunodeficiency due to gamma chain deficiency
MONDO:0009326	congenital heart block
MONDO:0009325	deafness-enamel hypoplasia-nail defects syndrome
MONDO:0010318	FG syndrome 4
MONDO:0012977	autosomal recessive nonsyndromic deafness 1B
MONDO:0009324	Hartnup disease
MONDO:0010317	intellectual disability, X-linked, with or without seizures, arx-related
MONDO:0012978	primary ciliary dyskinesia 11
MONDO:0009323	Halothane hepatitis
MONDO:0009322	halo nevi
MONDO:0010319	syndromic X-linked intellectual disability Hedera type
MONDO:0009321	hallux varus-preaxial polysyndactyly syndrome
MONDO:0009320	Hall-Riggs syndrome
MONDO:0012982	episodic ataxia type 6
MONDO:0012983	cone-rod dystrophy 12
MONDO:0012980	endocrine-cerebro-osteodysplasia syndrome
MONDO:0010321	autism, susceptibility to, X-linked 1
MONDO:0012981	hereditary spherocytosis type 4
MONDO:0010320	retinitis pigmentosa 23
MONDO:0010323	Atkin-Flaitz syndrome
MONDO:0012986	bilateral parasagittal parieto-occipital polymicrogyria
MONDO:0010322	intellectual disability, X-linked 2
MONDO:0012987	agammaglobulinemia 6, autosomal recessive
MONDO:0012984	PHARC syndrome
MONDO:0010325	X-linked intellectual disability, Stocco dos Santos type
MONDO:0010324	intellectual disability, X-linked 81
MONDO:0012985	hereditary spherocytosis type 5
MONDO:0000989	mumps infectious disease
MONDO:0000988	discharging ear
MONDO:0000987	cholesterolosis of gallbladder
MONDO:0024950	horse disease
MONDO:0024953	lameness, non-human animal
MONDO:0009339	congenital bile acid synthesis defect 2
MONDO:0024954	larva migrans, visceral
MONDO:0009338	hepatic veno-occlusive disease-immunodeficiency syndrome
MONDO:0012968	Usher syndrome type 1H
MONDO:0010305	creatine transporter deficiency
MONDO:0012969	microvascular complications of diabetes, susceptibility to, 5
MONDO:0009337	Hennekam lymphangiectasia-lymphedema syndrome 1
MONDO:0010304	Graves disease, susceptibility to, X-linked 1
MONDO:0012966	microvascular complications of diabetes, susceptibility to, 4
MONDO:0009336	hemosiderosis, pulmonary, with deficiency of gamma-a globulin
MONDO:0010307	intellectual disability, X-linked 73
MONDO:0010306	X-linked intellectual disability, Cabezas type
MONDO:0012967	hemolytic anemia due to adenylate kinase deficiency
MONDO:0009335	hemolytic uremic syndrome, atypical, susceptibility to, 1
MONDO:0010309	intellectual disability, X-linked 42
MONDO:0009334	hemolytic anemia with thermal sensitivity of red cells
MONDO:0009333	mullerian derivatives-lymphangiectasia-polydactyly syndrome
MONDO:0010308	thrombocytopenia, X-linked, with or without dyserythropoietic anemia
MONDO:0009332	congenital hematological disorder
MONDO:0009331	isolated hemihyperplasia
MONDO:0009330	hemangiopericytoma, malignant
MONDO:0012971	microvascular complications of diabetes, susceptibility to, 7
MONDO:0012972	febrile seizures, familial, 10
MONDO:0010310	osteopathia striata with cranial sclerosis
MONDO:0012970	microvascular complications of diabetes, susceptibility to, 6
MONDO:0012975	autosomal dominant nonsyndromic deafness 3B
MONDO:0010312	radial ray deficiency, X-linked
MONDO:0010311	Becker muscular dystrophy
MONDO:0012976	autosomal dominant nonsyndromic deafness 2B
MONDO:0010314	polymicrogyria, bilateral perisylvian, X-linked
MONDO:0012973	inflammatory bowel disease 26
MONDO:0012974	autosomal dominant nonsyndromic deafness 59
MONDO:0010313	intellectual disability, X-linked 63
MONDO:0024945	hepatitis, non-human animal
MONDO:0000999	pneumoconiosis
MONDO:0000998	parotid disease
MONDO:0000971	chest wall lipoma
MONDO:0000970	breast lipoma
MONDO:0000975	lipoma of spermatic cord
MONDO:0009309	granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 1
MONDO:0000974	axillary lipoma
MONDO:0009308	granulomatous disease, chronic, autosomal recessive, cytochrome b-negative
MONDO:0009307	granulomatous disease with defect in neutrophil chemotaxis
MONDO:0000973	external ear lipoma
MONDO:0000972	gallbladder lipoma
MONDO:0009306	combined immunodeficiency with skin granulomas
MONDO:0009305	granulocytopenia with immunoglobulin abnormality
MONDO:0012957	multiple sclerosis, susceptibility to, 3
MONDO:0012958	multiple sclerosis, susceptibility to, 4
MONDO:0009304	Gorlin-Chaudhry-Moss syndrome
MONDO:0009303	anti-glomerular basement membrane disease
MONDO:0012955	lung cancer susceptibility 4
MONDO:0009302	XY type gonadal dysgenesis-associated anomalies syndrome
MONDO:0012956	multiple sclerosis, susceptibility to, 2
MONDO:0009301	46,XY sex reversal 7
MONDO:0009300	Perrault syndrome 1
MONDO:0012959	psoriasis 11, susceptibility to
MONDO:0012960	intellectual disability, autosomal dominant 5
MONDO:0012961	type 1 diabetes mellitus 23
MONDO:0012964	chromosome 15q26-qter deletion syndrome
MONDO:0010301	thrombocythemia, X-linked
MONDO:0012965	seizures, benign familial infantile, 4
MONDO:0010300	intellectual disability, X-linked 53
MONDO:0012962	microvascular complications of diabetes, susceptibility to, 2
MONDO:0010303	colobomatous microphthalmia
MONDO:0012963	microvascular complications of diabetes, susceptibility to, 3
MONDO:0010302	Ito hypomelanosis
MONDO:0024935	foot rot
MONDO:0000968	kidney lipoma
MONDO:0000967	conventional lipoma
MONDO:0024934	fish disease
MONDO:0000966	pleomorphic lipoma
MONDO:0000965	liver lipoma
MONDO:0000969	pleural lipoma
MONDO:0000982	Brown's tendon sheath syndrome
MONDO:0000981	Histoplasma pericarditis
MONDO:0000980	aortic atherosclerosis
MONDO:0000986	pleurisy
MONDO:0009319	pantothenate kinase-associated neurodegeneration
MONDO:0000985	ehrlichiosis
MONDO:0009318	Hallermann-Streiff syndrome
MONDO:0000984	thalassemia
MONDO:0000983	exhibitionism
MONDO:0009317	nonphotosensitive trichothiodystrophy
MONDO:0012946	intellectual disability, autosomal dominant 3
MONDO:0009316	hair defect-photosensitivity-intellectual disability syndrome
MONDO:0009315	congenital factor XII deficiency
MONDO:0012947	intellectual disability, autosomal dominant 4
MONDO:0009314	GTP-cyclohydrolase I deficiency
MONDO:0012944	chromosome 17P13.3, telomeric, duplication syndrome
MONDO:0012945	amyotrophic lateral sclerosis type 11
MONDO:0009313	Grubben-de Cock-Borghgraef syndrome
MONDO:0009312	lipodystrophy due to peptidic growth factors deficiency
MONDO:0009311	grouped pigmentation of the retina
MONDO:0009310	granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
MONDO:0012948	chromosome 6pter-p24 deletion syndrome
MONDO:0012949	aneurysm, intracranial berry, 9
MONDO:0012950	aneurysm, intracranial berry, 10
MONDO:0012953	colorectal cancer, susceptibility to, 10
MONDO:0012954	colorectal cancer, susceptibility to, 11
MONDO:0012951	colorectal cancer, susceptibility to, 8
MONDO:0012952	colorectal cancer, susceptibility to, 9
MONDO:0000979	pinta disease
MONDO:0000978	extrahepatic bile duct lipoma
MONDO:0000977	chondroid lipoma
MONDO:0000976	paratesticular lipoma
MONDO:0022397	retinal ciliopathy due to mutation in the retinitis pigmentosa-1 gene
MONDO:0022398	aglossia and situs inversus
MONDO:0022399	retinal ciliopathy due to mutation in the RPGR gene
MONDO:0022394	cervical intraepithelial neoplasia
MONDO:0022220	Parinaud syndrome
MONDO:0024883	metastatic neoplasm
MONDO:0024882	secondary neoplasm
MONDO:0024885	malignant ovarian serous tumor
MONDO:0024884	metastatic carcinoma in the bone
MONDO:0024886	serous adenofibroma
MONDO:0024889	benign mesonephroma
MONDO:0024888	mesonephric neoplasm
MONDO:0010239	lissencephaly type 1 due to doublecortin gene mutation
MONDO:0009249	hereditary fructose intolerance
MONDO:0010238	deafness, X-linked 4
MONDO:0009248	fructose and galactose intolerance
MONDO:0009247	frontofacionasal dysplasia
MONDO:0009246	Friedreich ataxia and congenital glaucoma
MONDO:0009245	Friedreich ataxia
MONDO:0009244	Freesia Flowers, inability to smell
MONDO:0024881	secondary malignant neoplasm
MONDO:0024880	metastatic malignant neoplasm
MONDO:0009243	Fraser-like syndrome
MONDO:0009242	brittle cornea syndrome
MONDO:0010242	fetal akinesia syndrome, X-linked
MONDO:0009241	fountain syndrome
MONDO:0010241	congenital stationary night blindness 2A
MONDO:0010244	CGF1
MONDO:0009240	formiminoglutamic aciduria
MONDO:0010243	X-linked immunoneurologic disorder
MONDO:0010246	developmental and epileptic encephalopathy, 9
MONDO:0010245	X-linked cone-rod dystrophy 2
MONDO:0010248	X-linked spondyloepimetaphyseal dysplasia
MONDO:0010247	X-linked cerebral adrenoleukodystrophy
MONDO:0034217	resistance to thyroid hormone due to a mutation in thyroid hormone receptor beta
MONDO:0024879	metastatic carcinoma
MONDO:0034216	resistance to thyroid hormone due to a mutation in thyroid hormone receptor alpha
MONDO:0034212	methotrexate toxicity
MONDO:0036870	lymphatic vessel neoplasm
MONDO:0010240	androgen insensitivity syndrome
MONDO:0024873	clitoral carcinoma
MONDO:0024876	tendon sheath disorder
MONDO:0024878	secondary carcinoma
MONDO:0024877	clitoris neoplasm
MONDO:0010228	deafness, X-linked 3
MONDO:0010227	retinitis pigmentosa 3
MONDO:0009259	gamma-glutamylcysteine synthetase deficiency
MONDO:0012889	sarcoidosis, susceptibility to, 3
MONDO:0010229	alopecia, congenital
MONDO:0009258	classic galactosemia
MONDO:0009257	galactose epimerase deficiency
MONDO:0009256	galactorrhea
MONDO:0009255	galactokinase deficiency
MONDO:0009254	fucosidosis
MONDO:0009253	Fryns syndrome
MONDO:0012894	osteoarthritis susceptibility 6
MONDO:0010231	intellectual disability, X-linked 20
MONDO:0010230	intellectual disability, X-linked 23
MONDO:0009252	essential fructosuria
MONDO:0012895	torsion dystonia 17
MONDO:0010233	heterotopia, periventricular, X-linked dominant
MONDO:0009251	fructose-1,6-bisphosphatase deficiency
MONDO:0012892	bone fragility with contractures, arterial rupture, and deafness
MONDO:0012893	osteoarthritis susceptibility 5
MONDO:0010232	intestinal pseudoobstruction, neuronal, chronic idiopathic, X-linked
MONDO:0009250	fructose utilization
MONDO:0010235	X-linked intellectual disability-psychosis-macroorchidism syndrome
MONDO:0012898	narcolepsy 4, susceptibility to
MONDO:0012899	alopecia, androgenetic, 3
MONDO:0010234	body length, mouse, human homolog
MONDO:0010237	X-linked intellectual disability-plagiocephaly syndrome
MONDO:0012896	psoriasis 10, susceptibility to
MONDO:0012897	congenital factor XI deficiency
MONDO:0010236	intellectual disability, X-linked 14
MONDO:0024868	metastatic carcinoma in the adrenal medulla
MONDO:0022208	crystal arthropathy
MONDO:0012890	pontocerebellar hypoplasia type 2B
MONDO:0012891	pontocerebellar hypoplasia type 2C
MONDO:0000894	mucinous bronchioloalveolar adenocarcinoma
MONDO:0024861	mixed teratoma and seminoma
MONDO:0000893	mixed mucinous and nonmucinous bronchioloalveolar adenocarcinoma
MONDO:0000892	colon medullary carcinoma
MONDO:0024863	small size posterior uveal melanoma
MONDO:0022200	treatment for disease
MONDO:0000891	mixed fibrolamellar hepatocellular carcinoma
MONDO:0022201	has treatment by surgery
MONDO:0000898	malignant hemangioma
MONDO:0022202	disseminated
MONDO:0024864	medium/large size posterior uveal melanoma
MONDO:0000897	chronic myelomonocytic leukemia
MONDO:0000896	chronic neutrophilic leukemia
MONDO:0009229	hyaline fibromatosis syndrome
MONDO:0022205	pustular psoriasis
MONDO:0000895	nonmucinous bronchioloalveolar adenocarcinoma
MONDO:0009228	gingival fibromatosis-facial dysmorphism syndrome
MONDO:0010217	de Sanctis-Cacchione syndrome
MONDO:0009227	myofibromatosis, infantile, 1
MONDO:0010216	xeroderma pigmentosum group G
MONDO:0009226	fibrochondrogenesis 1
MONDO:0012878	Cowden syndrome 2
MONDO:0010219	xylosidase deficiency
MONDO:0010218	46,XX sex reversal 2
MONDO:0012879	schizophrenia 14
MONDO:0009225	fever, familial lifelong persistent
MONDO:0009224	fetal iodine syndrome
MONDO:0000890	Zika virus congenital syndrome
MONDO:0009223	hypogonadotropic hypogonadism 23 with or without anosmia
MONDO:0009222	Gollop-Wolfgang complex
MONDO:0009221	femur-fibula-ulna complex
MONDO:0010220	Young syndrome
MONDO:0012883	acute promyelocytic leukemia
MONDO:0009220	visceral steatosis, congenital
MONDO:0012884	systemic lupus erythematosus, susceptibility to, 13
MONDO:0010222	X-linked Opitz G/BBB syndrome
MONDO:0012881	major affective disorder 7
MONDO:0010221	CHIME syndrome
MONDO:0012882	major affective disorder 9
MONDO:0010224	corpus callosum agenesis-abnormal genitalia syndrome
MONDO:0012887	inflammatory bowel disease 23
MONDO:0012888	sarcoidosis, susceptibility to, 2
MONDO:0010223	ichthyosis, X-linked, without steroid sulfatase deficiency
MONDO:0012885	SRD5A3-CDG
MONDO:0010226	46,XY sex reversal 2
MONDO:0010225	Dent disease type 1
MONDO:0012886	inflammatory bowel disease 22
MONDO:0024857	immature extragonadal teratoma
MONDO:0000889	haemophilus meningitis
MONDO:0000888	gastrointestinal mucositis
MONDO:0012880	hypogonadotropic hypogonadism 5 with or without anosmia
MONDO:0012869	intellectual disability, autosomal dominant 22
MONDO:0010206	hypotrichosis 8
MONDO:0009239	hypogonadotropic hypogonadism 24 without anosmia
MONDO:0009238	hereditary folate malabsorption
MONDO:0010205	Wolman disease with hypolipoproteinemia and acanthocytosis
MONDO:0012867	hereditary spastic paraplegia 38
MONDO:0009237	focal epithelial hyperplasia
MONDO:0010208	wrinkly skin syndrome
MONDO:0009236	Kandori fleck retina
MONDO:0012868	thrombophilia due to protein S deficiency, autosomal dominant
MONDO:0010207	woolly hair-hypotrichosis-everted lower lip-outstanding ears syndrome
MONDO:0009235	familial benign flecked retina
MONDO:0010209	xanthinuria type I
MONDO:0009234	congenital high-molecular-weight kininogen deficiency
MONDO:0009233	Fibulo-ulnar hypoplasia-renal anomalies syndrome
MONDO:0009232	Fuhrmann syndrome
MONDO:0009231	fibular hypoplasia and complex brachydactyly
MONDO:0012872	thrombophilia, familial, due to decreased release of tissue plasminogen activator
MONDO:0009230	fibrosclerosis, multifocal
MONDO:0012873	Ehlers-Danlos syndrome, spondylocheirodysplastic type
MONDO:0012870	chromosome 2q31.2 deletion syndrome
MONDO:0010211	xeroderma pigmentosum group C
MONDO:0010210	xeroderma pigmentosum group A
MONDO:0012871	Jervell and Lange-Nielsen syndrome 2
MONDO:0010213	xeroderma pigmentosum group E
MONDO:0012876	heparin cofactor 2 deficiency
MONDO:0012877	major affective disorder 8
MONDO:0010212	xeroderma pigmentosum group D
MONDO:0010215	xeroderma pigmentosum group F
MONDO:0012874	porokeratosis 6, disseminated superficial actinic type
MONDO:0010214	xeroderma pigmentosum variant type
MONDO:0012875	inflammatory bowel disease 21
MONDO:0000899	malignant epithelioid hemangioendothelioma
MONDO:0009289	glycogen storage disease IC
MONDO:0009288	glycogen storage disease Ib
MONDO:0009287	glycogen storage disease due to glucose-6-phosphatase deficiency type IA
MONDO:0022263	congenital hepatic fibrosis
MONDO:0009286	gluteal muscles, absence of
MONDO:0010286	syndromic X-linked intellectual disability Siderius type
MONDO:0009285	gamma-glutamyl transpeptidase deficiency
MONDO:0010285	syndromic X-linked intellectual disability Abidi type
MONDO:0009284	glutathione synthetase deficiency without 5-oxoprolinuria
MONDO:0010288	adrenomyodystrophy
MONDO:0010287	hereditary spastic paraplegia 16
MONDO:0009283	glutaric acidemia type 3
MONDO:0009282	multiple acyl-CoA dehydrogenase deficiency
MONDO:0010289	intellectual disability, X-linked 72
MONDO:0009281	glutaryl-CoA dehydrogenase deficiency
MONDO:0009280	monosodium glutamate sensitivity
MONDO:0010280	ptosis, hereditary congenital 2
MONDO:0010282	mycobacterium tuberculosis, susceptibility to, X-linked
MONDO:0010281	Danon disease
MONDO:0010284	Armfield syndrome
MONDO:0010283	syndromic X-linked intellectual disability Lubs type
MONDO:0009299	46 XX gonadal dysgenesis
MONDO:0009298	GOMBO syndrome
MONDO:0010275	spondyloepimetaphyseal dysplasia, Bieganski type
MONDO:0009297	familial renal glucosuria
MONDO:0009296	glycoprotein storage disease
MONDO:0010274	testicular germ cell tumor 1
MONDO:0010277	syndromic X-linked intellectual disability Shashi type
MONDO:0009295	glycogen storage disease VII
MONDO:0009294	glycogen storage disease VI
MONDO:0010276	radioulnar synostosis, radial ray abnormalities, and severe malformations in the male
MONDO:0009293	glycogen storage disease V
MONDO:0010279	terminal osseous dysplasia-pigmentary defects syndrome
MONDO:0009292	glycogen storage disease due to glycogen branching enzyme deficiency
MONDO:0010278	Christianson syndrome
MONDO:0009291	glycogen storage disease III
MONDO:0009290	glycogen storage disease II
MONDO:0010271	X-linked myotubular myopathy-abnormal genitalia syndrome
MONDO:0010270	syndromic X-linked intellectual disability 7
MONDO:0010273	lymphoma, Hodgkin, X-linked pseudoautosomal
MONDO:0010272	syndromic X-linked intellectual disability type 10
MONDO:0009269	geleophysic dysplasia 1
MONDO:0009268	Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome
MONDO:0009267	Gaucher disease type III
MONDO:0009266	Gaucher disease type II
MONDO:0009265	Gaucher disease type I
MONDO:0010264	X-linked adrenal hypoplasia congenita
MONDO:0009264	gastroschisis
MONDO:0010263	Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome
MONDO:0009263	gapo syndrome
MONDO:0009262	GM1 gangliosidosis type 3
MONDO:0010266	intellectual disability, X-linked 58
MONDO:0009261	GM1 gangliosidosis type 2
MONDO:0010265	Simpson-Golabi-Behmel syndrome type 2
MONDO:0010268	X-linked lissencephaly with abnormal genitalia
MONDO:0009260	GM1 gangliosidosis type 1
MONDO:0010267	episodic muscle weakness, X-linked
MONDO:0010269	Coats disease
MONDO:0010260	arthrogryposis, congenital, lower limb, X-linked
MONDO:0010262	hypotonia, congenital nystagmus, ataxia, and abnormal auditory brainstem responses
MONDO:0010261	microphthalmia, syndromic 2
MONDO:0024893	toxocara canis infection (canine roundworms)
MONDO:0022236	colpocephaly
MONDO:0010249	X-linked B cell surface antigen, mouse, homolog-like 1
MONDO:0009279	triple-A syndrome
MONDO:0024890	pineal parenchymal cell neoplasm
MONDO:0009278	hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency
MONDO:0009277	glaucoma 3A
MONDO:0024892	soft tissue amyloid neoplasm
MONDO:0009276	Bernard-Soulier syndrome
MONDO:0024891	non-infectious meningitis
MONDO:0009275	neonatal hemochromatosis
MONDO:0010253	migraine, familial typical, susceptibility to, 2
MONDO:0010252	intellectual disability, X-linked, with panhypopituitarism
MONDO:0009274	ghosal hematodiaphyseal dysplasia
MONDO:0010255	diabetes mellitus, insulin-dependent, X-linked, susceptibility to
MONDO:0009273	hydatidiform mole, recurrent, 1
MONDO:0009272	German syndrome
MONDO:0010254	hematopoietic stem cell kinetics, control of
MONDO:0009271	geroderma osteodysplastica
MONDO:0010257	prostate cancer, hereditary, X-linked 1
MONDO:0010256	intellectual disability, X-linked 21
MONDO:0009270	genito-palato-cardiac syndrome
MONDO:0010259	retinitis pigmentosa 24
MONDO:0010258	MEHMO syndrome
MONDO:0034204	syndromic congenital sodium diarrhea
MONDO:0010251	intellectual disability, X-linked 50
MONDO:0010250	intellectual disability, X-linked 49
MONDO:0000832	myeloid neoplasm
MONDO:0000831	thrombotic disease
MONDO:0000830	Waldenstroem's macroglobulinemia
MONDO:0012814	diastasis recti and weakness of the linea alba
MONDO:0012815	Coats plus syndrome
MONDO:0012812	developmental and epileptic encephalopathy, 4
MONDO:0012813	retinitis pigmentosa 29
MONDO:0012818	maturity-onset diabetes of the young type 9
MONDO:0012819	diabetic ketoacidosis
MONDO:0012816	atrial fibrillation, familial, 6
MONDO:0012817	Ewing sarcoma
MONDO:0012821	colorectal cancer, susceptibility to, 5
MONDO:0012822	colorectal cancer, susceptibility to, 6
MONDO:0012820	colorectal cancer, susceptibility to, 3
MONDO:0000825	hypomyelinating leukodystrophy
MONDO:0000824	congenital diarrhea
MONDO:0000822	lymphoproliferative syndrome
MONDO:0000829	early-onset Parkinson disease
MONDO:0000828	juvenile-onset Parkinson disease
MONDO:0000827	salmonellosis
MONDO:0000826	syndromic X-linked intellectual disability Cabezas type
MONDO:0012809	histiocytoma, Angiomatoid fibrous
MONDO:0000841	metaphyseal dysplasia
MONDO:0000840	dysbaric osteonecrosis
MONDO:0012803	diarrhea-vomiting due to trehalase deficiency
MONDO:0012804	hypertrophic cardiomyopathy 12
MONDO:0012801	autism, susceptibility to, 15
MONDO:0012802	oculoauricular syndrome
MONDO:0012807	epidermolysis bullosa simplex with pyloric atresia
MONDO:0012808	dilated cardiomyopathy 1AA
MONDO:0012805	childhood onset GLUT1 deficiency syndrome 2
MONDO:0012806	ectodermal dysplasia and immunodeficiency 2
MONDO:0012810	aneurysm, intracranial berry, 7
MONDO:0012811	aneurysm, intracranial berry, 8
MONDO:0000836	disease of bone structure
MONDO:0000835	ischemic bone disease
MONDO:0000834	bone deterioration disease
MONDO:0000833	bone remodeling disease
MONDO:0000839	congenital abnormality
MONDO:0000838	chromosomal disease
MONDO:0000837	bone resorption disease
MONDO:0000810	DMD-related dilated cardiomyopathy
MONDO:0000809	purpura fulminans
MONDO:0000808	hepatoid adenocarcinoma
MONDO:0012800	trichoepithelioma, multiple familial, 2
MONDO:0000803	tiger prawn allergy
MONDO:0000802	Indian prawn allergy
MONDO:0000801	green mud crab allergy
MONDO:0000800	brown shrimp allergy
MONDO:0000807	latex allergy
MONDO:0000806	horned turban snail allergy
MONDO:0000805	snail allergy
MONDO:0000804	white shrimp allergy
MONDO:0000820	cerebral cavernous malformation
MONDO:0000819	anencephaly
MONDO:0000814	B-cell adult acute lymphocytic leukemia
MONDO:0000813	cardiac tuberculosis
MONDO:0000812	vertebral column disease
MONDO:0000811	anomalous left coronary artery from the pulmonary artery
MONDO:0000818	lethal congenital contracture syndrome 4
MONDO:0000816	abdominal obesity-metabolic syndrome
MONDO:0000815	fetal nicotine spectrum disorder
MONDO:0000872	B-cell childhood acute lymphoblastic leukemia
MONDO:0000871	T-cell childhood acute lymphocytic leukemia
MONDO:0000870	childhood acute lymphoblastic leukemia
MONDO:0000876	herpes simplex virus keratitis
MONDO:0000875	adult acute monocytic leukemia
MONDO:0009209	autosomal recessive faciodigitogenital syndrome
MONDO:0009208	faciothoracogenital syndrome
MONDO:0000874	T-cell childhood lymphoblastic lymphoma
MONDO:0000873	lymphoblastic lymphoma
MONDO:0009207	factor V and factor VIII, combined deficiency of, with normal protein C and protein C inhibitor
MONDO:0012858	primary CD59 deficiency
MONDO:0009206	factor V and factor VIII, combined deficiency of, type 1
MONDO:0009205	faciocardiorenal syndrome
MONDO:0012859	autosomal recessive osteopetrosis 7
MONDO:0012856	Birk-Barel syndrome
MONDO:0009204	lethal faciocardiomelic dysplasia
MONDO:0012857	porokeratosis 5, disseminated superficial actinic type
MONDO:0009203	focal facial dermal dysplasia type III
MONDO:0009202	Thakker-Donnai syndrome
MONDO:0009201	facial abnormalities, kyphoscoliosis, and intellectual disability
MONDO:0009200	eyebrow duplication-syndactyly syndrome
MONDO:0012861	premature ovarian failure 6
MONDO:0012862	attention deficit-hyperactivity disorder, susceptibility to, 5
MONDO:0010200	Wilson disease
MONDO:0012860	thrombophilia due to protein C deficiency, autosomal recessive
MONDO:0012865	Pseudofolliculitis barbae
MONDO:0010202	Wiskott-Aldrich syndrome
MONDO:0010201	Winchester syndrome
MONDO:0012866	hereditary spastic paraplegia 35
MONDO:0010204	lysosomal acid lipase deficiency
MONDO:0012863	attention deficit-hyperactivity disorder, susceptibility to, 6
MONDO:0012864	chromosome 2q32-q33 deletion syndrome
MONDO:0010203	intellectual disability, Wolff type
MONDO:0000869	congenital fibrosis of the extraocular muscles
MONDO:0000868	mitochondrial DNA depletion syndrome 6
MONDO:0000867	multiple pterygium syndrome
MONDO:0000866	myoglobinuria
MONDO:0000883	myeloid neoplasms associated with PDGFRB rearrangement
MONDO:0000882	myeloid and lymphoid neoplasms associated with PDGFRA rearrangement
MONDO:0000881	myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1
MONDO:0000880	lupus nephritis
MONDO:0000887	hepatic veno-occlusive disease
MONDO:0000886	meningococcal meningitis
MONDO:0009219	fascial dystrophy, congenital
MONDO:0000885	cloacal exstrophy
MONDO:0009218	Farber lipogranulomatosis
MONDO:0000884	myeloid and lymphoid neoplasms associated with FGFR1 abnormalities
MONDO:0012847	autosomal recessive congenital ichthyosis 6
MONDO:0009217	Fanconi-like syndrome
MONDO:0009216	glycogen storage disease due to GLUT2 deficiency
MONDO:0012848	Meckel syndrome, type 6
MONDO:0012845	inflammatory bowel disease 19
MONDO:0009215	Fanconi anemia complementation group A
MONDO:0012846	generalized epilepsy with febrile seizures plus, type 6
MONDO:0009214	Fanconi anemia complementation group D2
MONDO:0009213	Fanconi anemia complementation group C
MONDO:0009212	congenital factor X deficiency
MONDO:0009211	congenital factor VII deficiency
MONDO:0012849	Joubert syndrome 9
MONDO:0009210	congenital factor V deficiency
MONDO:0012850	hypophosphatemic nephrolithiasis/osteoporosis 1
MONDO:0012851	hypophosphatemic nephrolithiasis/osteoporosis 2
MONDO:0012854	bilateral microtia-deafness-cleft palate syndrome
MONDO:0012855	Joubert syndrome 8
MONDO:0012852	inflammatory bowel disease 20
MONDO:0012853	Fontaine progeroid syndrome
MONDO:0000879	cutaneous candidiasis
MONDO:0000878	cytomegalovirus retinitis
MONDO:0000877	Cryptococcal meningitis
MONDO:0000850	hypochondroplasia
MONDO:0000854	Stickler syndrome
MONDO:0000853	Kniest dysplasia
MONDO:0000852	hypochondrogenesis
MONDO:0000851	achondrogenesis
MONDO:0012836	systemic lupus erythematosus, susceptibility to, 12
MONDO:0012837	inflammatory bowel disease 15
MONDO:0012834	systemic lupus erythematosus, susceptibility to, 10
MONDO:0012835	systemic lupus erythematosus, susceptibility to, 11
MONDO:0012838	inflammatory bowel disease 16
MONDO:0012839	pyogenic bacterial infections due to MyD88 deficiency
MONDO:0012840	inflammatory bowel disease 17
MONDO:0012843	epilepsy, childhood absence, susceptibility to, 5
MONDO:0012844	primary ciliary dyskinesia 8
MONDO:0012841	inflammatory bowel disease 18
MONDO:0012842	melanoma, cutaneous malignant, susceptibility to, 7
MONDO:0000847	pycnodysostosis
MONDO:0000846	craniodiaphyseal dysplasia
MONDO:0024813	pulmonary sulcus neoplasm
MONDO:0000845	fibrous dysplasia
MONDO:0000844	spondyloepimetaphyseal dysplasia
MONDO:0000849	fibrogenesis imperfecta ossium
MONDO:0000848	axial osteomalacia
MONDO:0000861	tubular aggregate myopathy
MONDO:0000860	neural tube defect
MONDO:0000865	congenital fiber-type disproportion
MONDO:0000864	congenital myopathy
MONDO:0000863	myopathy, lactic acidosis, and sideroblastic anemia
MONDO:0000862	reducing body myopathy
MONDO:0012825	extraskeletal myxoid chondrosarcoma
MONDO:0012826	scoliosis, isolated, susceptibility to, 4
MONDO:0012823	colorectal cancer, susceptibility to, 7
MONDO:0012824	hypomyelinating leukodystrophy 4
MONDO:0012829	inflammatory bowel disease 12
MONDO:0012827	scoliosis, isolated, susceptibility to, 5
MONDO:0012828	atrial fibrillation, familial, 7
MONDO:0012832	inflammatory bowel disease 14
MONDO:0012833	Crouzon syndrome-acanthosis nigricans syndrome
MONDO:0012830	chromosome 10q23 deletion syndrome
MONDO:0012831	inflammatory bowel disease 13
MONDO:0000858	neuronal intestinal dysplasia
MONDO:0000857	Charcot-Marie-Tooth disease type 7
MONDO:0000856	Charcot-Marie-Tooth disease type 6
MONDO:0000855	acromesomelic dysplasia
MONDO:0000859	spina bifida occulta
MONDO:0000909	Bartter disease type 4B
MONDO:0000908	arrhythmogenic right ventricular dysplasia 13
MONDO:0000907	amelogenesis imperfecta type 1C
MONDO:0000902	agenesis of the corpus callosum with peripheral neuropathy
MONDO:0000901	relapsed/refractory diffuse large B-cell lymphoma
MONDO:0000900	PTEN hamartoma tumor syndrome
MONDO:0000906	Alzheimer disease 5
MONDO:0000905	cortisone reductase deficiency
MONDO:0000904	complex cortical dysplasia with other brain malformations
MONDO:0000903	myoclonus-dystonia syndrome
MONDO:0000920	duodenum cancer
MONDO:0000919	ampulla of vater cancer
MONDO:0000918	endometritis
MONDO:0000913	hereditary spherocytosis type 2
MONDO:0000912	autosomal recessive nonsyndromic deafness 5
MONDO:0000911	dilated cardiomyopathy 1T
MONDO:0000910	retinitis pigmentosa 6
MONDO:0000917	thyroid lymphoma
MONDO:0000916	intestinal infectious disease
MONDO:0000914	cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 1
MONDO:0022293	vascular disorder of penis
MONDO:0010297	FG syndrome 2
MONDO:0010296	immunodeficiency 61
MONDO:0010299	hypoxanthine guanine phosphoribosyltransferase partial deficiency
MONDO:0010298	Lesch-Nyhan syndrome
MONDO:0010291	androgen insensitivity syndrome due to coactivator deficiency
MONDO:0010290	goiter, multinodular 2
MONDO:0010293	ectodermal dysplasia and immune deficiency
MONDO:0010292	Uruguay Faciocardiomusculoskeletal syndrome
MONDO:0010295	anhidrotic ectodermal dysplasia-immunodeficiency-osteopetrosis-lymphedema syndrome
MONDO:0010294	X-linked severe congenital neutropenia
MONDO:0000795	penicillin allergy
MONDO:0000794	beta-lactam allergy
MONDO:0000793	rainbow trout allergy
MONDO:0000792	zebrafish allergy
MONDO:0000799	crustacean allergy
MONDO:0022103	chronic prostatitis
MONDO:0000798	mollusc allergy
MONDO:0000797	goat milk allergy
MONDO:0000796	cow milk allergy
MONDO:0009129	dwarfism, proportionate, with hip dislocation
MONDO:0010118	inherited threoninemia
MONDO:0009128	dwarfism, intellectual disability, and eye abnormality
MONDO:0010117	3M syndrome 1
MONDO:0009127	dwarfism, low-birth-weight type, with unresponsiveness to growth hormone
MONDO:0012779	celiac disease, susceptibility to, 10
MONDO:0009126	duodenal atresia
MONDO:0010119	Glanzmann's thrombasthenia
MONDO:0000791	carp allergy
MONDO:0009125	dopamine beta-hydroxylase, plasma, thermolability of
MONDO:0009124	Dubowitz syndrome
MONDO:0000790	Atlantic salmon allergy
MONDO:0009123	dopamine beta-hydroxylase deficiency
MONDO:0009122	Dohle bodies and leukemia
MONDO:0010121	thrombocytopenia-absent radius syndrome
MONDO:0009121	von Voss-Cherstvoy syndrome
MONDO:0012784	autosomal recessive ataxia due to ubiquinone deficiency
MONDO:0010120	thrombocytopenia 3
MONDO:0012785	pyloric stenosis, infantile hypertrophic, 3
MONDO:0009120	diverticulosis of bowel, hernia, and retinal detachment
MONDO:0010123	absent thumb-short stature-immunodeficiency syndrome
MONDO:0012782	celiac disease, susceptibility to, 13
MONDO:0010122	congenital thrombotic thrombocytopenic purpura
MONDO:0012783	RFT1-CDG
MONDO:0010125	upper limb defect-eye and ear abnormalities syndrome
MONDO:0012788	coronary heart disease, susceptibility to, 9
MONDO:0012789	dystonia 16
MONDO:0010124	thumb, distal hyperextensibility of
MONDO:0012786	juvenile cataract-microcornea-renal glucosuria syndrome
MONDO:0010127	thymoma, familial
MONDO:0012787	hereditary spastic paraplegia 39
MONDO:0010126	thymic aplasia with fetal death
MONDO:0000789	Atlantic cod allergy
MONDO:0012780	celiac disease, susceptibility to, 11
MONDO:0012781	celiac disease, susceptibility to, 12
MONDO:0024757	cardiovascular neoplasm
MONDO:0010107	testicular regression syndrome
MONDO:0009139	dyssegmental dysplasia, Rolland-Desbuquois type
MONDO:0010106	testes, rudimentary
MONDO:0010109	tetraamelia with ectodermal dysplasia and lacrimal duct abnormalities
MONDO:0009138	dysosteosclerosis
MONDO:0012768	prostate cancer, hereditary, 11
MONDO:0012769	prostate cancer, hereditary, 14
MONDO:0010108	testicular germ cell tumor
MONDO:0009137	dysmyelination with jaundice
MONDO:0009136	dyskeratosis congenita, autosomal recessive 1
MONDO:0009135	anemia, congenital dyserythropoietic, type 1a
MONDO:0009134	congenital dyserythropoietic anemia type 2
MONDO:0009133	cerebellar ataxia, intellectual disability, and dysequilibrium
MONDO:0009132	dysautonomia-like disorder
MONDO:0010110	tetraamelia-multiple malformations syndrome
MONDO:0012773	Hunter-Macdonald syndrome
MONDO:0012774	chromosome 15q13.3 microdeletion syndrome
MONDO:0009131	Riley-Day syndrome
MONDO:0009130	Dyggve-Melchior-Clausen disease
MONDO:0012771	asthma-related traits, susceptibility to, 7
MONDO:0010112	thalamic degeneration, symmetric infantile
MONDO:0010111	odontotrichomelic syndrome
MONDO:0012772	Stevenson-Carey syndrome
MONDO:0010114	thanatophoric dysplasia, Glasgow variant
MONDO:0012777	celiac disease, susceptibility to, 8
MONDO:0010113	thalidomide susceptibility
MONDO:0012778	celiac disease, susceptibility to, 9
MONDO:0012775	thrombocytopenia 4
MONDO:0010116	thoracomelic dysplasia
MONDO:0010115	thoracic dysplasia-hydrocephalus syndrome
MONDO:0012776	celiac disease, susceptibility to, 7
MONDO:0034106	developmental and epileptic encephalopathy, 73
MONDO:0034104	global developmental delay-alopecia-macrocephaly-facial dysmorphism-structural brain anomalies syndrome
MONDO:0034103	infection-related hemolytic uremic syndrome
MONDO:0012770	prostate cancer, hereditary, 15
MONDO:0000773	Timothy grass allergy
MONDO:0000772	pollen allergy
MONDO:0000771	allergic respiratory disease
MONDO:0000770	shellfish allergy
MONDO:0024744	childhood choroid plexus neoplasm
MONDO:0000777	gastrointestinal allergy
MONDO:0000776	metal allergy
MONDO:0000775	drug allergy
MONDO:0009109	lysinuric protein intolerance
MONDO:0024746	immature teratoma
MONDO:0034109	congenital myopathy with reduced type 2 muscle fibers
MONDO:0009108	hyperdibasic aminoaciduria type 1
MONDO:0000774	autoimmune neuropathy
MONDO:0012759	camptodactyly syndrome, Guadalajara type 3
MONDO:0009107	diastrophic dysplasia
MONDO:0009106	diastematomyelia
MONDO:0012757	lung fibrosis-immunodeficiency-46,XX gonadal dysgenesis syndrome
MONDO:0009105	trichohepatoenteric syndrome
MONDO:0012758	prostate cancer, hereditary, 13
MONDO:0009104	Donnai-Barrow syndrome
MONDO:0009103	diaphragmatic hernia 2
MONDO:0009102	diaminopentanuria
MONDO:0009101	Wolfram syndrome 1
MONDO:0009100	IDDM 1
MONDO:0012762	catecholaminergic polymorphic ventricular tachycardia 2
MONDO:0034110	atypical Fanconi syndrome-neonatal hyperinsulinism syndrome
MONDO:0012763	epilepsy, childhood absence, susceptibility to, 6
MONDO:0010101	Teebi-Shaltout syndrome
MONDO:0012760	epilepsy, idiopathic generalized, susceptibility to, 5
MONDO:0010100	Tay-Sachs disease
MONDO:0012761	chromosome 3q29 microduplication syndrome
MONDO:0012766	hereditary spastic paraplegia 37
MONDO:0010103	teeth, fused
MONDO:0010102	taurodontia-absent teeth-sparse hair syndrome
MONDO:0012767	age related macular degeneration 11
MONDO:0012764	RIDDLE syndrome
MONDO:0036779	axillary neoplasm
MONDO:0010105	teratoma, pineal
MONDO:0010104	non-eruption of teeth-maxillary hypoplasia-genu valgum syndrome
MONDO:0012765	lymphatic malformation 2
MONDO:0000769	chicken egg allergy
MONDO:0000768	Zika fever
MONDO:0000767	nut midline carcinoma
MONDO:0000784	melon allergy
MONDO:0000783	orange allergy
MONDO:0000782	Indian plum allergy
MONDO:0000781	cherry allergy
MONDO:0000788	fish allergy
MONDO:0000787	tomato allergy
MONDO:0000786	plum allergy
MONDO:0000785	peach allergy
MONDO:0009119	diverticulosis, small-intestinal
MONDO:0012748	primary ciliary dyskinesia 7
MONDO:0009118	disseminated sclerosis with narcolepsy
MONDO:0012749	mesomelic dysplasia, camera type
MONDO:0009117	disorganization, mouse, homolog of
MONDO:0009116	lactose intolerance
MONDO:0012746	dilated cardiomyopathy 2A
MONDO:0012747	glycogen storage disease due to aldolase A deficiency
MONDO:0009115	congenital lactase deficiency
MONDO:0000780	apricot allergy
MONDO:0009114	congenital sucrase-isomaltase deficiency
MONDO:0009113	hemolytic anemia due to diphosphoglycerate mutase deficiency
MONDO:0009112	rhizomelic chondrodysplasia punctata type 2
MONDO:0009111	dihydropyrimidinuria
MONDO:0012751	aortic aneurysm, familial abdominal, 3
MONDO:0009110	dicarboxylic aminoaciduria
MONDO:0034121	NAD(P)HX dehydratase deficiency
MONDO:0012752	aneurysm, intracranial berry, 6
MONDO:0012750	lethal arthrogryposis-anterior horn cell disease syndrome
MONDO:0012755	episodic ataxia type 7
MONDO:0012756	proximal 16p11.2 microdeletion syndrome
MONDO:0012753	amyotrophic lateral sclerosis type 9
MONDO:0012754	nanophthalmos 3
MONDO:0034127	IgA pemphigus
MONDO:0000779	apple allergy
MONDO:0000778	fruit allergy
MONDO:0036781	benign axillary neoplasm
MONDO:0034122	NAD(P)HX epimerase deficiency
MONDO:0022145	Chiari malformation type II
MONDO:0009169	endocardial fibroelastosis
MONDO:0009168	Fowler syndrome
MONDO:0022140	Charles bonnet syndrome
MONDO:0009167	Bonnemann-Meinecke-Reich syndrome
MONDO:0009166	pontocerebellar hypoplasia type 4
MONDO:0009165	Aicardi-Goutieres syndrome 1
MONDO:0010165	ulna hypoplasia-intellectual disability syndrome
MONDO:0010164	phocomelia, Schinzel type
MONDO:0009164	encephalopathy, axonal, with necrotizing myopathy, cardiomyopathy, and cataracts
MONDO:0010167	urocanic aciduria
MONDO:0009163	encephalomalacia, multilocular
MONDO:0009162	Ellis-van Creveld syndrome
MONDO:0010166	ulnar agenesis and endocardial fibroelastosis
MONDO:0010169	Usher syndrome type 2A
MONDO:0009161	Ehlers-Danlos syndrome, dermatosparaxis type
MONDO:0010168	Usher syndrome type 1
MONDO:0009160	Ehlers-Danlos syndrome, type 6
MONDO:0010161	tyrosinemia type I
MONDO:0010160	tyrosinemia type II
MONDO:0010163	Tyrosinosis
MONDO:0010162	tyrosinemia type III
MONDO:0024797	adult brain stem neoplasm
MONDO:0009179	recessive dystrophic epidermolysis bullosa
MONDO:0009178	epidermolysis bullosa dystrophica Neurotrophica
MONDO:0009177	late-onset localized junctional epidermolysis bullosa-intellectual disability syndrome
MONDO:0010154	trigonocephaly-bifid nose-acral anomalies syndrome
MONDO:0009176	epidermodysplasia verruciformis
MONDO:0009175	eosinophilic fasciitis
MONDO:0010153	trichoodontoonychial dysplasia
MONDO:0009174	protein-losing enteropathy
MONDO:0010156	Troyer syndrome
MONDO:0010155	Dorfman-Chanarin disease
MONDO:0009173	congenital enteropathy due to enteropeptidase deficiency
MONDO:0009172	enterocolitis
MONDO:0010158	T-substance anomaly
MONDO:0009171	endothelial dystrophy, congenital hereditary, with nail hypoplasia
MONDO:0010157	Tryptophanuria with dwarfism
MONDO:0009170	endocardial fibroelastosis and coarctation of abdominal aorta
MONDO:0010159	mismatch repair cancer syndrome 1
MONDO:0010150	head and neck squamous cell carcinoma
MONDO:0010152	trichomegaly-retina pigmentary degeneration-dwarfism syndrome
MONDO:0010151	tricarboxylic acid cycle, defect of
MONDO:0010139	isolated thyroid-stimulating hormone deficiency
MONDO:0009149	ectodermal dysplasia-intellectual disability-central nervous system malformation syndrome
MONDO:0009148	Rosselli-Gulienetti syndrome
MONDO:0009147	ectodermal dysplasia 10B, hypohidrotic/hair/tooth type, autosomal recessive
MONDO:0009146	ectodermal dysplasia-sensorineural deafness syndrome
MONDO:0009145	SchC6pf-Schulz-Passarge syndrome
MONDO:0009144	Ebstein anomaly
MONDO:0010143	lethal restrictive dermopathy
MONDO:0009143	Meier-Gorlin syndrome 1
MONDO:0009142	dystonia with Ringbinden
MONDO:0010142	hypothyroidism due to TSH receptor mutations
MONDO:0009141	torsion dystonia 2
MONDO:0010145	tibia, absence of, with congenital deafness
MONDO:0009140	Silverman-Handmaker type dyssegmental dysplasia
MONDO:0010144	tibial hemimelia
MONDO:0010147	tongue, pigmented fungiform papillae of
MONDO:0010146	Kerion celsi
MONDO:0010149	transcobalamin II deficiency
MONDO:0010148	Mounier-Kuhn syndrome
MONDO:0010141	tiglic acidemia
MONDO:0010140	isolated thyrotropin-releasing hormone deficiency
MONDO:0022113	central centrifugal cicatricial alopecia
MONDO:0010129	thymic-renal-anal-lung dysplasia
MONDO:0010128	thyrocerebrorenal syndrome
MONDO:0009159	Ehlers-Danlos syndrome, cardiac valvular type
MONDO:0009158	Ehlers-Danlos syndrome, fibronectinemic type
MONDO:0009157	split hand-foot malformation 6
MONDO:0009156	ectrodactyly-polydactyly syndrome
MONDO:0009155	EEM syndrome
MONDO:0009154	hypothyroidism, congenital, nongoitrous, 5
MONDO:0010132	familial thyroid dyshormonogenesis
MONDO:0012795	hypophosphatemic rickets and hyperparathyroidism
MONDO:0010131	thyroid hormone resistance, generalized, autosomal recessive
MONDO:0012796	retinitis pigmentosa 41
MONDO:0009153	ectopia lentis et pupillae
MONDO:0009152	ectopia lentis 2, isolated, autosomal recessive
MONDO:0010134	Pendred syndrome
MONDO:0012793	hypouricemia, renal, 2
MONDO:0009151	cleft lip/palate-ectodermal dysplasia syndrome
MONDO:0010133	thyroid dyshormonogenesis 2A
MONDO:0012794	ANE syndrome
MONDO:0012799	hypertrophic cardiomyopathy 11
MONDO:0010136	thyroid dyshormonogenesis 4
MONDO:0009150	hypohidrotic ectodermal dysplasia-hypothyroidism-ciliary dyskinesia syndrome
MONDO:0010135	thyroid dyshormonogenesis 3
MONDO:0012797	otosclerosis 8
MONDO:0010138	thyrotoxicosis
MONDO:0010137	thyroid dyshormonogenesis 5
MONDO:0012798	deafness, unilateral, with delayed endolymphatic hydrops
MONDO:0022109	catatrichy
MONDO:0012791	mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria
MONDO:0012792	mitochondrial DNA depletion syndrome 8a
MONDO:0010130	dihydropyrimidine dehydrogenase deficiency
MONDO:0012790	amyotrophic lateral sclerosis type 10
MONDO:0000711	amyotrophic lateral sclerosis type 13
MONDO:0000710	gastroduodenal Crohn disease
MONDO:0000709	Crohn ileitis
MONDO:0012700	renal tubular acidosis, distal, 4, with hemolytic anemia
MONDO:0012701	cataract 12 multiple types
MONDO:0000704	lymphocytic colitis
MONDO:0000703	collagenous colitis
MONDO:0000702	microscopic colitis
MONDO:0000701	ischemic colitis
MONDO:0000708	Crohn jejunoileitis
MONDO:0000707	diversion colitis
MONDO:0000706	chemical colitis
MONDO:0000705	Clostridium difficile colitis
MONDO:0000722	non-syndromic synpolydactyly
MONDO:0000721	xanthinuria
MONDO:0000720	basal ganglia calcification
MONDO:0000715	lymph node adenoid cystic carcinoma
MONDO:0000714	crest syndrome
MONDO:0000713	Balo concentric sclerosis
MONDO:0000712	FTDALS
MONDO:0000719	Baraitser-winter syndrome
MONDO:0000718	Adams-Oliver syndrome
MONDO:0000717	acrofrontofacionasal dysostosis
MONDO:0000716	agraphia
MONDO:0000700	familial hemiplegic migraine
MONDO:0000751	cervical polyp
MONDO:0000750	dental abscess
MONDO:0000755	ectopic pregnancy
MONDO:0000754	anal fistula
MONDO:0000753	omphalocele
MONDO:0000752	myelomeningocele
MONDO:0012737	long QT syndrome 10
MONDO:0012738	long QT syndrome 11
MONDO:0012735	Temple-Baraitser syndrome
MONDO:0012736	long QT syndrome 9
MONDO:0012739	microtia-eye coloboma-imperforation of the nasolacrimal duct syndrome
MONDO:0012740	chromosome 22q11.2 deletion syndrome, distal
MONDO:0012741	prostate cancer, hereditary, 12
MONDO:0012744	dilated cardiomyopathy 1Y
MONDO:0012745	dilated cardiomyopathy 1Z
MONDO:0012742	Brugada syndrome 3
MONDO:0012743	Brugada syndrome 4
MONDO:0000748	mastoiditis
MONDO:0024715	benign synovial neoplasm
MONDO:0000747	umbilical hernia
MONDO:0000746	inguinal hernia
MONDO:0000745	cardiac arrest
MONDO:0000749	breast abscess
MONDO:0000762	syndrome caused by partial chromosomal duplication
MONDO:0000761	syndrome caused by partial chromosomal deletion
MONDO:0000760	acrofacial dysostosis
MONDO:0000766	corneal endothelial dystrophy
MONDO:0024711	malignant mixed epithelial stromal tumor of the kidney
MONDO:0000765	corneal stromal dystrophy
MONDO:0000764	epithelial-stromal TGFBI dystrophy
MONDO:0000763	epithelial and subepithelial corneal dystrophy
MONDO:0012726	autosomal dominant familial hematuria-retinal arteriolar tortuosity-contractures syndrome
MONDO:0012727	mucocutaneous lymph node syndrome
MONDO:0012724	familial cold autoinflammatory syndrome 2
MONDO:0012725	lipoprotein glomerulopathy
MONDO:0012728	Brugada syndrome 2
MONDO:0012729	erythrocytosis, familial, 4
MONDO:0012730	aortic aneurysm, familial thoracic 6
MONDO:0012733	autosomal recessive bestrophinopathy
MONDO:0012734	SERKAL syndrome
MONDO:0012731	elliptocytosis 1
MONDO:0012732	tremor, hereditary essential, and idiopathic normal pressure hydrocephalus
MONDO:0000759	acrorenal syndrome
MONDO:0000758	bacillary angiomatosis
MONDO:0000757	glucocorticoid-induced osteoporosis
MONDO:0000756	parameningeal embryonal rhabdomyosarcoma
MONDO:0000733	cornea plana
MONDO:0000732	combined oxidative phosphorylation deficiency
MONDO:0000731	peeling skin syndrome
MONDO:0000730	pontocerebellar hypoplasia
MONDO:0012715	migraine with or without aura, susceptibility to, 12
MONDO:0012716	spondyloepiphyseal dysplasia, Cantu type
MONDO:0012713	spondylometaphyseal dysplasia, East African type
MONDO:0012714	early-onset myopathy with fatal cardiomyopathy
MONDO:0012719	encephalopathy due to prosaposin deficiency
MONDO:0012717	renal hypomagnesemia 4
MONDO:0012718	hypotonia with lactic acidemia and hyperammonemia
MONDO:0012722	Dauwerse-Peters syndrome
MONDO:0012723	Leber congenital amaurosis 10
MONDO:0012720	Krabbe disease, atypical, due to saposin A deficiency
MONDO:0012721	progressive myoclonic epilepsy type 3
MONDO:0000726	idiopathic scoliosis
MONDO:0000725	Simpson-Golabi-Behmel syndrome
MONDO:0000724	specific language impairment
MONDO:0000723	stutter disorder
MONDO:0000729	congenital ptosis
MONDO:0000728	ptosis
MONDO:0000727	scapuloperoneal myopathy
MONDO:0000740	adenoid hypertrophy
MONDO:0000744	lung abscess
MONDO:0000743	oral hairy leukoplakia
MONDO:0000742	persistent generalized lymphadenopathy
MONDO:0000741	angular cheilitis
MONDO:0012704	dilated cardiomyopathy 1X
MONDO:0012705	familial temporal lobe epilepsy 3
MONDO:0012702	celiac disease, susceptibility to, 6
MONDO:0012703	lissencephaly due to TUBA1A mutation
MONDO:0012708	primary lateral sclerosis, adult, 1
MONDO:0012709	microphthalmia, isolated, with coloboma 5
MONDO:0012706	familial temporal lobe epilepsy 4
MONDO:0012707	familial febrile seizures 9
MONDO:0012711	peripapillary atrophy, beta type
MONDO:0012712	dystonia with cerebellar atrophy
MONDO:0012710	hirschsprung disease, susceptibility to, 9
MONDO:0000737	megalocornea
MONDO:0000736	dyschromatosis universalis hereditaria
MONDO:0000735	oculodentodigital dysplasia
MONDO:0000734	Ohdo syndrome and variants
MONDO:0000739	uvulitis
MONDO:0000738	syndromic X-linked intellectual disability
MONDO:0022180	chromosome 16 trisomy
MONDO:0022177	chromosome 13q trisomy
MONDO:0022178	chromosome 13q-mosaicism
MONDO:0022171	chromhidrosis
MONDO:0022173	chromosome 11q trisomy
MONDO:0022174	chromosome 12p deletion
MONDO:0010198	Wernicke-Korsakoff syndrome
MONDO:0010197	whistling face syndrome, recessive form
MONDO:0034186	autosomal recessive extra-oral halitosis
MONDO:0010199	white forelock with malformations
MONDO:0010190	pontocerebellar hypoplasia type 2A
MONDO:0010192	Waardenburg syndrome type 4A
MONDO:0010191	von Willebrand disease 3
MONDO:0010194	Weill-Marchesani syndrome 1
MONDO:0010193	Weaver syndrome
MONDO:0010196	Werner syndrome
MONDO:0034189	primary biliary cholangitis/primary sclerosing cholangitis and autoimmune hepatitis overlap syndrome
MONDO:0010195	Weissenbacher-Zweymuller syndrome
MONDO:0009189	multiple epiphyseal dysplasia type 4
MONDO:0009188	epilepsy-telangiectasia syndrome
MONDO:0010187	vitamin K-dependent clotting factors, combined deficiency of, type 1
MONDO:0009187	celiac disease-epilepsy-cerebral calcification syndrome
MONDO:0010186	vitamin D-dependent rickets, type 2A
MONDO:0009186	epilepsy, photogenic, with spastic diplegia and intellectual disability
MONDO:0010189	vitiligo, progressive, with intellectual disability and urethral duplication
MONDO:0009185	amelocerebrohypohidrotic syndrome
MONDO:0010188	familial isolated deficiency of vitamin E
MONDO:0009184	epidermolysis bullosa with diaphragmatic hernia
MONDO:0009183	junctional epidermolysis bullosa with pyloric atresia
MONDO:0009182	junctional epidermolysis bullosa Herlitz type
MONDO:0009181	epidermolysis bullosa simplex with muscular dystrophy
MONDO:0009180	junctional epidermolysis bullosa, non-Herlitz type
MONDO:0010181	oculogastrointestinal muscular dystrophy
MONDO:0010180	autosomal recessive spondylocostal dysostosis
MONDO:0010183	methylmalonic aciduria and homocystinuria type cblF
MONDO:0010182	hypercarotenemia and vitamin A deficiency, autosomal recessive
MONDO:0010185	methylmalonic aciduria and homocystinuria type cblD
MONDO:0010184	methylmalonic aciduria and homocystinuria type cblC
MONDO:0022151	Chitty Hall Webb syndrome
MONDO:0009199	ethanolaminosis
MONDO:0009198	congenital lethal erythroderma
MONDO:0010176	orofaciodigital syndrome type 6
MONDO:0010175	van Bogaert-Hozay syndrome
MONDO:0009197	transient erythroblastopenia of childhood
MONDO:0009196	ermine phenotype
MONDO:0010178	congenital bilateral aplasia of vas deferens from CFTR mutation
MONDO:0010177	vascular hyalinosis
MONDO:0009195	erythema of acral regions
MONDO:0009194	immunodeficiency 32B
MONDO:0009193	epithelial squamous dysplasia, keratinizing desquamative, of urinary tract
MONDO:0010179	isolated right ventricular hypoplasia
MONDO:0009192	Wolcott-Rallison syndrome
MONDO:0009191	Lowry-Wood syndrome
MONDO:0009190	epiphyseal dysplasia of femoral head, myopia, and deafness
MONDO:0010170	Usher syndrome type 3A
MONDO:0010172	VACTERL with hydrocephalus
MONDO:0010171	Usher syndrome type 1C
MONDO:0010174	Valinemia
MONDO:0010173	Mayer-Rokitansky-Kuster-Hauser syndrome type 1
MONDO:0034143	early-onset calcifying leukoencephalopathy-skeletal dysplasia
MONDO:0034142	pancreatic agenesis-holoprosencephaly syndrome
MONDO:0034147	neonatal epileptic encephalopathy due to glutaminase deficiency
MONDO:0034146	spastic ataxia-dysarthria due to glutaminase deficiency
MONDO:0034145	oculocerebrodental syndrome
MONDO:0034150	idiopathic gastroparesis
MONDO:0022196	chronic erosive gastritis
MONDO:0000674	mirror agnosia
MONDO:0000673	integrative agnosia
MONDO:0000672	form agnosia
MONDO:0024643	myocardial disorder
MONDO:0024642	gastric neuroendocrine tumor G2
MONDO:0000671	finger agnosia
MONDO:0000678	simultanagnosia
MONDO:0024645	retroperitoneal neoplasm
MONDO:0024644	myocardial ischemia
MONDO:0000677	semantic agnosia
MONDO:0024647	urolithiasis
MONDO:0000676	phonagnosia
MONDO:0024646	refractory
MONDO:0000675	pain agnosia
MONDO:0009009	hypoplasminogenemia
MONDO:0009008	heart defect - tongue hamartoma - polysyndactyly syndrome
MONDO:0009007	Jalili syndrome
MONDO:0009006	complement component 2 deficiency
MONDO:0012658	brachydactyly type B2
MONDO:0012659	age related macular degeneration 9
MONDO:0009005	complement component C1r/C1s deficiency
MONDO:0000670	cortical deafness
MONDO:0009004	combined inflammatory and immunologic defect
MONDO:0009003	achromatopsia 2
MONDO:0009002	coloboma, ocular, autosomal recessive
MONDO:0009001	macular coloboma-cleft palate-hallux valgus syndrome
MONDO:0009000	familial reactive perforating collagenosis
MONDO:0010000	rod-cone dystrophy, sensorineural deafness, and Fanconi-type renal dysfunction
MONDO:0012663	Plasmodium falciparum fever episodes quantitative trait locus 1
MONDO:0012664	spastic ataxia 3
MONDO:0012661	susceptibility to visceral leishmaniasis, 3
MONDO:0010002	Rothmund-Thomson syndrome
MONDO:0010001	ectodermal dysplasia-blindness syndrome
MONDO:0012662	Usher syndrome type 2D
MONDO:0010004	EEC syndrome
MONDO:0012667	dilated cardiomyopathy 1W
MONDO:0010003	Rowley-Rosenberg syndrome
MONDO:0012668	Tented eyebrows
MONDO:0010006	Sandhoff disease
MONDO:0012665	cataract 33
MONDO:0010005	saccharopinuria
MONDO:0012666	asthma-related traits, susceptibility to, 6
MONDO:0024638	pancreatic gastrinoma
MONDO:0024637	malignant soft tissue neoplasm
MONDO:0000669	color agnosia
MONDO:0024639	gastric enterochromaffin cell serotonin-producing neuroendocrine tumor
MONDO:0000668	autotopagnosia
MONDO:0012660	susceptibility to visceral leishmaniasis, 2
MONDO:0000685	visual agnosia
MONDO:0024630	defective phagocytic cell chemotaxis
MONDO:0000684	verbal auditory agnosia
MONDO:0024632	defective phagocytic cell opsonization
MONDO:0000683	topographical agnosia
MONDO:0000682	time agnosia
MONDO:0024634	large intestine disease
MONDO:0000689	survival motor neuron spinal muscular atrophy
MONDO:0000688	inherited organic acidemia
MONDO:0024633	hypertensive nephropathy
MONDO:0024636	inflammation of heart layer
MONDO:0000687	diffuse alopecia areata
MONDO:0000686	alexia without agraphia
MONDO:0024635	small intestine disease
MONDO:0009019	congenital hereditary endothelial dystrophy of cornea
MONDO:0012649	FTSD
MONDO:0009018	central cloudy dystrophy of François
MONDO:0009017	corneal degeneration, band-shaped spheroid
MONDO:0012647	generalized epilepsy with febrile seizures plus, type 3
MONDO:0012648	isobutyryl-CoA dehydrogenase deficiency
MONDO:0009016	band keratopathy
MONDO:0009015	corneal dystrophy-perceptive deafness syndrome
MONDO:0000681	tactile agnosia
MONDO:0000680	astereognosia
MONDO:0009014	cornea plana 2
MONDO:0009013	convulsive disorder, familial, with prenatal or early onset
MONDO:0009012	multiple pterygium-malignant hyperthermia syndrome
MONDO:0009011	constriction rings syndrome
MONDO:0012652	autosomal recessive limb-girdle muscular dystrophy type 2L
MONDO:0012653	persistent hyperplastic primary vitreous, autosomal dominant
MONDO:0009010	aortic arch interruption
MONDO:0012650	Cernunnos-XLF deficiency
MONDO:0012651	spastic ataxia 2
MONDO:0012656	lethal congenital contracture syndrome 3
MONDO:0012657	Mungan syndrome
MONDO:0012654	atrial septal defect 4
MONDO:0012655	myoclonic epilepsy, juvenile, susceptibility to, 4
MONDO:0024627	phagocytic cell dysfunction
MONDO:0024626	defective phagocytic cell engulfment
MONDO:0000679	social emotional agnosia
MONDO:0000652	integumentary system benign neoplasm
MONDO:0000651	thoracic disease
MONDO:0000650	peritoneal benign neoplasm
MONDO:0024621	serous cystadenocarcinoma
MONDO:0024620	meningitis caused by poliovirus
MONDO:0024623	otorhinolaryngologic disease
MONDO:0000656	alpha chain disease
MONDO:0024622	thyroid gland adenocarcinoma
MONDO:0000655	heavy chain disease
MONDO:0024625	disorder of lacrimal gland
MONDO:0000654	benign connective and soft tissue neoplasm
MONDO:0000653	integumentary system cancer
MONDO:0024624	atrophy of lacrimal gland
MONDO:0012638	microphthalmia-brain atrophy syndrome
MONDO:0012639	hereditary spastic paraplegia 18
MONDO:0012636	restless legs syndrome, susceptibility to, 6
MONDO:0012637	COG1-CDG
MONDO:0012641	restless legs syndrome, susceptibility to, 5
MONDO:0012642	major affective disorder 4
MONDO:0012640	Charcot-Marie-Tooth disease type 4J
MONDO:0012645	glaucoma 1, open angle, N
MONDO:0012646	glaucoma 1, open angle, H
MONDO:0012643	hereditary spastic paraplegia 32
MONDO:0012644	asphyxiating thoracic dystrophy 2
MONDO:0000649	sensory system cancer
MONDO:0024616	tympanitis
MONDO:0000648	nervous system benign neoplasm
MONDO:0024615	T-cell and NK-cell neoplasm
MONDO:0024618	poliovirus infection
MONDO:0000647	benign vaginal neoplasm
MONDO:0000646	ovarian benign neoplasm
MONDO:0024617	xanthogranuloma
MONDO:0024619	central nervous system infectious disorder
MONDO:0000663	anosognosia
MONDO:0000662	amusia
MONDO:0024610	parasitic skin disease
MONDO:0000661	alexithymia
MONDO:0000660	akinetopsia
MONDO:0024612	manic bipolar affective disorder
MONDO:0000667	auditory agnosia
MONDO:0024611	orbit neoplasm
MONDO:0000666	associative visual agnosia
MONDO:0000665	apraxia
MONDO:0024614	neurotic depression
MONDO:0024613	bipolar depression
MONDO:0000664	apperceptive agnosia
MONDO:0012627	epilepsy, idiopathic generalized, susceptibility to, 13
MONDO:0012628	coronary heart disease, susceptibility to, 8
MONDO:0012625	retinitis pigmentosa 37
MONDO:0012626	Meckel syndrome, type 4
MONDO:0012629	paroxysmal nonkinesigenic dyskinesia 2
MONDO:0012630	Alzheimer disease 13
MONDO:0012631	Alzheimer disease 14
MONDO:0012634	craniofacial dysplasia - osteopenia syndrome
MONDO:0012635	COG8-CDG
MONDO:0012632	Alzheimer disease 15
MONDO:0012633	malaria
MONDO:0000659	delta-heavy chain disease
MONDO:0024607	congenital muscular dystrophy with cataracts and intellectual disability
MONDO:0000658	mu chain disease
MONDO:0000657	gamma heavy chain disease
MONDO:0024609	vulvar squamous cell carcinoma
MONDO:0024608	dientamoebiasis
MONDO:0024685	Philadelphia-positive myelogenous leukemia
MONDO:0022022	bowenoid papulosis
MONDO:0022025	boylan dew greco syndrome
MONDO:0024686	tenosynovial giant cell tumor, diffuse type
MONDO:0009049	Cushing syndrome due to macronodular adrenal hyperplasia
MONDO:0009048	curved nail of fourth toe
MONDO:0009047	cryptorchidism
MONDO:0009046	Fraser syndrome
MONDO:0022020	Boudhina Yedes Khiari syndrome
MONDO:0009045	cataract-nephropathy-encephalopathy syndrome
MONDO:0010044	hereditary spastic paraplegia 15
MONDO:0009044	Crigler-Najjar syndrome
MONDO:0009043	generalized resistance to thyroid hormone
MONDO:0010043	hereditary spastic paraplegia 17
MONDO:0010046	hereditary spastic paraplegia 23
MONDO:0009042	craniotelencephalic dysplasia
MONDO:0010045	paraplegia-brachydactyly-cone-shaped epiphysis syndrome
MONDO:0009041	craniosynostosis-intellectual disability-clefting syndrome
MONDO:0010048	spastic paraplegia with myoclonic epilepsy
MONDO:0009040	craniosynostosis-intellectual disability syndrome of 51N and Gettig
MONDO:0010047	hereditary spastic paraplegia 5A
MONDO:0010049	spastic paraplegia-glaucoma-intellectual disability syndrome
MONDO:0010040	ataxia, spastic, childhood-onset, autosomal recessive, with optic atrophy and intellectual disability
MONDO:0010042	spastic diplegia and intellectual disability
MONDO:0010041	Charlevoix-Saguenay spastic ataxia
MONDO:0024674	Pancoast syndrome
MONDO:0022011	bobble-head doll syndrome
MONDO:0024673	skin lymphangioma
MONDO:0022013	Boerhaave syndrome
MONDO:0024676	childhood kidney Wilms tumor
MONDO:0024675	adult kidney Wilms tumor
MONDO:0024677	pancreatic insulinoma
MONDO:0022018	Borrone di Rocco Crovato syndrome
MONDO:0010029	situs inversus
MONDO:0009059	cysteine Peptiduria
MONDO:0009058	cystathioninuria
MONDO:0009057	cyanosis and hepatic disease
MONDO:0009056	cutis verticis gyrata and intellectual disability
MONDO:0009055	cutis marmorata telangiectatica congenita
MONDO:0010033	generalized peeling skin syndrome
MONDO:0012696	otosclerosis 4
MONDO:0010032	Sjogren-Larsson-like ichthyosis without CNS or eye involvement
MONDO:0009054	autosomal recessive cutis laxa type 2, classic type
MONDO:0012697	otosclerosis 7
MONDO:0012694	Joubert syndrome 7
MONDO:0010035	Smith-Lemli-Opitz syndrome
MONDO:0009053	ALDH18A1-related de Barsy syndrome
MONDO:0009052	cutis laxa, autosomal recessive, type 1A
MONDO:0012695	Meckel syndrome, type 5
MONDO:0010034	anosmia for butyl mercaptan
MONDO:0009051	cutaneous photosensitivity-lethal colitis syndrome
MONDO:0010037	sodium-potassium-ATPase activity of red cell
MONDO:0010036	congenital secretory sodium diarrhea 3
MONDO:0009050	Cushing disease due to pituitary adenoma
MONDO:0012698	Waardenburg syndrome type 2E
MONDO:0010039	congenital heart defect-round face-developmental delay syndrome
MONDO:0012699	autosomal recessive limb-girdle muscular dystrophy type 2M
MONDO:0010038	growth delay due to insulin-like growth factor I resistance
MONDO:0012692	renal tubular acidosis, distal, with nephrocalcinosis, short stature, intellectual disability, and distinctive facies
MONDO:0012693	glycogen storage disease due to muscle and heart glycogen synthase deficiency
MONDO:0012690	Noonan syndrome 5
MONDO:0010031	Sjogren-Larsson syndrome
MONDO:0012691	LEOPARD syndrome 2
MONDO:0010030	Sjogren syndrome
MONDO:0024663	primary skin meningioma
MONDO:0000696	juvenile absence epilepsy
MONDO:0024662	colorectal tubulovillous adenoma
MONDO:0000695	histidinemia
MONDO:0024665	indeterminate sex and/or pseudohermaphroditism
MONDO:0000694	seasonal affective disorder
MONDO:0024664	hypertension, pregnancy-induced
MONDO:0000693	bipolar II disorder
MONDO:0024666	benign epithelial skin neoplasm
MONDO:0000699	homocarnosinosis
MONDO:0000698	gamma-amino butyric acid metabolism disorder
MONDO:0022007	water intoxication
MONDO:0000697	succinic semialdehyde dehydrogenase deficiency
MONDO:0010019	secretory component deficiency
MONDO:0009029	cranial nerves, congenital paresis of
MONDO:0010018	second metatarsal-metacarpal syndrome
MONDO:0009028	Crane-Heise syndrome
MONDO:0009027	cramps, familial adolescent
MONDO:0009026	Costello syndrome
MONDO:0000692	Kleine-Levin syndrome
MONDO:0009025	apparent mineralocorticoid excess
MONDO:0000691	pain disorder
MONDO:0000690	body dysmorphic disorder
MONDO:0024661	tubulovillous adenoma
MONDO:0009024	cortical blindness-intellectual disability-polydactyly syndrome
MONDO:0024660	tubular adenoma
MONDO:0009023	hereditary motor and sensory neuropathy with agenesis of the corpus callosum
MONDO:0012685	major affective disorder 5
MONDO:0010022	senile plaque formation
MONDO:0009022	corpus callosum, agenesis of
MONDO:0012686	major affective disorder 6
MONDO:0009021	Toriello-Carey syndrome
MONDO:0010021	seizures, benign familial neonatal, autosomal recessive
MONDO:0010024	Beemer-Langer syndrome
MONDO:0009020	macular corneal dystrophy
MONDO:0012683	pontocerebellar hypoplasia type 6
MONDO:0010023	combined immunodeficiency due to ZAP70 deficiency
MONDO:0012684	arrhythmogenic right ventricular dysplasia 12
MONDO:0012689	premature ovarian failure 5
MONDO:0010026	SHORT syndrome
MONDO:0010025	short stature-obesity syndrome
MONDO:0010028	sialuria
MONDO:0012687	familial cavitary optic disc anomaly
MONDO:0012688	cataract 17 multiple types
MONDO:0010027	free sialic acid storage disease, infantile form
MONDO:0024659	colorectal Kaposi sarcoma
MONDO:0012681	febrile seizures, familial, 7
MONDO:0012682	susceptibility to infection due to TYK2 deficiency
MONDO:0010020	congenital generalized lipodystrophy type 2
MONDO:0012680	nephronophthisis 7
MONDO:0024652	embryonic cyst of fallopian tube
MONDO:0024651	corticosteroid-induced osteoporosis
MONDO:0024654	skull disorder
MONDO:0024653	skull neoplasm
MONDO:0024656	colorectal lymphoma
MONDO:0024655	rheumatic pericarditis
MONDO:0024658	extrahepatic bile duct sarcoma
MONDO:0024657	macrocystic neurilemmoma
MONDO:0010008	sarcosinemia
MONDO:0010007	microbrachycephaly-ptosis-cleft lip syndrome
MONDO:0009039	Baller-Gerold syndrome
MONDO:0012669	Legius syndrome
MONDO:0009038	craniosynostosis-fibular aplasia syndrome
MONDO:0010009	SC phocomelia syndrome
MONDO:0009037	craniosynostosis with anomalies of the cranial base and digits
MONDO:0009036	cardiocranial syndrome, Pfeiffer type
MONDO:0009035	craniometaphyseal dysplasia, autosomal recessive
MONDO:0024650	drug-induced osteoporosis
MONDO:0009034	craniofacial dyssynostosis
MONDO:0012674	age related macular degeneration 10
MONDO:0009033	temtamy syndrome
MONDO:0010011	schizencephaly
MONDO:0009032	cranioectodermal dysplasia
MONDO:0010010	Schinzel-Giedion syndrome
MONDO:0012675	corticosteroid-binding globulin deficiency
MONDO:0010013	schneckenbecken dysplasia
MONDO:0012672	cholelithiasis
MONDO:0009031	craniodiaphyseal dysplasia
MONDO:0010012	autoimmune polyendocrinopathy type 2
MONDO:0012673	colorectal cancer, susceptibility to, 2
MONDO:0009030	cranial nerves, recurrent paresis of
MONDO:0010015	anterior segment dysgenesis 7
MONDO:0012678	atrial fibrillation, familial, 5
MONDO:0010014	craniometadiaphyseal dysplasia, wormian bone type
MONDO:0012679	autosomal recessive osteopetrosis 6
MONDO:0012676	autosomal recessive osteopetrosis 4
MONDO:0010017	sea-blue histiocyte syndrome
MONDO:0012677	atrial fibrillation, familial, 4
MONDO:0010016	sclerosteosis 1
MONDO:0024649	optic tract astrocytoma
MONDO:0024648	optic tract meningioma
MONDO:0012670	autosomal recessive nonsyndromic deafness 63
MONDO:0012671	tremor, hereditary essential, 3
MONDO:0000601	autoimmune disease of urogenital tract
MONDO:0000600	nosophobia
MONDO:0000630	immune system organ benign neoplasm
MONDO:0000634	thoracic benign neoplasm
MONDO:0000633	sensory organ benign neoplasm
MONDO:0000632	uterine benign neoplasm
MONDO:0000631	bone benign neoplasm
MONDO:0012616	MRT8
MONDO:0012617	intellectual disability, autosomal recessive 9
MONDO:0012614	intellectual disability, autosomal recessive 6
MONDO:0012615	intellectual disability, autosomal recessive 7
MONDO:0012618	intellectual disability, autosomal recessive 10
MONDO:0012619	intellectual disability, autosomal recessive 11
MONDO:0012620	prostate cancer, hereditary, 10
MONDO:0012623	intellectual disability, autosomal recessive 4
MONDO:0012624	acyl-CoA dehydrogenase 9 deficiency
MONDO:0012621	deafness-infertility syndrome
MONDO:0012622	leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome
MONDO:0000627	benign endocrine neoplasm
MONDO:0000626	vestibular gland benign neoplasm
MONDO:0000625	benign male reproductive system neoplasm
MONDO:0000624	benign female reproductive system neoplasm
MONDO:0000629	cardiovascular organ benign neoplasm
MONDO:0000628	central nervous system organ benign neoplasm
MONDO:0000641	cerebellar medulloblastoma
MONDO:0000640	central nervous system primitive neuroectodermal neoplasm
MONDO:0000645	fallopian tube benign neoplasm
MONDO:0000644	cervical benign neoplasm
MONDO:0000643	vulvar benign neoplasm
MONDO:0000642	brain meningioma
MONDO:0012605	isolated microphthalmia 5
MONDO:0012606	mycobacterium tuberculosis, susceptibility to, 2
MONDO:0012603	episodic kinesigenic dyskinesia 2
MONDO:0012604	isolated microphthalmia 3
MONDO:0012609	Alzheimer disease 12
MONDO:0012607	asthma-related traits, susceptibility to, 5
MONDO:0012608	autosomal recessive lower motor neuron disease with childhood onset
MONDO:0012612	intellectual disability, autosomal recessive 12
MONDO:0012613	intellectual disability, autosomal recessive 5
MONDO:0012610	inflammatory bowel disease 10
MONDO:0012611	polyhydramnios, megalencephaly, and symptomatic epilepsy
MONDO:0000638	benign glioma
MONDO:0000637	musculoskeletal system cancer
MONDO:0000636	musculoskeletal system benign neoplasm
MONDO:0000635	osteoblastoma
MONDO:0000639	cartilage cancer
MONDO:0000612	lymphatic system cancer
MONDO:0000611	pre-malignant neoplasm
MONDO:0000610	marantic endocarditis
MONDO:0012601	autism, susceptibility to, 10
MONDO:0012602	autosomal recessive nonsyndromic deafness 24
MONDO:0012600	autism, susceptibility to, 9
MONDO:0000605	hypersensitivity reaction disease
MONDO:0000604	autonomic peripheral neuropathy
MONDO:0000603	autoimmune disease of cardiovascular system
MONDO:0000602	autoimmune disease of blood
MONDO:0000609	sideroblastic anemia with spinocerebellar ataxia
MONDO:0000608	familial juvenile hyperuricemic nephropathy
MONDO:0000607	primary cutaneous T-cell non-Hodgkin lymphoma
MONDO:0000606	gluten allergy
MONDO:0000623	organ system benign neoplasm
MONDO:0000622	cell type benign neoplasm
MONDO:0000621	immune system cancer
MONDO:0000620	breast benign neoplasm
MONDO:0000616	progesterone-receptor negative breast cancer
MONDO:0000615	progesterone-receptor positive breast cancer
MONDO:0000614	estrogen-receptor negative breast cancer
MONDO:0000613	estrogen-receptor positive breast cancer
MONDO:0000619	triple-receptor negative breast cancer
MONDO:0000618	Her2-receptor negative breast cancer
MONDO:0000617	Her2-receptor positive breast cancer
MONDO:0034099	SYNGAP1-related developmental and epileptic encephalopathy
MONDO:0034092	optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome
MONDO:0022067	Cantu sanchez-corona fragoso syndrome
MONDO:0022060	calloso-genital dysplasia
MONDO:0009089	deafness-oligodontia syndrome
MONDO:0010088	mucosulfatidosis
MONDO:0009088	deafness, neural, with atypical atopic dermatitis
MONDO:0010087	Sugarman brachydactyly
MONDO:0009087	deafness, neural, congenital moderate
MONDO:0034054	severe combined immunodeficiency due to CD70 deficiency
MONDO:0009086	deafness-small bowel diverticulosis-neuropathy syndrome
MONDO:0010089	isolated sulfite oxidase deficiency
MONDO:0009085	deafness-vitiligo-achalasia syndrome
MONDO:0009084	conductive deafness-ptosis-skeletal anomalies syndrome
MONDO:0009083	conductive deafness-malformed external ear syndrome
MONDO:0009082	high myopia-sensorineural deafness syndrome
MONDO:0009081	deafness, congenital, with total albinism
MONDO:0009080	split hand-foot malformation 1 with sensorineural hearing loss
MONDO:0010080	familial infantile bilateral striatal necrosis
MONDO:0010082	subaortic stenosis-short stature syndrome
MONDO:0010081	subaortic stenosis, membranous
MONDO:0010084	sucrosuria, hiatus hernia and intellectual disability
MONDO:0010083	succinic semialdehyde dehydrogenase deficiency
MONDO:0010086	sudden infant death syndrome
MONDO:0010085	Schilder disease
MONDO:0022055	Calabro syndrome
MONDO:0022057	calcifying epithelial odontogenic tumor
MONDO:0010077	spondyloepimetaphyseal dysplasia-short limb-abnormal calcification syndrome
MONDO:0009099	nephrogenic diabetes insipidus-intracranial calcification syndrome
MONDO:0010076	spondyloepimetaphyseal dysplasia, Irapa type
MONDO:0009098	dextrocardia with unusual facies and microphthalmia
MONDO:0009097	persistent hyperplastic primary vitreous, autosomal recessive
MONDO:0010079	Canavan disease
MONDO:0009096	hereditary diffuse leukoencephalopathy with axonal spheroids and pigmented glia
MONDO:0010078	spondyloperipheral dysplasia-short ulna syndrome
MONDO:0009095	dermatoosteolysis, Kirghizian type
MONDO:0009094	dermochondrocorneal dystrophy
MONDO:0009093	dermatoleukodystrophy
MONDO:0009092	polycystic lipomembranous osteodysplasia with sclerosing leukoencephaly
MONDO:0009091	non-acquired combined pituitary hormone deficiency with spine abnormalities
MONDO:0009090	deafness, sensorineural, autosomal-mitochondrial type
MONDO:0010071	spondyloenchondrodysplasia
MONDO:0010070	brachyolmia type 1, Hobaek type
MONDO:0010073	spondyloepiphyseal dysplasia tarda, Kohn type
MONDO:0010072	spondyloepiphyseal dysplasia tarda, autosomal recessive
MONDO:0010075	spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures
MONDO:0010074	brachyolmia type 1, toledo type
MONDO:0009069	congenital lactic acidosis, Saguenay-Lac-Saint-Jean type
MONDO:0009068	cytochrome-c oxidase deficiency disease
MONDO:0009067	cystinuria
MONDO:0009066	juvenile nephropathic cystinosis
MONDO:0010066	familial isolated congenital asplenia
MONDO:0010065	spinocerebellar degeneration with slow eye movements
MONDO:0009065	cystinosis, nephropathic
MONDO:0010068	spondyloepimetaphyseal dysplasia, sponastrime type
MONDO:0009064	ocular cystinosis
MONDO:0010067	splenoportal vascular anomalies
MONDO:0009063	ventriculomegaly-cystic kidney disease
MONDO:0009062	cystic fibrosis-gastritis-megaloblastic anemia syndrome
MONDO:0009061	cystic fibrosis
MONDO:0010069	spondylocostal dysostosis-anal and genitourinary malformations syndrome
MONDO:0009060	cystic disease of lung
MONDO:0010060	infantile onset spinocerebellar ataxia
MONDO:0010062	spinocerebellar ataxia-dysmorphism syndrome
MONDO:0010061	autosomal recessive cerebellar ataxia-blindness-deafness syndrome
MONDO:0010064	spastic ataxia-corneal dystrophy syndrome
MONDO:0010063	corneal-cerebellar syndrome
MONDO:0022034	lentivirus infection
MONDO:0022037	large-cell immunoblastic lymphoma
MONDO:0009079	DOORS syndrome
MONDO:0009078	Jervell and Lange-Nielsen syndrome
MONDO:0009077	deafness, congenital, and familial myoclonic epilepsy
MONDO:0010055	spinal muscular atrophy with microcephaly and mental subnormality
MONDO:0009076	autosomal recessive nonsyndromic deafness 1A
MONDO:0010054	spinal muscular atrophy with intellectual disability
MONDO:0009075	Dandy-Walker malformation-postaxial polydactyly syndrome
MONDO:0010057	spinal muscular atrophy, Ryukyuan type
MONDO:0010056	spinal muscular atrophy, type IV
MONDO:0009074	facial dysmorphism-macrocephaly-myopia-Dandy-Walker malformation syndrome
MONDO:0009073	Ritscher-Schinzel syndrome 1
MONDO:0010059	spinal muscular atrophy, type I, with congenital bone fractures
MONDO:0009072	Dandy-Walker syndrome
MONDO:0010058	scapuloperoneal spinal muscular atrophy, autosomal recessive
MONDO:0009071	hereditary renal hypouricemia
MONDO:0034082	necrobiosis lipoidica
MONDO:0009070	D-glyceric aciduria
MONDO:0010051	spastic tetraplegia-retinitis pigmentosa-intellectual disability syndrome
MONDO:0010050	spastic pseudosclerosis
MONDO:0010053	hereditary spherocytosis type 3
MONDO:0010052	spermatogenic failure 4
MONDO:0022094	Cartwright Nelson Fryns syndrome
MONDO:0022096	pyogenic granuloma
MONDO:0022098	catamenial pneumothorax
MONDO:0034022	Bethlem myopathy 2
MONDO:0034021	spondylodysplastic Ehlers-Danlos syndrome
MONDO:0036688	rhabdomyoma
MONDO:0034024	kyphoscoliotic Ehlers-Danlos syndrome
MONDO:0022089	Carnevale hernandez castillo syndrome
MONDO:0036696	spleen neoplasm
MONDO:0022070	Cantu sanchez-corona hernandez syndrome
MONDO:0022071	carbon baby syndrome
MONDO:0010099	Tay-Sachs disease AB variant
MONDO:0010098	taurodontism
MONDO:0034041	congenital axonal neuropathy with encephalopathy
MONDO:0010091	Cold-induced sweating syndrome 1
MONDO:0010090	Summitt syndrome
MONDO:0010093	syndesmodysplasic dwarfism
MONDO:0010092	Filippi syndrome
MONDO:0010095	ataxia-tapetoretinal degeneration syndrome
MONDO:0010094	spondylocarpotarsal synostosis syndrome
MONDO:0010097	Tatsumi factor deficiency
MONDO:0010096	tardive dyskinesia
MONDO:0024520	renal hypodysplasia/aplasia 3
MONDO:0000553	uterine corpus endometrial carcinoma
MONDO:0000552	breast lobular carcinoma
MONDO:0024522	amyloidosis, primary localized cutaneous, 1
MONDO:0000551	retroperitoneal neuroblastoma
MONDO:0000550	extra-adrenal sympathetic paraganglioma
MONDO:0024521	aortic aneurysm, familial abdominal, 1
MONDO:0024524	dyschromatosis universalis hereditaria 1
MONDO:0000557	hereditary ataxia
MONDO:0024523	aortic valve disease 1
MONDO:0000556	autosomal recessive cerebellar ataxia
MONDO:0024526	Zimmermann-Laband syndrome 1
MONDO:0000555	autosomal recessive hypophosphatemic rickets
MONDO:0024525	Fanconi renotubular syndrome 1
MONDO:0000554	endocervical adenocarcinoma
MONDO:0012539	Joubert syndrome 6
MONDO:0012537	split-hand/foot malformation with long bone deficiency 2
MONDO:0012538	nemaline myopathy 7
MONDO:0012542	psoriasis 8, susceptibility to
MONDO:0012543	optic atrophy 5
MONDO:0036511	childhood malignant kidney neoplasm
MONDO:0012540	age related macular degeneration 4
MONDO:0012541	deafness with labyrinthine aplasia, microtia, and microdontia
MONDO:0012546	nephrotic syndrome, type 3
MONDO:0012547	Noonan syndrome 4
MONDO:0012544	brachydactyly-syndactyly syndrome
MONDO:0012545	neutral lipid storage myopathy
MONDO:0024517	schwannomatosis 1
MONDO:0024516	familial acne inversa
MONDO:0000549	cervical neuroblastoma
MONDO:0024519	renal hypodysplasia/aplasia 1
MONDO:0000548	ovarian clear cell cancer
MONDO:0024518	reactive thrombocytosis
MONDO:0000547	ovarian serous carcinoma
MONDO:0000564	cerebellar ataxia, mental retardation and dysequlibrium syndrome
MONDO:0000563	GRID2-related autosomal dominant spinocerebellar ataxia
MONDO:0000562	hypomyelinating leukoencephalopathy
MONDO:0000561	spinocerebellar ataxia type 16
MONDO:0000568	autoimmune disease of central nervous system
MONDO:0024512	spondyloarthropathy, susceptibility to
MONDO:0000567	C1 inhibitor deficiency
MONDO:0000566	substance withdrawal disorder
MONDO:0000565	infective endocarditis
MONDO:0012528	hypogonadotropic hypogonadism 4 with or without anosmia
MONDO:0012529	Diamond-Blackfan anemia 3
MONDO:0012526	hereditary angioedema type 3
MONDO:0012527	cataract 11 multiple types
MONDO:0000560	spinocerebellar ataxia type 4
MONDO:0012531	xeroderma pigmentosum group B
MONDO:0012532	hereditary hemorrhagic telangiectasia type 4
MONDO:0012530	palmoplantar keratoderma-XX sex reversal-predisposition to squamous cell carcinoma syndrome
MONDO:0012535	holoprosencephaly, recurrent infections, and monocytosis
MONDO:0012536	osteogenesis imperfecta type 7
MONDO:0012533	autism, susceptibility to, 7
MONDO:0012534	combined oxidative phosphorylation defect type 4
MONDO:0024506	Adams-Oliver syndrome 1
MONDO:0024505	disorder by anatomical region
MONDO:0024508	epilepsy, hot water, 1
MONDO:0000558	spastic ataxia
MONDO:0024507	aniridia 1
MONDO:0000531	bronchus mucoepidermoid carcinoma
MONDO:0000530	rectum adenoma
MONDO:0024500	duodenal neuroendocrine neoplasm
MONDO:0024502	gallbladder neuroendocrine neoplasm
MONDO:0000535	tonsil squamous cell carcinoma
MONDO:0024501	appendix neuroendocrine neoplasm
MONDO:0000534	trachea mucoepidermoid carcinoma
MONDO:0024504	enterochromaffin cell serotonin-producing pancreatic neuroendocrine tumor
MONDO:0000533	vaginal carcinoma
MONDO:0024503	digestive system neuroendocrine neoplasm
MONDO:0000532	lung combined type small cell adenocarcinoma
MONDO:0012517	atypical Gaucher disease due to saposin C deficiency
MONDO:0012518	congenital myasthenic syndrome 12
MONDO:0012515	glaucoma 1, open angle, M
MONDO:0012516	mandibulofacial dysostosis-microcephaly syndrome
MONDO:0012519	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion
MONDO:0012520	insulin-resistance syndrome type A
MONDO:0012521	herpes simplex encephalitis
MONDO:0012524	corticosterone methyloxidase type 2 deficiency
MONDO:0012525	Leber congenital amaurosis 12
MONDO:0012522	diabetes mellitus, transient neonatal, 3
MONDO:0012523	retinitis pigmentosa 36
MONDO:0000527	colon adenoma
MONDO:0000526	appendix carcinoid tumor
MONDO:0000525	cecum villous adenoma
MONDO:0000542	duodenum adenoma
MONDO:0000541	jejunal adenocarcinoma
MONDO:0000540	small intestinal neuroendocrine tumor G1
MONDO:0000546	parotid gland adenoid cystic carcinoma
MONDO:0000545	sublingual gland adenoid cystic carcinoma
MONDO:0000544	mucosal melanoma
MONDO:0000543	ovarian melanoma
MONDO:0012506	arrhythmogenic right ventricular dysplasia 11
MONDO:0012507	retinal cone dystrophy 4
MONDO:0012504	camptodactyly-tall stature-scoliosis-hearing loss syndrome
MONDO:0012505	pigmented nodular adrenocortical disease, primary, 2
MONDO:0012508	agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome
MONDO:0012509	pigmented nodular adrenocortical disease, primary, 1
MONDO:0012510	combined oxidative phosphorylation defect type 2
MONDO:0012513	maturity-onset diabetes of the young type 7
MONDO:0012514	hypomyelinating leukodystrophy 5
MONDO:0012511	preterm premature rupture of the membranes
MONDO:0012512	fatal mitochondrial disease due to combined oxidative phosphorylation defect type 3
MONDO:0000539	striated muscle rhabdoid tumor
MONDO:0000538	spindle epithelial tumor with thymus-like differentiation tumor
MONDO:0000537	gastrointestinal carcinoma
MONDO:0000536	pharyngeal squamous cell carcinoma
MONDO:0000597	Munchausen by proxy
MONDO:0024564	cerebroretinal microangiopathy with calcifications and cysts 1
MONDO:0024563	herpes simplex encephalitis, susceptibility to, 1
MONDO:0000596	paraphilic disorder
MONDO:0000595	sexual and gender identity disorders
MONDO:0024566	febrile seizures, familial, 11
MONDO:0000594	pervasive developmental disorder
MONDO:0024565	ectodermal dysplasia-syndactyly syndrome 1
MONDO:0024568	infantile liver failure syndrome 1
MONDO:0024567	hypotonia, infantile, with psychomotor retardation and characteristic facies 1
MONDO:0000599	writing disorder
MONDO:0000598	aphasia
MONDO:0024569	optic atrophy 8
MONDO:0024560	PDA1
MONDO:0000593	autoimmune disease of skin and connective tissue
MONDO:0000592	specific developmental disorder
MONDO:0024562	sick sinus syndrome 1
MONDO:0000591	intrinsic cardiomyopathy
MONDO:0024561	vitelliform macular dystrophy 3
MONDO:0000590	autoimmune disease of peripheral nervous system
MONDO:0012586	coronary artery disease, autosomal dominant 2
MONDO:0012587	hypertension, essential, susceptibility to, 7
MONDO:0012584	systemic lupus erythematosus, susceptibility to, 9
MONDO:0012585	coronary heart disease, susceptibility to, 7
MONDO:0012588	neuronal ceroid lipofuscinosis 7
MONDO:0012589	Pitt-Hopkins syndrome
MONDO:0012582	interstitial lung disease due to ABCA3 deficiency
MONDO:0012583	tooth agenesis, selective, 5
MONDO:0012580	hereditary pulmonary alveolar proteinosis
MONDO:0012581	osteogenesis imperfecta type 8
MONDO:0024553	myopathy, lactic acidosis, and sideroblastic anemia 1
MONDO:0024552	linear skin defects with multiple congenital anomalies 1
MONDO:0024555	megalencephalic leukoencephalopathy with subcortical cysts 1
MONDO:0024554	D-2-hydroxyglutaric aciduria 1
MONDO:0024557	ataxia-telangiectasia-like disorder 1
MONDO:0024556	epilepsy, familial focal, with variable foci 1
MONDO:0024559	AAT1
MONDO:0024558	radioulnar synostosis with amegakaryocytic thrombocytopenia 1
MONDO:0024551	X-linked lymphoproliferative disease due to SH2D1A deficiency
MONDO:0024550	frontometaphyseal dysplasia 1
MONDO:0012575	branchiootorenal syndrome 2
MONDO:0012576	supranuclear palsy, progressive, 3
MONDO:0012573	vesicoureteral reflux 2
MONDO:0012574	Potocki-Lupski syndrome
MONDO:0012579	autoimmune pulmonary alveolar proteinosis
MONDO:0012577	asthma-related traits, susceptibility to, 4
MONDO:0012578	autism, susceptibility to, 13
MONDO:0024549	microphthalmia with coloboma 1
MONDO:0012571	primary ciliary dyskinesia 6
MONDO:0012572	Sakoda complex
MONDO:0012570	body skin hyperlaxity due to vitamin K-dependent coagulation factor deficiency
MONDO:0024542	cerebellar ataxia, intellectual disability, and dysequilibrium syndrome 1
MONDO:0024541	trichohepatoenteric syndrome 1
MONDO:0000574	CD45 deficiency
MONDO:0024544	Heimler syndrome 1
MONDO:0000573	recombinase activating gene 2 deficiency
MONDO:0024543	brittle cornea syndrome 1
MONDO:0000572	recombinase activating gene 1 deficiency
MONDO:0024546	hypertrophic osteoarthropathy, primary, autosomal recessive, 1
MONDO:0000579	coronin-1A deficiency
MONDO:0024545	Miyoshi muscular dystrophy 1
MONDO:0000578	CD3gamma deficiency
MONDO:0024548	peeling skin syndrome 1
MONDO:0000577	congenital anemia
MONDO:0024547	pancreatic agenesis 1
MONDO:0000576	CD3delta deficiency
MONDO:0012559	primary immunodeficiency syndrome due to p14 deficiency
MONDO:0000571	CD3zeta deficiency
MONDO:0000570	severe combined immunodeficiency due to artemis deficiency
MONDO:0024540	Jervell and Lange-Nielsen syndrome 1
MONDO:0012564	Polyosteolysis-hyperostosis syndrome
MONDO:0012565	Fanconi anemia complementation group N
MONDO:0012562	holoprosencephaly 7
MONDO:0012563	holoprosencephaly 9
MONDO:0012568	osteoarthritis susceptibility 4
MONDO:0012569	mitral valve prolapse, myxomatous 3
MONDO:0012566	autism, susceptibility to, 11
MONDO:0012567	autism, susceptibility to, 12
MONDO:0024539	choroidal dystrophy, central areolar, 1
MONDO:0024538	basal ganglia calcification, idiopathic, 1
MONDO:0000569	autoimmune disease of endocrine system
MONDO:0012560	invasive pneumococcal disease, recurrent isolated, 1
MONDO:0012561	congenital anomalies of kidney and urinary tract 1
MONDO:0000586	autoimmune disease of exocrine system
MONDO:0024531	myopathy, tubular aggregate, 1
MONDO:0024530	Bethlem myopathy 1
MONDO:0000585	Good syndrome
MONDO:0024533	pulmonary hypertension, primary, 1
MONDO:0000584	B cell linker protein deficiency
MONDO:0024532	otofaciocervical syndrome 1
MONDO:0000583	immunoglobulin beta deficiency
MONDO:0024535	Singleton-Merten syndrome 1
MONDO:0024534	Dowling-Degos disease 1
MONDO:0000589	autoimmune disease of musculoskeletal system
MONDO:0024537	Brown-Vialetto-van Laere syndrome 1
MONDO:0000588	autoimmune disease of gastrointestinal tract
MONDO:0024536	glucocorticoid deficiency 1
MONDO:0000587	autoimmune disease of ear, nose and throat
MONDO:0012548	Kostmann syndrome
MONDO:0012549	autosomal recessive ataxia, Beauce type
MONDO:0000582	immunoglobulin alpha deficiency
MONDO:0000581	lambda 5 deficiency
MONDO:0000580	CD40 ligand deficiency
MONDO:0012553	cerebrooculofacioskeletal syndrome 2
MONDO:0012554	cerebrooculofacioskeletal syndrome 4
MONDO:0012551	alopecia areata 2
MONDO:0012552	multiple endocrine neoplasia type 4
MONDO:0036501	refractory malignant neoplasm
MONDO:0012557	cardiomyopathy-hypotonia-lactic acidosis syndrome
MONDO:0012558	epiphyseal dysplasia, Baumann type
MONDO:0012555	Cornelia de Lange syndrome 3
MONDO:0012556	DK1-CDG
MONDO:0024528	progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1
MONDO:0024527	glomerulopathy with fibronectin deposits 1
MONDO:0024529	MVP1
MONDO:0012550	iris pattern
MONDO:0000513	bone ameloblastoma
MONDO:0000512	ameloblastoma
MONDO:0000511	gallbladder adenoma
MONDO:0000510	synucleinopathy
MONDO:0012502	normophosphatemic familial tumoral calcinosis
MONDO:0012503	thiopurine S-methyltransferase deficiency
MONDO:0012500	chilblain lupus 1
MONDO:0012501	mutagen sensitivity
MONDO:0000506	Caroli disease
MONDO:0000505	small cell neuroendocrine carcinoma
MONDO:0000504	follicular lymphoma
MONDO:0000503	lung adenocarcinoma in situ
MONDO:0000509	non-syndromic intellectual disability
MONDO:0000508	syndromic intellectual disability
MONDO:0000507	inclusion body myopathy with Paget disease of bone and frontotemporal dementia
MONDO:0000520	parietal lobe ependymal tumor
MONDO:0000524	mixed extragonadal germ cell cancer
MONDO:0000523	conjunctival nevus
MONDO:0000522	inflammatory myofibroblastic tumor
MONDO:0000521	salivary gland carcinoma
MONDO:0000517	brain stem medulloblastoma
MONDO:0000516	phalanx chondroma
MONDO:0000515	bone chondrosarcoma
MONDO:0000514	bone squamous cell carcinoma
MONDO:0000519	corpus callosum oligodendroglioma
MONDO:0000518	sacrum chordoma
MONDO:0000502	villous adenoma
MONDO:0000501	Jensen syndrome
MONDO:0000500	tongue squamous cell carcinoma
MONDO:0036591	adrenal cortex neoplasm
MONDO:0036595	ovarian Sertoli-Leydig cell tumor
MONDO:0024597	CD3epsilon deficiency
MONDO:0024582	male reproductive system neoplasm
MONDO:0024583	hernia
MONDO:0024575	pregnancy disorder
MONDO:0024574	von Willebrand disease (hereditary or acquired)
MONDO:0024571	AIDS-related disorder
MONDO:0024570	hyperparathyroidism 4
MONDO:0024573	familial hypertrophic cardiomyopathy
MONDO:0024572	immunodeficiency-related disorder
MONDO:0012597	prostate cancer, hereditary, 9
MONDO:0012598	fibromatosis, gingival, 4
MONDO:0012595	leprosy, susceptibility to, 4
MONDO:0012596	PSAT deficiency
MONDO:0012599	hypertension, essential, susceptibility to, 8
MONDO:0012590	XFE progeroid syndrome
MONDO:0012593	brain-lung-thyroid syndrome
MONDO:0012594	complement factor I deficiency
MONDO:0012591	osteogenesis imperfecta type 5
MONDO:0012592	osteogenesis imperfecta type 11
MONDO:0000432	lymphoplasmacytic lymphoma
MONDO:0000431	mantle cell lymphoma
MONDO:0000430	mature T-cell and NK-cell non-Hodgkin lymphoma
MONDO:0000436	T-cell large granular lymphocyte leukemia
MONDO:0000435	splenic marginal zone lymphoma
MONDO:0000434	peripheral T-cell lymphoma
MONDO:0024404	meningitis caused by anaerobic bacteria
MONDO:0000433	marginal zone B-cell lymphoma
MONDO:0012418	autosomal recessive nonsyndromic deafness 62
MONDO:0012419	age related macular degeneration 7
MONDO:0012416	Devriendt syndrome
MONDO:0012417	heart-hand syndrome, Slovenian type
MONDO:0012421	autosomal recessive nonsyndromic deafness 44
MONDO:0012422	type 1 diabetes mellitus 19
MONDO:0012420	autosomal recessive nonsyndromic deafness 49
MONDO:0012425	corneal dystrophy, fuchs endothelial, 2
MONDO:0012426	immunodeficiency 25
MONDO:0012423	MORM syndrome
MONDO:0012424	heat-shock RNA 1
MONDO:0000429	autosomal genetic disease
MONDO:0000428	Y-linked disease
MONDO:0000427	autosomal recessive disease
MONDO:0000426	autosomal dominant disease
MONDO:0000443	adenylosuccinase lyase deficiency
MONDO:0000442	paramyloidosis
MONDO:0000441	X-linked myopathy with excessive autophagy
MONDO:0000440	metabolic acidosis
MONDO:0000447	autosomal dominant polycystic liver disease
MONDO:0000446	midface dysplasia
MONDO:0000445	neuroacanthocytosis
MONDO:0000444	ARC syndrome
MONDO:0012407	pyridoxal phosphate-responsive seizures
MONDO:0012408	microphthalmia, isolated, with coloboma 3
MONDO:0012405	polyposis syndrome, hereditary mixed, 2
MONDO:0012406	hyperparathyroidism 3
MONDO:0012409	isolated microphthalmia 2
MONDO:0012410	Finnish upper limb-onset distal myopathy
MONDO:0012411	giant axonal neuropathy 2
MONDO:0012414	neuronal ceroid lipofuscinosis 10
MONDO:0012415	progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 4
MONDO:0012412	complement component 7 deficiency
MONDO:0012413	syndromic microphthalmia type 5
MONDO:0000439	batten disease
MONDO:0000438	ataxia with oculomotor apraxia type 2
MONDO:0000437	cerebellar ataxia
MONDO:0000410	funisitis
MONDO:0000414	childhood electroclinical syndrome
MONDO:0000413	infancy electroclinical syndrome
MONDO:0000412	neonatal period electroclinical syndrome
MONDO:0000411	electroclinical syndrome
MONDO:0012400	cortical dysplasia-focal epilepsy syndrome
MONDO:0012403	systemic lupus erythematosus, susceptibility to, 7
MONDO:0012404	systemic lupus erythematosus, susceptibility to, 8
MONDO:0012401	congenital stromal corneal dystrophy
MONDO:0012402	opioid dependence, susceptibility to, 1
MONDO:0000407	malignant pleural solitary fibrous tumor
MONDO:0000406	Brown-Vialetto-van Laere syndrome
MONDO:0000405	anal canal cancer
MONDO:0000404	cell type cancer
MONDO:0000409	chorioamnionitis
MONDO:0000408	fetal alcohol spectrum disorder
MONDO:0000421	inborn serine deficiency
MONDO:0000420	cerebral folate receptor alpha deficiency
MONDO:0000425	X-linked disease
MONDO:0000424	inborn vitamin B12 deficiency
MONDO:0000423	coenzyme Q10 deficiency disease
MONDO:0000422	inborn glycogen metabolism disorder
MONDO:0000418	Ohtahara syndrome
MONDO:0000417	early onset absence epilepsy
MONDO:0000416	variable age at onset electroclinical syndrome
MONDO:0000415	adolescence-adult electroclinical syndrome
MONDO:0000419	3-Methylcrotonyl-CoA carboxylase deficiency
MONDO:0000476	generalized dystonia
MONDO:0000475	pyrimidine metabolic disorder
MONDO:0000474	pericardium disease
MONDO:0000473	arterial disorder
MONDO:0000479	segmental dystonia
MONDO:0000478	multifocal dystonia
MONDO:0000477	focal dystonia
MONDO:0000472	rheumatic heart disease
MONDO:0000471	tricuspid valve disease
MONDO:0000470	endocardium disease
MONDO:0012465	hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency
MONDO:0012466	Parkinson disease 13, autosomal dominant, susceptibility to
MONDO:0012463	retinitis pigmentosa 35
MONDO:0012464	cone-rod dystrophy 10
MONDO:0012469	myopia 14
MONDO:0012467	cold-induced sweating syndrome 2
MONDO:0012468	rhizomelic dysplasia, scoliosis, and retinitis pigmentosa
MONDO:0012461	bulimia nervosa, susceptibility to, 2
MONDO:0012462	autosomal recessive frontotemporal pachygyria
MONDO:0012460	autosomal recessive nonsyndromic deafness 67
MONDO:0000487	hemidystonia
MONDO:0024432	nerve plexus disease
MONDO:0000486	craniofacial dystonia
MONDO:0024431	bilirubin metabolism disease
MONDO:0000485	spasmodic dystonia
MONDO:0000484	oromandibular dystonia
MONDO:0000489	diabetic encephalopathy
MONDO:0000488	periampullary adenoma
MONDO:0012449	spinocerebellar ataxia type 23
MONDO:0000483	oculogyric crisis
MONDO:0000482	focal hand dystonia
MONDO:0000481	cervical dystonia
MONDO:0024430	allesthesia
MONDO:0000480	anismus
MONDO:0012454	alcohol sensitivity, acute
MONDO:0012455	Kleefstra syndrome
MONDO:0012452	autosomal recessive nonsyndromic deafness 65
MONDO:0012453	hereditary spastic paraplegia 31
MONDO:0012458	hypertension, essential, susceptibility to, 5
MONDO:0012459	hypertension, essential, susceptibility to, 6
MONDO:0012456	congenital primary aphakia
MONDO:0012457	pyloric stenosis, infantile hypertrophic, 2
MONDO:0024429	Alice in wonderland syndrome
MONDO:0012450	spinocerebellar ataxia type 28
MONDO:0012451	esophagitis, eosinophilic, 1
MONDO:0024421	short stature contractures hypotonia
MONDO:0000454	multiple synostoses syndrome
MONDO:0000453	short QT syndrome
MONDO:0000452	progressive relapsing multiple sclerosis
MONDO:0024422	auditory perceptual disorders
MONDO:0000451	primary progressive multiple sclerosis
MONDO:0000458	proneural glioblastoma
MONDO:0000457	classical glioblastoma
MONDO:0000456	cerebral creatine deficiency syndrome
MONDO:0000455	cone dystrophy
MONDO:0012438	pontocerebellar hypoplasia type 5
MONDO:0012439	Alagille syndrome due to a NOTCH2 point mutation
MONDO:0000450	secondary progressive multiple sclerosis
MONDO:0012443	aneurysm, intracranial berry, 4
MONDO:0012444	neurodegeneration with brain iron accumulation 2B
MONDO:0012441	migraine with or without aura, susceptibility to, 11
MONDO:0012442	autosomal recessive nonsyndromic deafness 66
MONDO:0012447	synpolydactyly type 3
MONDO:0012448	hereditary spastic paraplegia 33
MONDO:0012445	autosomal recessive nonsyndromic deafness 59
MONDO:0012446	seborrhea-like dermatitis with psoriasiform elements
MONDO:0024418	muscular fibrosis multifocal obstructed vessels
MONDO:0024417	perceptual disorders
MONDO:0000449	Opitz-GBBB syndrome
MONDO:0024419	enthesitis
MONDO:0000448	paraganglioma
MONDO:0012440	migraine with or without aura, susceptibility to, 10
MONDO:0000465	atrioventricular block
MONDO:0024410	infection caused by Bifidobacterium
MONDO:0000464	Stargardt disease
MONDO:0000463	Ochoa syndrome
MONDO:0024412	Peptostreptococcus infectious disease
MONDO:0000462	eye adnexa disease
MONDO:0000469	sinoatrial node disease
MONDO:0024414	anaerobic cellulitis
MONDO:0000468	third-degree atrioventricular block
MONDO:0000467	second-degree atrioventricular block
MONDO:0024416	Neorickettsia infectious disease
MONDO:0000466	first-degree atrioventricular block
MONDO:0024415	hemorrhagic duodenitis
MONDO:0012429	Aicardi-Goutieres syndrome 2
MONDO:0012427	Loeys-Dietz syndrome 2
MONDO:0012428	kyphoscoliosis 1
MONDO:0000461	nutritional biotin deficiency
MONDO:0000460	neural glioblastoma
MONDO:0012432	Joubert syndrome 5
MONDO:0012433	Senior-Loken syndrome 6
MONDO:0012430	cerebellar ataxia, intellectual disability, and dysequilibrium syndrome 2
MONDO:0012431	diaphragmatic hernia 3
MONDO:0012436	neonatal diabetes mellitus with congenital hypothyroidism
MONDO:0012437	cataract 21 multiple types
MONDO:0012434	arrhythmogenic right ventricular dysplasia 10
MONDO:0012435	3-methylglutaconic aciduria type 5
MONDO:0000459	mesenchymal glioblastoma
MONDO:0000403	organ system cancer
MONDO:0000402	small cell carcinoma
MONDO:0000401	congenital bile acid synthesis defect
MONDO:0000400	mixed cerebral palsy
MONDO:0024487	nail infection
MONDO:0024486	familial chronic mucocutaneous candidiasis
MONDO:0024489	general tumor grading characteristic
MONDO:0024488	tumor grading characteristic
MONDO:0024481	skin appendage disease
MONDO:0024480	dermatosis of eyelid
MONDO:0024483	urothelial hyperplasia
MONDO:0024482	eccrine sweat gland hamartoma
MONDO:0024485	papillary urothelial hyperplasia
MONDO:0024476	epithelial neoplasm of rectum
MONDO:0024475	squamous cell intraepithelial neoplasia
MONDO:0024478	mesenchymal hamartoma
MONDO:0024477	liver and intrahepatic bile duct neoplasm
MONDO:0024479	epithelial tumor of colon
MONDO:0024470	benign chondrogenic neoplasm
MONDO:0024472	boutonneuse fever
MONDO:0024471	non-inflammatory vasculopathy
MONDO:0024474	intraepithelial neoplasia
MONDO:0024473	Astrakhan spotted fever
MONDO:0012498	congenital stationary night blindness autosomal dominant 1
MONDO:0012499	Buruli ulcer, susceptibility to
MONDO:0012496	Koolen de Vries syndrome
MONDO:0012497	congenital stationary night blindness autosomal dominant 3
MONDO:0012490	cone-rod synaptic disorder, congenital nonprogressive
MONDO:0012491	macroglobulinemia, Waldenstrom, 2
MONDO:0036482	retinitis pigmentosa 81
MONDO:0012494	testicular microlithiasis
MONDO:0036483	short-rib thoracic dysplasia 18 with polydactyly
MONDO:0036484	Charcot-Marie-Tooth disease, dominant intermediate G
MONDO:0012495	spondyloepimetaphyseal dysplasia, Genevieve type
MONDO:0012492	restless legs syndrome, susceptibility to, 3
MONDO:0012493	restless legs syndrome, susceptibility to, 4
MONDO:0000498	arteritic anterior ischemic optic neuropathy
MONDO:0024465	surfactant metabolism dysfunction, pulmonary, 2
MONDO:0024464	pituitary hormone deficiency, combined, 1
MONDO:0000497	pyometritis
MONDO:0024467	apocrine sweat gland disease
MONDO:0000496	hemorrhagic cystitis
MONDO:0024466	facial paresis, hereditary congenital, 1
MONDO:0000495	oppositional defiant disorder
MONDO:0024469	chondrogenic neoplasm
MONDO:0024468	anterior pituitary gland disease
MONDO:0000499	non-arteritic anterior ischemic optic neuropathy
MONDO:0000490	glomerulosclerosis
MONDO:0024461	angiomatosis
MONDO:0000494	renal fibrosis
MONDO:0000493	Muckle-Wells syndrome
MONDO:0024460	Herpesviridae infections
MONDO:0024463	ovarian dysgenesis 1
MONDO:0000492	chronic venous insufficiency
MONDO:0024462	familial cutaneous melanoma
MONDO:0000491	limb ischemia
MONDO:0012487	alopecia-intellectual disability syndrome 2
MONDO:0012488	hepatitis B virus, susceptibility to
MONDO:0012485	autosomal recessive nonsyndromic deafness 68
MONDO:0012486	preauricular tag, isolated, autosomal dominant, 1
MONDO:0012489	cataract 23
MONDO:0036491	rare childhood malignant neoplasm
MONDO:0012480	diabetes mellitus, transient neonatal, 2
MONDO:0012483	cone-rod dystrophy 11
MONDO:0012484	prosopagnosia, hereditary
MONDO:0012481	mevalonic aciduria
MONDO:0012482	West Nile virus, susceptibility to
MONDO:0024454	sacral nerve plexus disease
MONDO:0024456	anterior segment dysgenesis 3
MONDO:0024455	autosomal dominant Robinow syndrome 1
MONDO:0024458	disease of visual system
MONDO:0024457	neurodegeneration with brain iron accumulation 2A
MONDO:0024459	Aeromonas hydrophila intestinal disease
MONDO:0012476	hereditary spastic paraplegia 30
MONDO:0012477	retinitis pigmentosa 33
MONDO:0012474	autosomal dominant nocturnal frontal lobe epilepsy 4
MONDO:0012475	cone dystrophy with supernormal rod response
MONDO:0012478	orofacial cleft 9
MONDO:0012479	congenital malabsorptive diarrhea 4
MONDO:0012472	Aicardi-Goutieres syndrome 4
MONDO:0012473	right pulmonary artery, anomalous origin of, familial
MONDO:0012470	prostate cancer, hereditary, 7
MONDO:0012471	Aicardi-Goutieres syndrome 3
MONDO:0024498	glioma susceptibility 1
MONDO:0024497	tumor grade 3 or 4, general grading system
MONDO:0024499	vascular bone neoplasm
MONDO:0024490	tumor grade X, general grading system
MONDO:0024492	tumor grade 2, general grading system
MONDO:0024491	tumor grade 1, general grading system
MONDO:0024494	tumor grade 4, general grading system
MONDO:0024493	tumor grade 3, general grading system
MONDO:0024496	tumor grade 2 or 3, general grading system
MONDO:0024495	tumor grade 1 or 2, general grading system
MONDO:0043494	arteritis
MONDO:0018480	carcinoma of esophagus, salivary gland type
MONDO:0018482	squamous cell carcinoma of stomach
MONDO:0018481	undifferentiated carcinoma of esophagus
MONDO:0006499	hamartoma
MONDO:0006497	cerebral palsy
MONDO:0006498	adenomatous colon polyp
MONDO:0006495	marginal zone B-cell lymphoma
MONDO:0006496	palsy
MONDO:0006493	Warthin tumor
MONDO:0006494	thyroid disease
MONDO:0006491	vulvar lichen sclerosus
MONDO:0006492	vulvar squamous cell carcinoma
MONDO:0006490	vaginal squamous cell carcinoma
MONDO:0018488	rare genetic odontal or periodontal disorder
MONDO:0018487	autosomal recessive severe congenital neutropenia due to CXCR2 deficiency
MONDO:0018489	autoimmune encephalopathy with parasomnia and obstructive sleep apnea
MONDO:0018484	semicircular canal dehiscence syndrome
MONDO:0018483	secondary pulmonary alveolar proteinosis
MONDO:0018486	visual snow syndrome
MONDO:0018485	glycogen storage disease due to acid maltase deficiency, late-onset
MONDO:0018471	generalized eruptive keratoacanthoma
MONDO:0018470	renal agenesis
MONDO:0043455	humoral hypercalcemia of malignancy
MONDO:0043452	chromosome 8, trisomy
MONDO:0018477	bilirubin encephalopathy
MONDO:0018476	dystonia-aphonia syndrome
MONDO:0018479	congenital adrenal hyperplasia
MONDO:0018478	primary hyperoxaluria
MONDO:0018473	hyperlipoproteinemia type 3
MONDO:0018472	familial isolated trichomegaly
MONDO:0018475	PRKAR1B-related neurodegenerative dementia with intermediate filaments
MONDO:0018474	13q12.3 microdeletion syndrome
MONDO:0018460	Eales disease
MONDO:0006479	undifferentiated pancreatic carcinoma with osteoclast-like giant cells
MONDO:0006477	undifferentiated ovarian carcinoma
MONDO:0006478	undifferentiated pancreatic carcinoma
MONDO:0043465	achlorhydria
MONDO:0043468	acne keloid
MONDO:0006475	unclassified renal cell carcinoma
MONDO:0006476	undifferentiated gallbladder carcinoma
MONDO:0006473	tracheal squamous cell carcinoma
MONDO:0006474	transitional cell carcinoma
MONDO:0006471	tracheal adenoid cystic carcinoma
MONDO:0006472	tracheal carcinoma
MONDO:0006470	tonsillar squamous cell carcinoma
MONDO:0031481	microcephaly, epilepsy, and diabetes syndrome 1
MONDO:0043459	radiation-induced disorder
MONDO:0043458	radiation injury
MONDO:0018469	pulmonary non-tuberculous mycobacterial infection
MONDO:0018466	hereditary late onset Parkinson disease
MONDO:0018465	insulin autoimmune syndrome
MONDO:0018468	proton-pump inhibitor-responsive esophageal eosinophilia
MONDO:0018467	nephropathic infantile cystinosis
MONDO:0018462	Angelman syndrome due to imprinting defect in 15q11-q13
MONDO:0018461	Angelman syndrome due to a point mutation
MONDO:0018464	severe phosphoribosylpyrophosphate synthetase superactivity
MONDO:0018463	mild phosphoribosylpyrophosphate synthetase superactivity
MONDO:0006488	vaginal carcinosarcoma
MONDO:0006489	vaginal melanoma
MONDO:0006486	uveal melanoma
MONDO:0043479	adenoviridae infectious disease
MONDO:0006487	vaginal adenoid cystic carcinoma
MONDO:0006484	usual ductal breast hyperplasia
MONDO:0043472	ectopic ACTH secretion syndrome
MONDO:0006485	uterine carcinosarcoma
MONDO:0043475	Adams-Stokes syndrome
MONDO:0006482	ureter small cell carcinoma
MONDO:0006483	urothelial dysplasia
MONDO:0006480	undifferentiated pleomorphic sarcoma, inflammatory variant
MONDO:0006481	ureter carcinoma
MONDO:0018459	isolated glycerol kinase deficiency
MONDO:0018458	familial hypocalciuric hypercalcemia
MONDO:0018455	dysostosis of genetic origin with limb anomaly as a major feature
MONDO:0018454	dysostosis of genetic origin
MONDO:0018457	rare genetic bone development disorder
MONDO:0018456	polyarticular juvenile idiopathic arthritis
MONDO:0018451	X-linked distal hereditary motor neuropathy
MONDO:0018450	spinal muscular atrophy with respiratory distress type 2
MONDO:0018453	familial atypical multiple mole melanoma syndrome
MONDO:0018452	deficiency of the interleukin-36 receptor antagonist
MONDO:0031421	Olmsted syndrome
MONDO:0031439	short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies
MONDO:0043424	digestive system infectious disease
MONDO:0018491	3-phosphoglycerate dehydrogenase deficiency
MONDO:0018490	cono-spondylar dysplasia
MONDO:0018493	malignant hyperthermia of anesthesia
MONDO:0018492	hereditary clear cell renal cell carcinoma
MONDO:0031446	hypercholanemia, familial 1
MONDO:0018499	double outlet right ventricle with atrioventricular septal defect, pulmonary stenosis, heterotaxy
MONDO:0018498	double outlet right ventricle with subaortic or doubly committed ventricular septal defect
MONDO:0018495	X-linked intellectual disability-limb spasticity-retinal dystrophy-diabetes insipidus syndrome
MONDO:0018494	microcephaly-short stature-intellectual disability-facial dysmorphism syndrome
MONDO:0018497	rare autonomic nervous system disorder
MONDO:0018496	ARX-related encephalopathy-brain malformation spectrum
MONDO:0006538	dermatitis herpetiformis
MONDO:0006539	diffuse lipomatosis
MONDO:0006536	congenital generalized lipodystrophy
MONDO:0006537	conjunctival pigmentation
MONDO:0006534	cholinergic urticaria
MONDO:0006535	cicatricial pemphigoid
MONDO:0006532	cholesteatoma of external ear
MONDO:0006533	cholesteatoma of middle ear
MONDO:0006530	cholesteatoma
MONDO:0006531	cholesteatoma of attic
MONDO:0018529	qualitative or quantitative defects of Torsin-1A-interacting protein 1
MONDO:0018528	congenital myopathy with myasthenic-like onset
MONDO:0018525	solid pseudopapillary carcinoma of pancreas
MONDO:0018524	intraductal papillary mucinous carcinoma of pancreas
MONDO:0018527	osteoclastic giant cell tumor of pancreas
MONDO:0018526	serous cystadenocarcinoma of pancreas
MONDO:0018521	squamous cell carcinoma of pancreas
MONDO:0018520	rare epithelial tumor of pancreas
MONDO:0018523	pancreatic mucinous cystadenoma
MONDO:0018522	acinar cell carcinoma of pancreas
MONDO:0006549	fibroepithelial polyp of the anus
MONDO:0006547	exanthem
MONDO:0006548	facial dermatosis
MONDO:0006545	erythema multiforme
MONDO:0006546	erythematosquamous dermatosis
MONDO:0006543	epidermolysis bullosa dystrophica
MONDO:0006544	erythema infectiosum
MONDO:0006541	epidermolysis bullosa
MONDO:0006542	epidermolysis bullosa acquisita
MONDO:0006540	dyshidrosis
MONDO:0018518	adenocarcinoma of the anal canal
MONDO:0018517	obsolete carcinoma of the anal canal
MONDO:0018519	squamous cell carcinoma of the anal canal
MONDO:0018514	rare epithelial tumor of rectum
MONDO:0018513	squamous cell carcinoma of colon
MONDO:0018516	epithelial tumor of anal canal
MONDO:0018515	squamous cell carcinoma of rectum
MONDO:0018510	small intestine neuroendocrine neoplasm
MONDO:0018512	rare epithelial tumor of colon
MONDO:0018511	epithelial tumor of the appendix
MONDO:0006518	sporadic Creutzfeld Jacob disease
MONDO:0006519	rectal cancer
MONDO:0006516	sarcopenia
MONDO:0006517	childhood malignant neoplasm
MONDO:0006514	recalcitrant atopic dermatitis
MONDO:0006515	acute pancreatitis
MONDO:0006512	estrogen-receptor positive breast cancer
MONDO:0006513	estrogen-receptor negative breast cancer
MONDO:0006510	renal tubular transport disease
MONDO:0006511	developmental dysplasia of the hip
MONDO:0018507	microcephaly-complex motor and sensory axonal neuropathy syndrome
MONDO:0018506	mesenchymal tumor of small intestine
MONDO:0018509	squamous cell carcinoma of the small intestine
MONDO:0018508	rare carcinoma of small intestine
MONDO:0018503	carcinoma of stomach, salivary gland type
MONDO:0018502	hereditary gastric cancer
MONDO:0018505	rare tumor of small intestine
MONDO:0018504	undifferentiated carcinoma of stomach
MONDO:0018501	rare carcinoma of stomach
MONDO:0018500	cutaneous larva migrans
MONDO:0006509	papillary carcinoma
MONDO:0006529	bullous skin disease
MONDO:0006527	anhidrosis
MONDO:0006528	bacterial exanthem
MONDO:0006525	allergic contact dermatitis
MONDO:0006526	allergic urticaria
MONDO:0006523	acrodermatitis
MONDO:0006524	acrodermatitis chronica atrophicans
MONDO:0006521	acneiform dermatitis
MONDO:0043510	brain injury
MONDO:0006522	acquired keratosis
MONDO:0043512	traumatic encephalopathy
MONDO:0006520	Achenbach syndrome
MONDO:0006578	mediastinal lipomatosis
MONDO:0006579	melanoacanthoma
MONDO:0006576	Ludwig's angina
MONDO:0006577	maxillary sinus cholesteatoma
MONDO:0006574	lipomatosis
MONDO:0006575	loiasis
MONDO:0006572	lichen planus
MONDO:0006573	lipodystrophy
MONDO:0006570	lichen disease
MONDO:0006571	lichen nitidus
MONDO:0018569	X-linked microcephaly-growth retardation-prognathism-cryptorchidism syndrome
MONDO:0018568	COG2-CDG
MONDO:0018565	congenital urachal anomaly
MONDO:0018564	3p25.3 microdeletion syndrome
MONDO:0018567	autosomal dominant Charcot-Marie-Tooth disease type 2 due to TFG mutation
MONDO:0018566	short stature-advanced bone age-early-onset osteoarthritis syndrome
MONDO:0018561	precocious puberty in female
MONDO:0018560	anterior urethral valve
MONDO:0018563	adactyly of foot
MONDO:0018562	genetic otorhinolaryngological malformation
MONDO:0006589	occupational dermatitis
MONDO:0006587	nodular nonsuppurative panniculitis
MONDO:0006588	nonepidermolytic palmoplantar keratoderma
MONDO:0006585	neurodermatitis
MONDO:0006586	neurotic excoriation
MONDO:0006583	necrobiosis lipoidica
MONDO:0006584	neonatal jaundice
MONDO:0006581	miliaria rubra
MONDO:0006582	mongolian spot
MONDO:0006580	miliaria
MONDO:0018558	syndrome with woolly hair
MONDO:0018557	rare genetic autonomic nervous system disorder
MONDO:0018559	fetal lower urinary tract obstruction
MONDO:0018554	pulmonary veno-occlusive disease and/or pulmonary capillary haemangiomatosis
MONDO:0018553	urachal diverticulum
MONDO:0018556	Lambert-Eaton myasthenic syndrome
MONDO:0018555	hypogonadotropic hypogonadism
MONDO:0018550	spastic paraplegia-optic atrophy-neuropathy and spastic paraplegia-optic atrophy-neuropathy-related disorder
MONDO:0018552	urachal sinus
MONDO:0018551	patent urachus
MONDO:0006558	pemphigoid gestationis
MONDO:0006559	hidradenitis suppurativa
MONDO:0006556	hand dermatosis
MONDO:0006557	hemangioma of subcutaneous tissue
MONDO:0006554	granuloma annulare
MONDO:0006555	granulomatous dermatitis
MONDO:0006552	folliculitis
MONDO:0006553	Fox-Fordyce disease
MONDO:0006550	fibroepithelial polyp of urethra
MONDO:0006551	alopecia mucinosa
MONDO:0018547	acute tricyclic antidepressant poisoning
MONDO:0018546	serotonin syndrome
MONDO:0018549	late-onset scapuloperoneal muscular dystrophy with hyaline bodies
MONDO:0018548	acute poisoning by drugs with membrane-stabilizing effect
MONDO:0018543	autosomal dominant hypocalcemia
MONDO:0018542	severe congenital neutropenia
MONDO:0018545	primary immunodeficiency with predisposition to severe viral infection
MONDO:0018544	adrenoleukodystrophy
MONDO:0018541	familial hypoaldosteronism
MONDO:0018540	PFAPA syndrome
MONDO:0006569	leg dermatosis
MONDO:0006567	kernicterus due to isoimmunization
MONDO:0006568	Kimura disease
MONDO:0006565	juvenile dermatitis herpetiformis
MONDO:0006566	keratosis
MONDO:0006563	inverted follicular keratosis
MONDO:0006564	irritant dermatitis
MONDO:0006561	eyelid hypopigmentation
MONDO:0006562	incontinentia pigmenti achromians
MONDO:0006560	hypohidrosis
MONDO:0018539	rare epithelial tumor of small intestine
MONDO:0018536	adenocarcinoma of gallbladder and extrahepatic biliary tract
MONDO:0018535	biliary cystadenocarcinoma
MONDO:0018538	inherited digestive cancer-predisposing syndrome
MONDO:0018537	squamous cell carcinoma of gallbladder and extrahepatic biliary tract
MONDO:0018532	adenocarcinoma of liver and intrahepatic biliary tract
MONDO:0018531	carcinoma of liver and intrahepatic biliary tract
MONDO:0018534	squamous cell carcinoma of liver and intrahepatic biliary tract
MONDO:0018533	undifferentiated carcinoma of liver and intrahepatic biliary tract
MONDO:0018530	rare epithelial tumor of liver and intrahepatic biliary tract
MONDO:0006507	hereditary hemochromatosis
MONDO:0006508	infantile epileptic encephalopathy
MONDO:0006505	basal ganglia cerebrovascular disease
MONDO:0006506	congenital nonspherocytic hemolytic anemia
MONDO:0006503	episodic ataxia
MONDO:0006504	acquired metabolic disease
MONDO:0006501	inflammatory skin disease
MONDO:0006502	acute respiratory distress syndrome
MONDO:0006500	hemangioma
MONDO:0043361	May-Thurner syndrome
MONDO:0043364	eosinophil peroxidase deficiency
MONDO:0031386	cardioacrofacial dysplasia
MONDO:0043370	secondary adrenal insufficiency
MONDO:0043377	juvenile spondyloarthropathy
MONDO:0043373	sudden sensorineural hearing loss
MONDO:0018361	neonatal scleroderma
MONDO:0018360	neonatal lupus erythematosus
MONDO:0006378	pleural epithelioid mesothelioma
MONDO:0006379	pleural mesothelioma
MONDO:0006376	plantar fibromatosis
MONDO:0006377	pleural biphasic mesothelioma
MONDO:0006374	placental choriocarcinoma
MONDO:0006375	placental hemangioma
MONDO:0006372	pituicytoma
MONDO:0043320	piriformis syndrome
MONDO:0006373	pituitary gland adenoma
MONDO:0006370	pineoblastoma
MONDO:0006371	pineocytoma
MONDO:0043317	amyopathic dermatomyositis
MONDO:0018367	clear cell adenocarcinoma of ovary
MONDO:0018366	mucinous adenocarcinoma of ovary
MONDO:0018369	immature ovarian teratoma
MONDO:0018368	primary peritoneal serous/papillary carcinoma
MONDO:0018363	focal facial dermal dysplasia
MONDO:0018362	persistent idiopathic facial pain
MONDO:0018365	malignant non-epithelial tumor of ovary
MONDO:0018364	malignant epithelial tumor of ovary
MONDO:0018350	malignant tumor of penis
MONDO:0006389	prostate rhabdomyosarcoma
MONDO:0006387	primary pulmonary diffuse large B-cell lymphoma
MONDO:0006388	prolactin-producing pituitary gland carcinoma
MONDO:0006385	primary intraosseous squamous cell carcinoma
MONDO:0043330	Mirizzi syndrome
MONDO:0006386	primary peritoneal serous adenocarcinoma
MONDO:0006383	primary cutaneous diffuse large B-cell lymphoma, Leg type
MONDO:0006384	primary effusion lymphoma
MONDO:0006381	plexiform ameloblastoma
MONDO:0006382	poorly differentiated thyroid gland carcinoma
MONDO:0006380	pleural sarcomatoid mesothelioma
MONDO:0043327	cerebrospinal fluid leak
MONDO:0018359	neonatal dermatomyositis
MONDO:0018356	secondary neonatal autoimmune disease
MONDO:0018355	Prader-Willi-like syndrome due to point mutation
MONDO:0018358	neonatal autoimmune hemolytic anemia
MONDO:0018357	neonatal antiphospholipid syndrome
MONDO:0018352	squamous cell carcinoma of penis
MONDO:0018351	adenocarcinoma of penis
MONDO:0018354	Prader-Willi-like syndrome
MONDO:0018353	refractory celiac disease
MONDO:0021994	Berk-Tabatznik syndrome
MONDO:0006358	parotid gland squamous cell carcinoma
MONDO:0006359	neoplasm with perivascular epithelioid cell differentiation
MONDO:0006356	parotid gland adenoid cystic carcinoma
MONDO:0006357	parotid gland carcinoma ex pleomorphic adenoma
MONDO:0006354	parathyroid hyperplasia
MONDO:0006355	parotid gland acinic cell carcinoma
MONDO:0043346	progressive transformation of germinal centers
MONDO:0006352	paranasal sinus adenoid cystic carcinoma
MONDO:0006353	paranasal sinus Schneiderian papilloma
MONDO:0043343	Chilaiditi syndrome
MONDO:0006350	papillary transitional cell carcinoma
MONDO:0006351	parachordoma
MONDO:0018349	MAN1B1-CDG
MONDO:0018348	polyglucosan body myopathy type 1
MONDO:0043339	lathyrism
MONDO:0018345	T+ B+ severe combined immunodeficiency
MONDO:0018344	periodic paralysis with transient compartment-like syndrome
MONDO:0018347	severe intellectual disability-progressive postnatal microcephaly- midline stereotypic hand movements syndrome
MONDO:0018346	ferro-cerebro-cutaneous syndrome
MONDO:0018341	3q27.3 microdeletion syndrome
MONDO:0018340	hereditary isolated aplastic anemia
MONDO:0018343	periodic paralysis with later-onset distal motor neuropathy
MONDO:0018342	Joubert syndrome with Jeune asphyxiating thoracic dystrophy
MONDO:0006369	pineal parenchymal tumor of intermediate differentiation
MONDO:0006367	pharyngeal adenoid cystic carcinoma
MONDO:0043355	collagenous gastritis
MONDO:0006368	phosphaturic mesenchymal tumor
MONDO:0043358	engraftment syndrome
MONDO:0006365	Peutz-Jeghers polyp
MONDO:0006366	Peutz-Jeghers polyp of the stomach
MONDO:0043352	fournier gangrene
MONDO:0006363	peritoneal multicystic mesothelioma
MONDO:0006364	peritoneal well differentiated papillary mesothelioma
MONDO:0006361	penile fibromatosis
MONDO:0006362	peritoneal mesothelioma
MONDO:0006360	penile carcinoma
MONDO:0018338	activated PI3K-delta syndrome
MONDO:0043349	intravascular papillary endothelial hyperplasia
MONDO:0018337	severe neonatal lactic acidosis due to NFS1-ISD11 complex deficiency
MONDO:0018339	PrP systemic amyloidosis
MONDO:0018334	chronic hiccup
MONDO:0018333	multiple acyl-CoA dehydrogenase deficiency, mild type
MONDO:0021977	basaloid follicular hamartoma
MONDO:0018336	Silver-Russell syndrome due to a point mutation
MONDO:0018335	deep dermatophytosis
MONDO:0021979	Basaran Yilmaz syndrome
MONDO:0018330	mucinous adenocarcinoma of the appendix
MONDO:0018332	multiple acyl-CoA dehydrogenase deficiency, severe neonatal type
MONDO:0018331	rare genetic dystonia
MONDO:0033954	monoclonal mast cell activation syndrome
MONDO:0018392	male infertility with spermatogenesis disorder due to single gene mutation
MONDO:0018391	male infertility with spermatogenesis disorder
MONDO:0018394	male infertility with teratozoospermia due to single gene mutation
MONDO:0018393	male infertility with azoospermia or oligozoospermia due to single gene mutation
MONDO:0033969	inflammatory bowel disease-recurrent sinopulmonary infections syndrome
MONDO:0033968	immune dysregulation-inflammatory bowel disease-arthritis-recurrent infections-lymphopenia syndrome
MONDO:0033967	immune dysregulation with inflammatory bowel disease
MONDO:0018390	male infertility due to sperm disorder
MONDO:0018399	rare disorder with female infertility due to a congenital hypogonadotropic hypogonadism
MONDO:0018396	rare male fertility disorder with obstructive azoospermia
MONDO:0018395	male infertility due to sperm motility disorder
MONDO:0018398	female infertility due to a congenital hypogonadotropic hypogonadism
MONDO:0018397	female infertility due to hypothalamic-pituitary-gonadal axis disorder
MONDO:0018381	osteochondrosis
MONDO:0018380	idiopathic avascular necrosis
MONDO:0018383	osteonecrosis of genetic origin
MONDO:0018382	epiphysiolysis of the hip
MONDO:0043300	actinic cheilitis
MONDO:0006398	retroperitoneal inflammatory myofibroblastic tumor
MONDO:0043303	hyperacusis
MONDO:0006399	rhabdoid tumor of the kidney
MONDO:0006396	rectal villous adenoma
MONDO:0006397	renal cell carcinoma associated with Xp11.2 translocations/TFE3 gene fusions
MONDO:0006394	rectal tubular adenoma
MONDO:0006395	rectal tubulovillous adenoma
MONDO:0006392	rectal hyperplastic polyp
MONDO:0006393	rectal traditional serrated adenoma
MONDO:0006390	prostate small cell carcinoma
MONDO:0006391	pyloric gland adenoma
MONDO:0018389	male infertility due to gonadal dysgenesis or sperm disorder
MONDO:0018388	rare male infertility due to testicular endocrine disorder
MONDO:0018385	osteochondrosis of genetic origin
MONDO:0033981	krt1-related diffuse nonepidermolytic keratoderma
MONDO:0018384	avascular necrosis of genetic origin
MONDO:0033980	RELA fusion-positive ependymoma
MONDO:0018387	rare male infertility due to adrenal disorder
MONDO:0018386	rare male infertility due to hypothalamic-pituitary-gonadal axis disorder
MONDO:0018370	KLHL9-related early-onset distal myopathy
MONDO:0018372	osteonecrosis
MONDO:0018371	nebulin-related early-onset distal myopathy
MONDO:0043314	aquarium granuloma
MONDO:0043310	amaurosis fugax
MONDO:0018378	osteonecrosis of the jaw
MONDO:0018377	rare hereditary disease with avascular necrosis
MONDO:0031332	Glanzmann thrombasthenia 1
MONDO:0018379	primary avascular necrosis
MONDO:0018374	secondary avascular necrosis
MONDO:0018373	avascular necrosis
MONDO:0018376	secondary non-traumatic avascular necrosis
MONDO:0018375	traumatic avascular necrosis
MONDO:0006419	small intestinal intraepithelial neoplasia
MONDO:0006417	small intestinal diffuse large B-cell lymphoma
MONDO:0006418	small intestinal enteropathy-associated T-cell lymphoma
MONDO:0006415	small intestinal adenocarcinoma
MONDO:0006416	small intestinal Burkitt lymphoma
MONDO:0006414	skin sarcoma
MONDO:0006411	sinonasal undifferentiated carcinoma
MONDO:0006412	sinus histiocytosis with massive lymphadenopathy
MONDO:0006410	simple endometrial hyperplasia
MONDO:0018408	cystic echinococcosis
MONDO:0018407	male infertility due to obstructive azoospermia of genetic origin
MONDO:0018409	rare genetic disorder with obstructive azoospermia
MONDO:0018404	rare genetic male infertility
MONDO:0018403	female infertility due to an implantation defect
MONDO:0018406	rare male infertility due to adrenal disorder of genetic origin
MONDO:0018405	rare male infertility due to hypothalamic-pituitary-gonadal axis disorder of genetic origin
MONDO:0018400	rare female infertility due to an adrenal disorder
MONDO:0018402	female infertility due to gonadal dysgenesis
MONDO:0018401	female infertility due to an anomaly of ovarian function
MONDO:0006428	splenic diffuse large B-cell lymphoma
MONDO:0006429	splenic hodgkin lymphoma
MONDO:0006426	spinal cord primitive neuroectodermal tumor
MONDO:0006427	spindle cell melanoma
MONDO:0006424	soft tissue neoplasm
MONDO:0006425	spinal chordoma
MONDO:0006422	small intestinal tubulovillous adenoma
MONDO:0006423	soft tissue chondroma
MONDO:0006420	small intestinal mucosa-associated lymphoid tissue lymphoma
MONDO:0006421	small intestinal tubular adenoma
MONDO:0006408	sex hormone-producing adrenal cortex adenoma
MONDO:0006409	signet ring cell gastric adenocarcinoma
MONDO:0006406	sarcomatoid carcinoma
MONDO:0006407	sarcomatoid mesothelioma
MONDO:0006404	salivary gland large cell carcinoma
MONDO:0006405	salivary gland small cell carcinoma
MONDO:0006402	salivary gland basal cell adenocarcinoma
MONDO:0006403	salivary gland carcinoma ex pleomorphic adenoma
MONDO:0006400	salivary gland acinic cell carcinoma
MONDO:0006401	salivary gland adenosquamous carcinoma
MONDO:0006459	thymoma type B1
MONDO:0006457	thymoma type AB
MONDO:0006458	thymoma type B3
MONDO:0006455	thymic undifferentiated carcinoma
MONDO:0006456	thymoma
MONDO:0006453	thymic small cell carcinoma
MONDO:0006454	thymic squamous cell carcinoma
MONDO:0006451	thymic carcinoma
MONDO:0006452	thymic sarcomatoid carcinoma
MONDO:0006450	therapy-related myeloid neoplasm
MONDO:0018448	clear cell papillary renal cell carcinoma
MONDO:0018447	chondromyxoid fibroma
MONDO:0018449	acquired cystic disease-associated renal cell carcinoma
MONDO:0018444	female infertility due to fertilization defect
MONDO:0018443	FBLN1-related developmental delay-central nervous system anomaly-syndactyly syndrome
MONDO:0018446	autosomal recessive cerebellar ataxia - epilepsy - intellectual disability syndrome
MONDO:0018445	global developmental delay - lung cysts - overgrowth - Wilms tumor syndrome
MONDO:0018440	autosomal recessive distal renal tubular acidosis
MONDO:0018442	acitretin/etretinate embryopathy
MONDO:0018441	hepatitis delta
MONDO:0006468	thyroid gland undifferentiated (anaplastic) carcinoma
MONDO:0006469	tibial adamantinoma
MONDO:0006466	thyroid gland spindle cell tumor with thymus-like differentiation
MONDO:0006467	thyroid gland squamous cell carcinoma
MONDO:0006464	thyroid gland mucosa-associated lymphoid tissue lymphoma
MONDO:0006465	thyroid gland oncocytic follicular carcinoma
MONDO:0006462	thyroid gland diffuse large B-cell lymphoma
MONDO:0006463	thyroid gland mucoepidermoid carcinoma
MONDO:0006460	thyroglossal duct cyst
MONDO:0006461	thyroid gland carcinoma
MONDO:0018437	acute myeloid leukemia with NPM1 somatic mutations
MONDO:0018436	megakaryoblastic acute myeloid leukemia with t(1;22)(p13;q13)
MONDO:0018439	eosinophilic colitis
MONDO:0018438	eosinophilic gastrointestinal disease
MONDO:0018433	acute myeloid leukemia with t(6;9)(p23;q34)
MONDO:0018432	lichen myxedematosus
MONDO:0018435	acute myeloid leukemia with inv3(p21;q26.2) or t(3;3)(p21;q26.2)
MONDO:0018434	acute myeloid leukemia with t(9;11)(p22;q23)
MONDO:0018431	cold-induced sweating syndrome - hyperthermia spectrum
MONDO:0018430	partial corpus callosum agenesis-cerebellar vermis hypoplasia with posterior fossa cysts syndrome
MONDO:0006439	syringocystadenoma papilliferum
MONDO:0006437	superficial fibromatosis
MONDO:0006438	synovial chondromatosis
MONDO:0006435	submandibular gland adenocarcinoma
MONDO:0006436	submandibular gland adenoid cystic carcinoma
MONDO:0006433	subcutaneous panniculitis-like T-cell lymphoma
MONDO:0006434	Subependymoma
MONDO:0006431	splenic marginal zone lymphoma
MONDO:0006432	stromal predominant kidney Wilms tumor
MONDO:0006430	splenic mantle cell lymphoma
MONDO:0018429	14q24.1q24.3 microdeletion syndrome
MONDO:0018426	AXIN2-related attenuated familial adenomatous polyposis
MONDO:0018425	Huntington disease-like syndrome due to C9ORF72 expansions
MONDO:0018428	9q31.1q31.3 microdeletion syndrome
MONDO:0018427	fibrolamellar carcinoma
MONDO:0018422	autosomal recessive spastic paraplegia type 70
MONDO:0018421	autosomal recessive spastic paraplegia type 69
MONDO:0018424	inherited lipoic acid biosynthesis defect
MONDO:0018423	autosomal recessive spastic paraplegia type 71
MONDO:0018420	autosomal recessive spastic paraplegia type 68
MONDO:0006448	testicular teratoma (disease)
MONDO:0006449	testicular yolk sac tumor
MONDO:0006446	testicular embryonal carcinoma
MONDO:0006447	testicular non-seminomatous germ cell tumor
MONDO:0006444	teratoma with malignant transformation
MONDO:0006445	testicular choriocarcinoma
MONDO:0006442	tendon sheath fibroma
MONDO:0006443	tenosynovial giant cell tumor
MONDO:0006440	systemic mastocytosis with associated clonal hematological non-mast-cell lineage disease
MONDO:0006441	T-cell prolymphocytic leukemia
MONDO:0018419	autosomal recessive spastic paraplegia type 67
MONDO:0018418	autosomal recessive spastic paraplegia type 66
MONDO:0018415	hymenolepiasis
MONDO:0018414	female infertility due to an implantation defect of genetic origin
MONDO:0018417	autosomal recessive spastic paraplegia type 60
MONDO:0018416	autosomal recessive spastic paraplegia type 59
MONDO:0018411	rare female infertility due to hypothalamic-pituitary-gonadal axis disorder of genetic origin
MONDO:0018410	rare genetic female infertility
MONDO:0018413	female infertility due to an anomaly of ovarian function of genetic origin
MONDO:0018412	rare female infertility due to adrenal disorder of genetic origin
MONDO:0043283	silicosiderosis
MONDO:0043280	Wallerian degeneration
MONDO:0043287	superior vena cava syndrome
MONDO:0043294	linear scleroderma
MONDO:0043291	Rokitansky-Aschoff sinuses of the gallbladder
MONDO:0043297	vibrio vulnificus infectious disease
MONDO:0018293	congenital disorder of glycosylation with skin involvement
MONDO:0018292	congenital disorder of glycosylation-related bone disorder
MONDO:0018295	congenital disorder of glycosylation with deafness as a major feature
MONDO:0018294	congenital disorder of glycosylation with nephropathy as a major feature
MONDO:0018291	congenital disorder of glycosylation with intestinal involvement
MONDO:0018290	congenital disorder of glycosylation with cardiac malformation as a major feature
MONDO:0018297	hypotonia-speech impairment-severe cognitive delay syndrome
MONDO:0018296	congenital disorder of glycosylation with developmental anomaly
MONDO:0018299	sphingolipidosis with epilepsy
MONDO:0018298	multicentric osteolysis-nodulosis-arthropathy spectrum
MONDO:0043240	hemophilic arthropathy
MONDO:0043247	Mallory-Weiss syndrome
MONDO:0043243	leukoplakia
MONDO:0043251	odontoma
MONDO:0043257	pemphigus and fogo selvagem
MONDO:0043254	papular urticaria
MONDO:0043267	rheumatoid vasculitis
MONDO:0043264	post-traumatic epilepsy
MONDO:0043275	TORCH syndrome
MONDO:0043277	mosaic trisomy 6
MONDO:0031219	mismatch repair cancer syndrome
MONDO:0018240	TRPV4-related bone disorder
MONDO:0021895	temporomandibular joint dysfunction syndrome
MONDO:0021896	anterior spinal artery stroke
MONDO:0006259	juvenile xanthogranuloma
MONDO:0006257	jejunal neuroendocrine tumor G1
MONDO:0006258	juvenile polyp
MONDO:0006255	intimal sarcoma
MONDO:0006256	invasive breast carcinoma
MONDO:0006253	infiltrating bladder urothelial carcinoma sarcomatoid variant
MONDO:0006254	intestinal type adenocarcinoma
MONDO:0006251	inclusion body fibromatosis
MONDO:0006252	infiltrating bladder lymphoepithelioma-like carcinoma
MONDO:0006250	ileal neuroendocrine tumor G1
MONDO:0018249	finger hyperphalangy - toe anomalies - severe pectus excavatum syndrome
MONDO:0018246	homozygous 2p21 microdeletion syndrome
MONDO:0018245	2p21 microdeletion syndrome without cystinuria
MONDO:0018248	intellectual disability-seizures-macrocephaly-obesity syndrome
MONDO:0033885	mitochondrial complex IV deficiency, nuclear-type
MONDO:0018247	CADDS
MONDO:0018242	autoimmune hypoparathyroidism
MONDO:0018241	primary short bowel syndrome
MONDO:0018244	obesity due to SIM1 deficiency
MONDO:0018243	intellectual disability-hyperkinetic movement-truncal ataxia syndrome
MONDO:0006268	liver diffuse large B-cell lymphoma
MONDO:0006269	liver inflammatory myofibroblastic tumor
MONDO:0006266	Leydig cell tumor
MONDO:0006267	liver cavernous hemangioma
MONDO:0006264	laryngeal adenoid cystic carcinoma
MONDO:0006265	laryngeal small cell carcinoma
MONDO:0006262	lacrimal gland adenoid cystic carcinoma
MONDO:0006263	Langerhans cell histiocytosis
MONDO:0006260	kidney medullary carcinoma
MONDO:0043209	albinism
MONDO:0043206	trichostasis spinulosa
MONDO:0018239	aggrecan-related bone disorder
MONDO:0018238	rare bone disease related to a common gene or pathway defect
MONDO:0043207	urethral obstruction sequence
MONDO:0018235	dysostosis with limb anomaly as a major feature
MONDO:0018234	dysostosis
MONDO:0018237	acrofacial dysostosis
MONDO:0021879	small cell variant anaplastic large cell lymphoma
MONDO:0018236	dysostosis with limb and face anomalies as a major feature
MONDO:0018231	primary bone dysplasia with progressive ossification of skin, skeletal muscle, fascia, tendons and ligaments
MONDO:0018230	primary bone dysplasia
MONDO:0018233	otopalatodigital syndrome spectrum disorder
MONDO:0018232	primary bone dysplasia with micromelia
MONDO:0031230	mitochondrial complex II deficiency, nuclear type
MONDO:0006239	head and neck paraganglioma
MONDO:0006237	granulocytic sarcoma
MONDO:0006238	growth hormone-producing pituitary gland adenoma
MONDO:0008899	camptodactyly syndrome, Guadalajara type 2
MONDO:0043224	multi-infarct dementia
MONDO:0006235	granular cell tumor
MONDO:0008898	camptodactyly syndrome, Guadalajara type 1
MONDO:0008897	tumoral calcinosis, hyperphosphatemic, familial, 1
MONDO:0006236	granular cell tumor of the neurohypophysis
MONDO:0008896	campomelia, Cumming type
MONDO:0043226	postpartum amenorrhea-galactorrhea syndrome
MONDO:0006233	gonadal teratoma
MONDO:0006234	grade III prostatic intraepithelial neoplasia
MONDO:0008895	hereditary arterial and articular multiple calcification syndrome
MONDO:0008894	cataract-hypertrichosis-intellectual disability syndrome
MONDO:0006231	gastrointestinal hamartoma
MONDO:0008893	C syndrome
MONDO:0006232	giant cell tumor of soft tissue
MONDO:0008892	progressive familial intrahepatic cholestasis type 1
MONDO:0006230	gastric squamous cell carcinoma
MONDO:0008891	riboflavin transporter deficiency
MONDO:0008890	progressive bulbar palsy
MONDO:0018228	bipartite talus
MONDO:0018227	hypocomplementemic urticarial vasculitis
MONDO:0043219	migraine with brainstem aura
MONDO:0018229	Stevens-Johnson syndrome
MONDO:0043218	neurovascular disease
MONDO:0018224	hydroa vacciniforme-like lymphoma
MONDO:0018223	systemic Epstein-Barr virus-positive T-cell lymphoproliferative disease of childhood
MONDO:0018226	infantile epileptic-dyskinetic encephalopathy
MONDO:0018225	ALK-positive large B-cell lymphoma
MONDO:0018222	X-linked intellectual disability due to GRIA3 anomalies
MONDO:0018221	immune hydrops fetalis
MONDO:0006248	hydatidiform mole
MONDO:0006249	hyperplastic polyp
MONDO:0006246	high grade surface osteosarcoma
MONDO:0006247	histiocytic and dendritic cell neoplasm
MONDO:0043237	glossodynia
MONDO:0006244	HER2 positive breast carcinoma
MONDO:0006245	hidradenocarcinoma
MONDO:0006242	hepatoblastoma
MONDO:0043230	ciguatera fish poisoning
MONDO:0006243	hepatoid adenocarcinoma
MONDO:0043233	exfoliative dermatitis
MONDO:0006240	hemangiopericytic neoplasm
MONDO:0006241	hepatic granuloma
MONDO:0018217	Koolen-de Vries syndrome due to a point mutation
MONDO:0018216	17q21.31 microdeletion syndrome
MONDO:0018218	autosomal recessive cerebral atrophy
MONDO:0018213	hereditary sensory and autonomic neuropathy type 1
MONDO:0018212	familial cervical artery dissection
MONDO:0018215	paraneoplastic neurologic syndrome
MONDO:0021856	Alsing syndrome
MONDO:0018214	generalized epilepsy with febrile seizures plus
MONDO:0018211	Balint syndrome
MONDO:0018210	Alexander disease type II
MONDO:0018282	qualitative or quantitative defects of alpha-dystroglycan
MONDO:0033839	osteoradionecrosis of the mandible
MONDO:0018281	congenital muscular dystrophy with hyperlaxity
MONDO:0018284	congenital disorder of glycosylation with neurological involvement
MONDO:0033838	radiation-induced plexopathy
MONDO:0018283	primary qualitative or quantitative defects of alpha-dystroglycan
MONDO:0018280	muscle-eye-brain disease with bilateral multicystic leucodystrophy
MONDO:0006299	mediastinal neuroblastoma
MONDO:0006297	maxillary sinus adenoid cystic carcinoma
MONDO:0006298	mediastinal malignant germ cell tumor
MONDO:0006295	malignant urinary system neoplasm
MONDO:0006296	mast cell sarcoma
MONDO:0006293	malignant mixed neoplasm
MONDO:0006294	pleural cancer
MONDO:0006291	malignant jugulotympanic paraganglioma
MONDO:0006292	malignant mesothelioma
MONDO:0006290	malignant germ cell tumor
MONDO:0018289	congenital disorder of glycosylation with dilated cardiomyopathy
MONDO:0018286	non-X-linked congenital disorder of glycosylation with intellectual disability as a major feature
MONDO:0018285	X-linked congenital disorder of glycosylation with intellectual disability as a major feature
MONDO:0018288	congenital disorder of glycosylation with hepatic involvement
MONDO:0018287	congenital disorder of glycosylation with epilepsy as a major feature
MONDO:0018271	peripheral primitive neuroectodermal tumor
MONDO:0018270	extraskeletal Ewing sarcoma
MONDO:0018273	XYLT1-CDG
MONDO:0018272	small cell carcinoma of the ovary
MONDO:0018279	congenital muscular dystrophy without intellectual disability
MONDO:0033853	congenital cataract-severe neonatal hepatopathy-global developmental delay syndrome
MONDO:0018278	congenital muscular dystrophy with intellectual disability
MONDO:0033850	autosomal recessive axonal charcot-marie-tooth disease due to copper metabolism defect
MONDO:0018275	salt and pepper syndrome
MONDO:0018274	GM3 synthase deficiency
MONDO:0018277	congenital muscular dystrophy with cerebellar involvement
MONDO:0018276	muscular dystrophy-dystroglycanopathy
MONDO:0018260	scalp syndrome
MONDO:0018262	fetal anticonvulsant syndrome
MONDO:0018261	Nevada syndrome
MONDO:0033856	LAMA5-related multisystemic syndrome
MONDO:0006279	lung sarcomatoid carcinoma
MONDO:0006277	lung lymphangioleiomyomatosis
MONDO:0006278	lung papilloma
MONDO:0006275	lung giant cell carcinoma
MONDO:0006276	lung inflammatory myofibroblastic tumor
MONDO:0006273	low grade fibromyxoid sarcoma with giant collagen rosettes
MONDO:0006274	low grade vulvar intraepithelial neoplasia
MONDO:0006271	low grade central osteosarcoma
MONDO:0006272	low grade fibromyxoid sarcoma
MONDO:0006270	lobular breast carcinoma in situ
MONDO:0018268	Medich giant platelet syndrome
MONDO:0033864	infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome
MONDO:0018267	combined cervical dystonia
MONDO:0033862	primary autoimmune enteropathy
MONDO:0018269	white platelet syndrome
MONDO:0018264	oculocutaneous albinism type 6
MONDO:0018263	fetal carbamazepine syndrome
MONDO:0018266	ataxia - telangiectasia variant
MONDO:0018265	rare disorder with dystonia and other neurologic or systemic manifestation
MONDO:0018251	glycogen storage disease due to phosphorylase kinase deficiency
MONDO:0018250	diffuse palmoplantar keratoderma with painful fissures
MONDO:0006288	malignant adrenal gland pheochromocytoma
MONDO:0006289	malignant epitheloid mesothelioma
MONDO:0006286	major salivary gland mucoepidermoid carcinoma
MONDO:0006287	malignancy in giant cell tumor of bone
MONDO:0006284	major salivary gland carcinoma
MONDO:0006285	major salivary gland carcinoma ex pleomorphic adenoma
MONDO:0006282	lymphangiosarcoma
MONDO:0006283	lymphoepithelioma-like lung carcinoma
MONDO:0006280	lung sclerosing hemangioma
MONDO:0006281	lung signet ring cell carcinoma
MONDO:0018257	familial syringomyelia
MONDO:0018256	acute myeloid leukemia with t(8;16)(p11;p13) translocation
MONDO:0018259	didymosis aplasticosebacea
MONDO:0018258	Angora hair nevus
MONDO:0018253	intellectual disability-facial dysmorphism-hand anomalies syndrome
MONDO:0018252	focal palmoplantar keratoderma with joint keratoses
MONDO:0018255	spondylometaphyseal dysplasia, Czarny-Ratajczak type
MONDO:0018254	spondyloepimetaphyseal dysplasia, Isidor type
MONDO:0008959	CHAND syndrome
MONDO:0008958	Klippel-Feil syndrome 2, autosomal recessive
MONDO:0008957	cervical vertebrae, agenesis of
MONDO:0008956	congenital neuronal ceroid lipofuscinosis
MONDO:0008955	cerebrooculofacioskeletal syndrome 1
MONDO:0008954	peroxisome biogenesis disorder 2A (Zellweger)
MONDO:0008953	peroxisome biogenesis disorder 1A (Zellweger)
MONDO:0008952	cerebrofaciothoracic dysplasia
MONDO:0008951	cerebrocortical degeneration of infancy
MONDO:0008950	cerebral sclerosis similar to Pelizaeus-Merzbacher disease
MONDO:0021929	traumatic myositis ossificans
MONDO:0021921	Arnold stickler bourne syndrome
MONDO:0021923	Arroyo Garcia Cimadevilla syndrome
MONDO:0021925	tracheobronchitis
MONDO:0021927	arthrogryposis epileptic seizures migrational brain disorder
MONDO:0006309	mucinous gastric adenocarcinoma
MONDO:0006307	mixed somatotroph-lactotroph pituitary gland adenoma
MONDO:0033926	prepubertal anorexia nervosa
MONDO:0008969	cholesterol pneumonia
MONDO:0033925	pediatric-onset Graves disease
MONDO:0008968	cholestasis with gallstone, ataxia, and visual disturbance
MONDO:0006305	mixed cell uveal melanoma
MONDO:0006306	mixed lobular and ductal breast carcinoma
MONDO:0008967	congenital bile acid synthesis defect 4
MONDO:0006303	middle ear squamous cell carcinoma
MONDO:0008966	Aagenaes syndrome
MONDO:0008965	CHARGE syndrome
MONDO:0006304	minor salivary gland adenocarcinoma
MONDO:0008964	congenital secretory chloride diarrhea 1
MONDO:0006301	metanephric adenoma
MONDO:0008963	Chediak-Higashi syndrome
MONDO:0006302	micropapillary serous carcinoma
MONDO:0008962	Griscelli syndrome type 1
MONDO:0008961	Charcot-Marie-Tooth disease type 4A
MONDO:0006300	medullomyoblastoma with myogenic differentiation
MONDO:0008960	Charcot-Marie-Tooth disease-deafness-intellectual disability syndrome
MONDO:0021918	arena syndrome
MONDO:0021910	aplasia cutis myopia
MONDO:0021913	aquagenic pruritus
MONDO:0021915	arakawa syndrome 2
MONDO:0008939	isolated cerebellar hypoplasia/agenesis
MONDO:0033939	hypohidrosis-electrolyte imbalance-lacrimal gland dysfunction-ichthyosis-xerostomia syndrome
MONDO:0008938	early-onset cerebellar ataxia with retained tendon reflexes
MONDO:0008937	cerebellar ataxia, benign, with thermoanalgesia
MONDO:0008936	cerebellar ataxia and neurosensory deafness
MONDO:0008935	cerebellar ataxia-hypogonadism syndrome
MONDO:0008934	cerebellar ataxia-ectodermal dysplasia syndrome
MONDO:0008933	cephalin lipidosis
MONDO:0008932	premature centromere division
MONDO:0008931	Cenani-Lenz syndactyly syndrome
MONDO:0008930	celiac disease, susceptibility to, 1
MONDO:0021907	aplasia cutis autosomal recessive
MONDO:0021908	aplasia cutis congenita dominant
MONDO:0021909	aplasia cutis congenita recessive
MONDO:0021902	aortopulmonary window
MONDO:0008929	cataract-intellectual disability-hypogonadism syndrome
MONDO:0021905	apert-like polydactyly syndrome
MONDO:0008949	cerebral malformation, seizures, hypertrichosis, and overlapping fingers
MONDO:0008948	cerebrotendinous xanthomatosis
MONDO:0033948	acquired angioedema with C1Inh deficiency
MONDO:0008947	bilateral striopallidodentate calcinosis
MONDO:0033947	hereditary angioedema with normal C1Inh
MONDO:0033946	hereditary angioedema with C1Inh deficiency
MONDO:0008946	cerebral angiopathy, dysphoric
MONDO:0008945	myoclonic cerebellar dyssynergia
MONDO:0008944	Joubert syndrome 1
MONDO:0008943	autosomal recessive spinocerebellar ataxia 2
MONDO:0008942	cerebelloparenchymal disorder II
MONDO:0008941	hepatic fibrosis-renal cysts-intellectual disability syndrome
MONDO:0008940	endosteal sclerosis-cerebellar hypoplasia syndrome
MONDO:0006338	ovarian germ cell tumor
MONDO:0021971	Baraitser Rodeck garner syndrome
MONDO:0006339	ovarian microcystic stromal tumor
MONDO:0008999	Cohen syndrome
MONDO:0006336	ovarian endometrioid adenocarcinoma with squamous differentiation
MONDO:0008998	Cockayne syndrome type 3
MONDO:0006337	ovarian endometriosis
MONDO:0008997	Cockayne syndrome A
MONDO:0006334	ovarian embryonal carcinoma
MONDO:0008996	COACH syndrome 1
MONDO:0006335	ovarian endometrioid adenocarcinoma
MONDO:0008995	Yunis-Varon syndrome
MONDO:0006332	ovarian choriocarcinoma
MONDO:0008994	cleidocranial dysplasia, recessive form
MONDO:0006333	ovarian dysgerminoma
MONDO:0008993	cleft palate-stapes fixation-oligodontia syndrome
MONDO:0006330	ossifying fibromyxoid tumor
MONDO:0008992	Juberg-Hayward syndrome
MONDO:0006331	ovarian carcinosarcoma
MONDO:0008991	Verloove Vanhorick-Brubakk syndrome
MONDO:0008990	cleft larynx, posterior
MONDO:0018327	glomus tumor
MONDO:0018326	transient neonatal myasthenia gravis
MONDO:0018329	persistent combined dystonia
MONDO:0018328	homozygous familial hypercholesterolemia
MONDO:0021964	bagatelle Cassidy syndrome
MONDO:0018323	HSD10 disease, neonatal type
MONDO:0018322	HSD10 disease, infantile type
MONDO:0018325	juvenile myasthenia gravis
MONDO:0021966	baker Vinters syndrome
MONDO:0018324	adult-onset myasthenia gravis
MONDO:0021969	Banti syndrome
MONDO:0018321	atypical juvenile parkinsonism
MONDO:0018320	primary microcephaly-mild intellectual disability-young-onset diabetes syndrome
MONDO:0021960	ureteritis
MONDO:0006349	papillary cystic neoplasm
MONDO:0006347	pancreatic large cell neuroendocrine carcinoma
MONDO:0021962	baetz-greenwalt syndrome
MONDO:0006348	pancreatic small cell neuroendocrine carcinoma
MONDO:0006345	palmar fibromatosis
MONDO:0006346	pancreatic acinar cell carcinoma
MONDO:0006343	ovarian transitional cell carcinoma
MONDO:0006344	ovarian yolk sac tumor
MONDO:0006341	ovarian small cell carcinoma
MONDO:0006342	ovarian squamous cell carcinoma
MONDO:0006340	ovarian serous adenofibroma
MONDO:0018319	familial episodic pain syndrome
MONDO:0018316	fatal post-viral neurodegenerative disorder
MONDO:0018315	X-linked osteoporosis with fractures
MONDO:0018318	disorder of asparagine metabolism
MONDO:0018317	growth retardation-mild developmental delay-chronic hepatitis syndrome
MONDO:0018312	histoplasmosis
MONDO:0021953	tuberculous fibrosis of lung
MONDO:0018311	acromelanosis
MONDO:0018314	infantile-onset mesial temporal lobe epilepsy with severe cognitive regression
MONDO:0018313	uveal melanoma
MONDO:0021957	autosomal recessive nonsyndromic congenital nuclear cataract
MONDO:0018310	Langerhans cell histiocytosis
MONDO:0006318	nevus of Ito
MONDO:0006319	nevus of Ota
MONDO:0006316	neuroblastic tumor
MONDO:0008979	chorea, benign familial
MONDO:0006317	neurothekeoma
MONDO:0008978	chordoma
MONDO:0021950	autoimmune oophoritis
MONDO:0006314	nasal cavity polyp
MONDO:0008977	chondrosarcoma
MONDO:0008976	chondroitin-6-sulfaturia, defective cellular immunity, nephrotic syndrome
MONDO:0021952	autoimmune progesterone dermatitis
MONDO:0006315	neoplastic medium-sized B-lymphocyte with basophilic cytoplasm
MONDO:0006312	myofibroma
MONDO:0008975	otospondylomegaepiphyseal dysplasia
MONDO:0006313	nabothian cyst
MONDO:0008974	Greenberg dysplasia
MONDO:0008973	chondrodysplasia punctata, Toriello type
MONDO:0006310	mucinuos carcinoma
MONDO:0006311	myelodysplastic/myeloproliferative Neoplasm
MONDO:0008972	rhizomelic chondrodysplasia punctata type 1
MONDO:0008971	chondrodysplasia calcificans Metaphysealis
MONDO:0008970	chondrodysplasia Blomstrand type
MONDO:0018309	Hirschsprung disease
MONDO:0018308	liver mesenchymal hamartoma
MONDO:0018305	chronic granulomatous disease
MONDO:0018304	Schnitzler syndrome
MONDO:0018307	neurodegeneration with brain iron accumulation
MONDO:0018306	Griscelli syndrome
MONDO:0018301	interstitial cystitis
MONDO:0021943	tuberculoma
MONDO:0018300	genetic hyperaldosteronism
MONDO:0021944	auditory neuropathy
MONDO:0018303	generalized isolated dystonia
MONDO:0018302	acquired kinky hair syndrome
MONDO:0021945	hearing disorder
MONDO:0021948	cutaneous tuberculosis
MONDO:0006329	olfactory neuroblastoma
MONDO:0006327	ocular sebaceous carcinoma
MONDO:0006328	odontogenic cyst
MONDO:0008989	citrulline transport defect
MONDO:0008988	citrullinemia type I
MONDO:0006325	ocular melanoma
MONDO:0021941	infection by Trypanosoma rhodesiense
MONDO:0006326	ocular melanoma with extraocular extension
MONDO:0008987	cirrhosis, familial
MONDO:0008986	circumvallate placenta syndrome
MONDO:0006323	non-seminomatous lesion
MONDO:0006324	normal breast-like subtype of breast carcinoma
MONDO:0008985	ciliary dyskinesia with transposition of ciliary microtubules
MONDO:0006321	non-functioning adrenal cortex adenoma
MONDO:0008984	ciliary discoordination due to random ciliary orientation
MONDO:0008983	chromosomal instability with tissue-specific radiosensitivity
MONDO:0006322	non-neoplastic bile duct disorder
MONDO:0008982	central areolar choroidal dystrophy
MONDO:0008981	infantile choroidocerebral calcification syndrome
MONDO:0006320	non-cutaneous melanoma
MONDO:0008980	ataxia-hypogonadism-choroidal dystrophy syndrome
MONDO:0021932	infection by Trypanosoma gambiense
MONDO:0021935	aspergillus niger infection
MONDO:0021937	Asrar Facharzt Haque syndrome
MONDO:0008917	heart defects-limb shortening syndrome
MONDO:0008916	cardiomyopathy associated with myopathy and sudden death
MONDO:0008915	dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome
MONDO:0008914	cardioauditory syndrome of Sanchez Cascos
MONDO:0008913	cardiac valvular defect, developmental
MONDO:0008912	cardiac septal defects with coarctation of the aorta
MONDO:0008911	cardiac lipidosis, familial
MONDO:0008910	carboxypeptidase N deficiency
MONDO:0008909	congenital disorder of glycosylation, type i/IIx
MONDO:0008908	MGAT2-CDG
MONDO:0008907	PMM2-CDG
MONDO:0008928	cataract-ataxia-deafness syndrome
MONDO:0008927	colobomatous optic disc-macular atrophy-chorioretinopathy syndrome
MONDO:0008926	COFS syndrome
MONDO:0008925	cataract 46 juvenile-onset
MONDO:0008924	congenital cataract-ichthyosis syndrome
MONDO:0008923	autosomal recessive palmoplantar keratoderma and congenital alopecia
MONDO:0008922	Sengers syndrome
MONDO:0008921	carnosinemia
MONDO:0008920	carnitine deficiency, myopathic
MONDO:0008919	systemic primary carnitine deficiency disease
MONDO:0008918	carnitine-acylcarnitine translocase deficiency
MONDO:0008906	carbimazole sensitivity
MONDO:0008905	predisposition to invasive fungal disease due to CARD9 deficiency
MONDO:0008904	camptomelic syndrome, long-limb type
MONDO:0008903	lung cancer
MONDO:0008902	camptodactyly-ichthyosis syndrome
MONDO:0008901	Tel Hashomer camptodactyly syndrome
MONDO:0008900	camptodactyly with fibrous tissue hyperplasia and skeletal dysplasia
MONDO:0043162	pagon stephan syndrome
MONDO:0043168	panostotic fibrous dysplasia
MONDO:0043164	palmer pagon syndrome
MONDO:0043166	pancreatic lipomatosis duodenal stenosis
MONDO:0043172	pfeiffer rockelein syndrome
MONDO:0018194	sex cord-stromal tumor of testis
MONDO:0018193	testicular teratoma
MONDO:0043174	Pfeiffer Tietze Welte syndrome
MONDO:0018196	germ cell tumor of testis
MONDO:0018195	non-seminomatous germ cell tumor of testis
MONDO:0018190	autosomal dominant childhood-onset proximal spinal muscular atrophy
MONDO:0043170	Pavone Fiumara Rizzo syndrome
MONDO:0018192	paratesticular adenocarcinoma
MONDO:0018191	tumor of testis and paratestis
MONDO:0043179	piepkorn karp hickok syndrome
MONDO:0043176	phosphoribosylpyrophosphate synthetase deficiency
MONDO:0018198	acute encephalopathy with biphasic seizures and late reduced diffusion
MONDO:0018197	mitochondrial DNA depletion syndrome, hepatocerebrorenal form
MONDO:0018199	new-onset refractory status epilepticus
MONDO:0018183	staphylococcal necrotizing pneumonia
MONDO:0043183	podder-tolmie syndrome
MONDO:0018182	bullous impetigo
MONDO:0043185	pointer syndrome
MONDO:0018185	congenital anomaly of the great veins
MONDO:0018184	gastric linitis plastica
MONDO:0018181	staphylococcal scalded skin syndrome
MONDO:0043181	Refsum disease with increased pipecolic acidemia
MONDO:0018180	staphylococcal scarlet fever
MONDO:0043187	pulmonary artery agenesis
MONDO:0006198	endometrial squamous cell carcinoma
MONDO:0006199	endometrial undifferentiated carcinoma
MONDO:0006196	endometrial serous adenocarcinoma
MONDO:0006197	endometrial small cell carcinoma
MONDO:0006194	endometrial mucinous adenocarcinoma
MONDO:0006195	endometrial polyp
MONDO:0006192	endometrial endometrioid adenocarcinoma
MONDO:0006193	endometrial hyperplasia without atypia
MONDO:0006190	endolymphatic sac tumor
MONDO:0006191	endometrial clear cell adenocarcinoma
MONDO:0018187	genetic syndromic Pierre Robin syndrome
MONDO:0018186	ring chromosome
MONDO:0018189	autosomal recessive cerebellar ataxia - pyramidal signs - nystagmus - oculomotor apraxia syndrome
MONDO:0018188	genetic intestinal polyposis
MONDO:0018172	malignant sex cord stromal tumor of ovary
MONDO:0018171	malignant germ cell tumor of ovary
MONDO:0043193	richieri-costa guion-almeida cohen syndrome
MONDO:0018174	hereditary glaucoma
MONDO:0043195	rubinstein taybi like syndrome
MONDO:0018173	acute opioid poisoning
MONDO:0018170	idiopathic nephrotic syndrome
MONDO:0043191	radial defect robin sequence
MONDO:0043197	ruvalcaba churesigaew myhre syndrome
MONDO:0043199	short limb dwarf lethal colavita kozlowski type
MONDO:0018179	bacterial toxic-shock syndrome
MONDO:0018176	polymicrogyria
MONDO:0018175	combined deficiency of factor V and factor VIII
MONDO:0018178	intestinal lymphangiectasia
MONDO:0018177	glioblastoma
MONDO:0043125	mcpherson robertson cammarano syndrome
MONDO:0043127	mehta lewis patton syndrome
MONDO:0043120	male pseudohermaphroditism due to defective lh molecule
MONDO:0043123	massa casaer ceulemans syndrome
MONDO:0043135	microcephaly microphthalmos blindness
MONDO:0043137	isolated microcephaly
MONDO:0043131	michels caskey syndrome
MONDO:0043133	microcephaly micropenis convulsions
MONDO:0043129	merlob grunebaum reisner syndrome
MONDO:0043141	microdontia hypodontia short stature
MONDO:0043143	microphthalmia microtia fetal akinesia
MONDO:0043139	microcephaly sparse hair intellectual disability seizures
MONDO:0031169	odontochondrodysplasia
MONDO:0043152	negative rheumatoid factor polyarthritis
MONDO:0043154	neonatal ovarian cyst
MONDO:0043156	nephrotic syndrome ocular anomalies
MONDO:0031178	monosomy 7 myelodysplasia and leukemia syndrome
MONDO:0006138	cervical large cell neuroendocrine carcinoma
MONDO:0006139	cervical metaplasia
MONDO:0008799	anophthalmia/microphthalmia-esophageal atresia syndrome
MONDO:0006136	cervical endometrioid adenocarcinoma
MONDO:0008798	nonsyndromic congenital nail disorder 4
MONDO:0006137	cervical intraepithelial neoplasia grade 2/3
MONDO:0006134	cervical adenosquamous carcinoma
MONDO:0008797	anodontia
MONDO:0008796	aniridia-renal agenesis-psychomotor retardation syndrome
MONDO:0006135	cervical clear cell adenocarcinoma
MONDO:0008795	aniridia-cerebellar ataxia-intellectual disability syndrome
MONDO:0006132	cervical adenoid basal carcinoma
MONDO:0008794	anhidrosis, familial generalized, with abnormal or absent sweat glands
MONDO:0006133	cervical adenoid cystic carcinoma
MONDO:0008793	angiomatosis, diffuse Corticomeningeal, of Divry and van Bogaert
MONDO:0006130	central nervous system neoplasm
MONDO:0006131	cerebellar liponeurocytoma
MONDO:0008792	familial angiolipomatosis
MONDO:0008791	isolated anencephaly/exencephaly
MONDO:0008790	anemia, nonspherocytic hemolytic, possibly due to defect in porphyrin metabolism
MONDO:0018129	autosomal recessive cerebellar ataxia with late-onset spasticity
MONDO:0018128	phalangeal microgeodic syndrome
MONDO:0018125	focal epilepsy-intellectual disability-cerebro-cerebellar malformation
MONDO:0018124	Oncogenic osteomalacia
MONDO:0018127	16q24.1 microdeletion syndrome
MONDO:0018126	progressive myoclonic epilepsy with dystonia
MONDO:0018121	mitochondrial DNA maintenance syndrome
MONDO:0018120	disorder of phospholipids, sphingolipids and fatty acids biosynthesis with skeletal muscle predominant involvement
MONDO:0018123	intellectual disability-obesity-brain malformations-facial dysmorphism syndrome
MONDO:0018122	digital anomalies-intellectual disability-short stature syndrome
MONDO:0021761	acral dysostosis dyserythropoiesis syndrome
MONDO:0021762	acrocoxomesomelic dysplasia
MONDO:0021764	acrofacial dysostosis preis type
MONDO:0006149	clear cell papillary cystadenoma
MONDO:0021765	radiculitis
MONDO:0006147	chronic eosinophilic leukemia, not otherwise specified
MONDO:0006148	chronic neutrophilic leukemia
MONDO:0006145	chondroid chordoma
MONDO:0006146	chondroid hamartoma
MONDO:0006143	cervical squamous cell carcinoma
MONDO:0006144	cervical Wilms tumor
MONDO:0006141	cervical villoglandular adenocarcinoma
MONDO:0006142	cervical small cell carcinoma
MONDO:0006140	cervical mucinous adenocarcinoma, minimal deviation variant
MONDO:0018118	disorder of phospholipids, sphingolipids and fatty acids biosynthesis with central nervous system predominant involvement
MONDO:0018117	disorder of phospholipids, sphingolipids and fatty acids biosynthesis
MONDO:0018119	disorder of phospholipids, sphingolipids and fatty acids biosynthesis with peripheral nerves predominant involvement
MONDO:0018114	isolated brachycephaly
MONDO:0018113	isolated plagiocephaly
MONDO:0018116	galactosemia
MONDO:0018115	epidermal nevus syndrome
MONDO:0021758	acquired agranulocytosis
MONDO:0018110	lethal idiopathic viral infection
MONDO:0021759	acquired fructose intolerance
MONDO:0018112	isolated scaphocephaly
MONDO:0018111	idiopathic severe pneumococcemia
MONDO:0021750	pyonephrosis
MONDO:0006118	breast fibrosis
MONDO:0006119	breast mucosa-associated lymphoid tissue lymphoma
MONDO:0021752	Achard-Thiers syndrome
MONDO:0008779	arthrogryposis
MONDO:0006116	breast carcinoma by gene expression profile
MONDO:0006117	breast diffuse large B-cell lymphoma
MONDO:0008778	amyloidosis, cutaneous bullous
MONDO:0008777	gelatinous drop-like corneal dystrophy
MONDO:0043103	hypothyroidism due to iodide transport defect
MONDO:0006114	bladder squamous cell carcinoma
MONDO:0008776	amyloidosis of gingiva and conjunctiva, with intellectual disability
MONDO:0006115	blast phase chronic myelogenous leukemia, BCR-ABL1 positive
MONDO:0006112	bladder inflammatory myofibroblastic tumor
MONDO:0008775	Amobarbital, deficient N-hydroxylation of
MONDO:0008774	2-aminoadipic 2-oxoadipic aciduria
MONDO:0006113	bladder small cell neuroendocrine carcinoma
MONDO:0006110	bladder adenocarcinoma
MONDO:0008773	amino aciduria with mental deficiency, dwarfism, muscular dystrophy, osteoporosis, and acidosis
MONDO:0008772	amelogenesis imperfecta type 2A1
MONDO:0006111	bladder flat intraepithelial lesion
MONDO:0008771	amelogenesis imperfecta type 1G
MONDO:0043101	hypothalamic dysfunction
MONDO:0008770	amelogenesis imperfecta type 1C
MONDO:0018107	idiopathic recurrent and disabling cutaneous herpes
MONDO:0018106	hereditary xanthinuria
MONDO:0018109	fulminant viral hepatitis
MONDO:0018108	idiopathic disseminated cytomegalovirus infection
MONDO:0018103	Quinquaud's folliculitis decalvans
MONDO:0018102	corneal dystrophy
MONDO:0021745	psychosocial short stature
MONDO:0018105	Wolfram syndrome
MONDO:0021746	pyelocystitis
MONDO:0018104	Torg-Winchester syndrome
MONDO:0021747	Acanthamoeba infectious disease
MONDO:0018101	familial primary hypomagnesemia with normocalciuria and normocalcemia
MONDO:0018100	familial primary hypomagnesemia
MONDO:0006129	central nervous system lymphoma
MONDO:0021742	puerperal infection
MONDO:0006127	cecum villous adenoma
MONDO:0008789	anemia, nonspherocytic hemolytic, associated with abnormality of red cell membrane
MONDO:0006128	central nervous system anaplastic large cell lymphoma
MONDO:0043114	Landy-Donnai syndrome
MONDO:0008788	IRIDA syndrome
MONDO:0006126	cecum neuroendocrine tumor G1
MONDO:0008787	microcytic anemia with liver iron overload
MONDO:0006123	cardiac rhabdomyoma
MONDO:0008786	pyridoxine-responsive sideroblastic anemia
MONDO:0043116	iida kannari syndrome
MONDO:0008785	sideroblastic anemia 2
MONDO:0006121	calcifying fibrous tumor
MONDO:0043110	jones hersh yusk syndrome
MONDO:0008784	autoimmune hemolytic anemia
MONDO:0008783	Tangier disease
MONDO:0006122	calcifying nested epithelial stromal tumor of the liver
MONDO:0008782	amyotrophic lateral sclerosis with polyglucosan bodies
MONDO:0043112	lachiewicz sibley syndrome
MONDO:0006120	C-cell hyperplasia
MONDO:0008781	juvenile amyotrophic lateral sclerosis with dementia
MONDO:0008780	amyotrophic lateral sclerosis type 2, juvenile
MONDO:0043106	ichthyosis linearis circumflexa
MONDO:0043108	infantile striato thalamic degeneration
MONDO:0021736	proctosigmoiditis
MONDO:0021739	prurigo
MONDO:0018161	non-hereditary retinoblastoma
MONDO:0018160	hereditary retinoblastoma
MONDO:0033717	congenital cerebellar ataxia due to RNU12 mutation
MONDO:0018163	autosomal recessive cutis laxa type 2A
MONDO:0018162	neurometabolic disorder due to serine deficiency
MONDO:0006178	dedifferentiated solitary fibrous tumor
MONDO:0006179	desmoplastic ameloblastoma
MONDO:0006176	cribriform carcinoma
MONDO:0006177	cutaneous undifferentiated pleomorphic sarcoma
MONDO:0006174	cortisol-producing adrenal cortex adenoma
MONDO:0006175	craniopharyngioma
MONDO:0006172	conjunctival nevus
MONDO:0006173	conjunctival squamous cell carcinoma
MONDO:0006170	conjunctival disorder
MONDO:0006171	conjunctival melanoma
MONDO:0018169	morning glory syndrome
MONDO:0018168	primary non-essential cutis verticis gyrata
MONDO:0018165	venous thoracic outlet syndrome
MONDO:0018164	arterial thoracic outlet syndrome
MONDO:0018167	primary essential cutis verticis gyrata
MONDO:0018166	oral submucous fibrosis
MONDO:0018150	Gaucher disease
MONDO:0018152	serpiginous choroiditis
MONDO:0018151	coenzyme Q10 deficiency
MONDO:0006189	eccrine porocarcinoma
MONDO:0006187	duodenal villous adenoma
MONDO:0006188	EBV-positive T-cell lymphoproliferative disorder of childhood
MONDO:0006185	ductal or ductular proliferation
MONDO:0006186	duodenal adenocarcinoma
MONDO:0006183	disseminated peritoneal leiomyomatosis
MONDO:0006184	ductal breast carcinoma in situ and lobular carcinoma in situ
MONDO:0006181	digestive system carcinoma
MONDO:0006182	digestive system mixed adenoneuroendocrine carcinoma
MONDO:0006180	digestive system adenoma
MONDO:0018158	mitochondrial DNA depletion syndrome
MONDO:0018157	mitochondrial disorder due to a defect in mitochondrial protein synthesis
MONDO:0018159	atypical hemolytic-uremic syndrome with DGKE deficiency
MONDO:0018154	Madelung deformity
MONDO:0018153	Erdheim-Chester disease
MONDO:0018156	3q26q27 microdeletion syndrome
MONDO:0018155	lateral sclerosis
MONDO:0018141	pyruvate carboxylase deficiency, infantile form
MONDO:0018140	burning mouth syndrome
MONDO:0006158	colorectal diffuse large B-cell lymphoma
MONDO:0006159	colorectal gastrointestinal stromal tumor
MONDO:0006156	colon sessile serrated adenoma/polyp
MONDO:0006157	colorectal adenosquamous carcinoma
MONDO:0006154	colon mucosa-associated lymphoid tissue lymphoma
MONDO:0006155	colon neuroendocrine tumor G1
MONDO:0006152	colon inflammatory polyp
MONDO:0006153	colon juvenile polyp
MONDO:0006150	colon Burkitt lymphoma
MONDO:0006151	colon dysplasia
MONDO:0018147	idiopathic macular telangiectasia type 3
MONDO:0018146	idiopathic macular telangiectasia type 1
MONDO:0018149	GM1 gangliosidosis
MONDO:0018148	vasoproliferative tumor of retina
MONDO:0018143	pyruvate carboxylase deficiency, benign type
MONDO:0018142	pyruvate carboxylase deficiency, severe neonatal type
MONDO:0018145	congenital retinal arteriovenous communication
MONDO:0018144	congenital myasthenic syndromes with glycosylation defect
MONDO:0018130	brain dopamine-serotonin vesicular transport disease
MONDO:0021783	streptococcal sore throat
MONDO:0006169	complex endometrial hyperplasia
MONDO:0006167	combined lung carcinoma
MONDO:0006168	common hematopoietic neoplasm
MONDO:0006165	colorectal squamous cell carcinoma
MONDO:0006166	columnar cell hyperplasia of the breast
MONDO:0006163	colorectal serrated adenocarcinoma
MONDO:0006164	colorectal sessile serrated adenoma/polyp
MONDO:0006161	colorectal juvenile polyp
MONDO:0006162	colorectal neuroendocrine tumor G1
MONDO:0006160	colorectal hamartoma
MONDO:0018139	scleredema
MONDO:0018136	minimal pigment oculocutaneous albinism type 1
MONDO:0021777	acute rheumatic heart disease
MONDO:0018135	oculocutaneous albinism type 1
MONDO:0018138	ocular albinism with congenital sensorineural deafness
MONDO:0018137	temperature-sensitive oculocutaneous albinism type 1
MONDO:0018132	congenital muscular alpha-dystroglycanopathy with brain and eye anomalies
MONDO:0018131	neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-hip dysplasia syndrome due to 9q21 microdeletion
MONDO:0018134	disorder of melanin metabolism
MONDO:0018133	attenuated Chédiak-Higashi syndrome
MONDO:0008839	ataxia-microcephaly-cataract syndrome
MONDO:0008838	ataxia - deafness - intellectual disability syndrome
MONDO:0008837	ataxia, deafness, and cardiomyopathy
MONDO:0008836	ataxia with myoclonic epilepsy and presenile dementia
MONDO:0008835	asthma, short stature, and elevated IgA
MONDO:0008834	asthma, nasal polyps, and aspirin intolerance
MONDO:0008833	renal-hepatic-pancreatic dysplasia 1
MONDO:0008832	right atrial isomerism
MONDO:0008831	asphyxiating thoracic dystrophy 1
MONDO:0008830	aspartylglucosaminuria
MONDO:0021808	acute cholinergic dysautonomia
MONDO:0021809	primary dysautonomia
MONDO:0021804	silicotuberculosis
MONDO:0021805	acromesomelic dysplasia, Campailla Martinelli type
MONDO:0008849	atrophoderma vermiculata
MONDO:0008848	atrioventricular dissociation
MONDO:0008847	atrichia with papular lesions
MONDO:0008846	atransferrinemia
MONDO:0008845	atonic-astatic syndrome of Foerster
MONDO:0008844	Athrombia, essential
MONDO:0008843	atherosclerosis-deafness-diabetes-epilepsy-nephropathy syndrome
MONDO:0008842	ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia
MONDO:0008841	ataxia-telangiectasia with generalized skin pigmentation and early death
MONDO:0008840	ataxia telangiectasia
MONDO:0033809	isolated blepharochalasis
MONDO:0033810	isolated iridoschisis
MONDO:0033818	Terrien marginal degeneration
MONDO:0008818	arterial tortuosity syndrome
MONDO:0008817	arterial calcification, generalized, of infancy, 1
MONDO:0008816	Chiari malformation type II
MONDO:0033816	thygeson superficial punctate keratopathy
MONDO:0008815	argininosuccinic aciduria
MONDO:0008814	hyperargininemia
MONDO:0008813	arachnoid cyst
MONDO:0008812	AREDYLD syndrome
MONDO:0008811	XK aprosencephaly
MONDO:0008810	familial apolipoprotein C-II deficiency
MONDO:0033821	fungal keratitis
MONDO:0008809	polyneuropathy-hand defect syndrome
MONDO:0008808	aplasia cutis congenita-intestinal lymphangiectasia syndrome
MONDO:0008829	chylous ascites
MONDO:0008828	camptodactyly-arthropathy-coxa vara-pericarditis syndrome
MONDO:0008827	progressive pseudorheumatoid arthropathy of childhood
MONDO:0008826	arthrogryposis-hyperkeratosis syndrome, lethal form
MONDO:0008825	arthrogryposis multiplex congenita-whistling face syndrome
MONDO:0008824	fetal akinesia deformation sequence
MONDO:0008823	arthrogryposis multiplex congenita 2, neurogenic type
MONDO:0008822	arthrogryposis, renal dysfunction, and cholestasis 1
MONDO:0008821	arthrogryposis, distal, with intellectual disability and characteristic facies
MONDO:0008820	arthrogryposis, distal, with hypopituitarism, intellectual disability, and facial anomalies
MONDO:0008819	arteriosclerosis, severe juvenile
MONDO:0006219	gallbladder small cell neuroendocrine carcinoma
MONDO:0006217	gallbladder adenosquamous carcinoma
MONDO:0008879	Bowen-Conradi syndrome
MONDO:0006218	gallbladder biliary intraepithelial neoplasia
MONDO:0021851	alopecia universalis onychodystrophy vitiligo
MONDO:0008878	bone dysplasia, lethal Holmgren type
MONDO:0006215	gallbladder adenocarcinoma
MONDO:0006216	gallbladder adenoma
MONDO:0008877	blue diaper syndrome
MONDO:0006213	floor of mouth mucoepidermoid carcinoma
MONDO:0008876	Bloom syndrome
MONDO:0008875	blepharophimosis-ptosis-esotropia-syndactyly-short stature syndrome
MONDO:0006214	follicular variant thyroid gland papillary carcinoma
MONDO:0008874	Bangstad syndrome
MONDO:0006211	fibrous hamartoma of infancy
MONDO:0008873	microcephalic osteodysplastic primordial dwarfism, type 3
MONDO:0006212	flat urothelial hyperplasia
MONDO:0008872	microcephalic osteodysplastic primordial dwarfism type II
MONDO:0006210	fibrolamellar hepatocellular carcinoma
MONDO:0008871	microcephalic osteodysplastic primordial dwarfism type I
MONDO:0008870	bird headed-dwarfism, Montreal type
MONDO:0018209	Alexander disease type I
MONDO:0018206	childhood-onset autosomal recessive myopathy with external ophthalmoplegia
MONDO:0018205	distal monosomy 1q
MONDO:0018208	neurofibromatosis type 1 due to NF1 mutation or intragenic deletion
MONDO:0018207	2p13.2 microdeletion syndrome
MONDO:0018202	gonadal germ cell tumor
MONDO:0018201	extragonadal germ cell tumor
MONDO:0021845	Aloi Tomasini Isaia syndrome
MONDO:0018204	20q11.2 microduplication syndrome
MONDO:0018203	LMNA-related cardiocutaneous progeria syndrome
MONDO:0021849	alopecia macular degeneration growth retardation syndrome
MONDO:0018200	acute encephalopathy with inflammation-mediated status epilepticus
MONDO:0006228	gastric papillary adenocarcinoma
MONDO:0006229	gastric small cell neuroendocrine carcinoma
MONDO:0006226	gastric mucosa-associated lymphoid tissue lymphoma
MONDO:0008889	thromboangiitis obliterans
MONDO:0008888	Williams-Campbell syndrome
MONDO:0006227	gastric neuroendocrine tumor G1
MONDO:0008887	bronchiectasis with or without elevated sweat chloride 1
MONDO:0006224	gastric hamartomatous polyp
MONDO:0006225	gastric mantle cell lymphoma
MONDO:0008886	Sabinas brittle hair syndrome
MONDO:0008885	Elsahy-Waters syndrome
MONDO:0006222	gastric choriocarcinoma
MONDO:0008884	oculoosteocutaneous syndrome
MONDO:0006223	gastric diffuse large B-cell lymphoma
MONDO:0006220	gallbladder squamous cell carcinoma
MONDO:0008883	brachydactyly, type A2, with microcephaly
MONDO:0006221	gastric adenoma
MONDO:0008882	congenital bowing of long bones
MONDO:0008881	kyphomelic dysplasia
MONDO:0008880	Bowen syndrome of multiple malformations
MONDO:0021834	Akaba Hayasaka syndrome
MONDO:0021836	Aksu von Stockhausen syndrome
MONDO:0021838	Al Gazali Khidr Prem Chandran syndrome
MONDO:0021839	spirochaetales infections
MONDO:0008859	berry aneurysm, cirrhosis, pulmonary emphysema, and cerebral calcification
MONDO:0008858	Behr syndrome
MONDO:0008857	Beemer-Ertbruggen syndrome
MONDO:0008856	immunodeficiency 27A
MONDO:0008855	MHC class II deficiency
MONDO:0008854	Bardet-Biedl syndrome 1
MONDO:0008853	Barber-Say syndrome
MONDO:0008852	congenital central hypoventilation syndrome
MONDO:0008851	autism
MONDO:0008850	Cooper-Jabs syndrome
MONDO:0021829	agnathia-microstomia-synotia
MONDO:0021824	adult progressive spinal muscular atrophy, Aran Duchenne type
MONDO:0021826	aerobic Actinomyces infection
MONDO:0006208	fallopian tube serous adenocarcinoma
MONDO:0006209	fibroblastic neoplasm
MONDO:0008869	Seckel syndrome 1
MONDO:0006206	fallopian tube carcinoma
MONDO:0006207	fallopian tube carcinosarcoma
MONDO:0008868	biliary malformation with renal tubular insufficiency
MONDO:0008867	biliary atresia
MONDO:0006204	extramammary Paget disease
MONDO:0008866	bifid nose, autosomal recessive
MONDO:0006205	extraskeletal Ewing sarcoma/peripheral primitive neuroectodermal tumor
MONDO:0006202	extrahepatic bile duct adenosquamous carcinoma
MONDO:0008865	Bietti crystalline corneoretinal dystrophy
MONDO:0008864	Biemond syndrome type 2
MONDO:0006203	extrahepatic bile duct squamous cell carcinoma
MONDO:0006200	epithelioid cell uveal melanoma
MONDO:0008863	sitosterolemia
MONDO:0006201	ethmoid sinus adenoid cystic carcinoma
MONDO:0008862	3-methylcrotonyl-CoA carboxylase 2 deficiency
MONDO:0008861	3-methylcrotonyl-CoA carboxylase 1 deficiency
MONDO:0008860	beta-aminoisobutyric acid, urinary excretion of
MONDO:0021811	acute mountain sickness
MONDO:0021812	adnexal spiradenoma/cylindroma of a sweat gland
MONDO:0008807	apnea, central sleep
MONDO:0008806	Aphalangy-hemivertebrae-urogenital-intestinal dysgenesis syndrome
MONDO:0008805	Takayasu's arteritis
MONDO:0008804	anus, imperforate
MONDO:0008803	Antley-Bixler syndrome
MONDO:0008802	antithrombin, familial hemorrhagic diathesis due to
MONDO:0008801	anosmia for isobutyric acid
MONDO:0008800	microphthalmia with limb anomalies
MONDO:0018084	Uhl anomaly
MONDO:0018083	transient tyrosinemia of the newborn
MONDO:0018086	ulerythema ophryogenesis
MONDO:0018085	umbilical cord ulceration-intestinal atresia syndrome
MONDO:0018080	rare germ cell tumor
MONDO:0018082	aorto-ventricular tunnel
MONDO:0018081	hemorrhagic fever-renal syndrome
MONDO:0006099	B-cell prolymphocytic leukemia
MONDO:0006097	atypical lipomatous tumor
MONDO:0006098	atypical lobular breast hyperplasia
MONDO:0006095	atypical carcinoid tumor
MONDO:0006096	atypical endometrial hyperplasia
MONDO:0006093	ascending colon neuroendocrine tumor G1
MONDO:0006094	Askin tumor
MONDO:0006091	appendix neuroendocrine tumor G1
MONDO:0006092	appendix villous adenoma
MONDO:0006090	appendix hyperplastic polyp
MONDO:0018088	familial Mediterranean fever
MONDO:0018087	viral hemorrhagic fever
MONDO:0018089	double outlet right ventricle
MONDO:0018072	persistent truncus arteriosus
MONDO:0018075	neural tube defect
MONDO:0018074	American trypanosomiasis
MONDO:0018071	trisomy 18
MONDO:0018070	familial multiple fibrofolliculoma
MONDO:0018077	tularemia
MONDO:0018076	tuberculosis
MONDO:0018079	thymic epithelial neoplasm
MONDO:0018078	soft tissue sarcoma
MONDO:0018062	autosomal dominant trichoodontoonychodysplasia-syndactyly
MONDO:0018061	trichodermodysplasia-dental alterations syndrome
MONDO:0018064	trigonocephaly-broad thumbs syndrome
MONDO:0018063	nodular non-suppurative panniculitis
MONDO:0018060	congenital fibrinogen deficiency
MONDO:0043069	Zerres Rietschel Majewski syndrome
MONDO:0006079	ameloblastic carcinoma
MONDO:0006077	adrenal medullary hyperplasia
MONDO:0006078	AIDS-related primary central nervous system lymphoma
MONDO:0006075	adrenal gland myelolipoma
MONDO:0006076	adrenal gland neuroblastoma
MONDO:0006073	adenomatoid odontogenic tumor
MONDO:0006074	adenosquamous carcinoma
MONDO:0006071	adenofibroma
MONDO:0006072	adenoid cystic breast carcinoma
MONDO:0006070	acute leukemia
MONDO:0018069	distal trisomy 17q
MONDO:0018066	trisomy X
MONDO:0018065	isolated trigonocephaly
MONDO:0018068	trisomy 13
MONDO:0018067	triploidy
MONDO:0018051	Jessner lymphocytic infiltration of the skin
MONDO:0043073	Zadik-Barak-Levin syndrome
MONDO:0018050	tibial aplasia-ectrodactyly syndrome
MONDO:0018053	trichothiodystrophy
MONDO:0043075	neuroaxonal dystrophy renal tubular acidosis
MONDO:0018052	hypoplastic tibiae-postaxial polydactyly syndrome
MONDO:0043071	Zazam Sheriff Phillips syndrome
MONDO:0006088	appendix adenoma
MONDO:0043077	weinstein kliman scully syndrome
MONDO:0006089	appendix goblet cell carcinoid
MONDO:0006086	angiomyxoma
MONDO:0043079	acute articular rheumatism
MONDO:0006087	appendix adenocarcinoma
MONDO:0006084	angioleiomyoma
MONDO:0006085	angiolipoma
MONDO:0006082	anal squamous cell carcinoma
MONDO:0006083	anaplastic large cell lymphoma, ALK-negative
MONDO:0006080	ampulla of vater carcinoma
MONDO:0006081	anal melanoma
MONDO:0018059	meningococcal meningitis
MONDO:0018058	tracheal agenesis
MONDO:0018055	pediatric hepatocellular carcinoma
MONDO:0018054	familial atrial fibrillation
MONDO:0018057	toxocariasis
MONDO:0018056	bullous lichen planus
MONDO:0043004	Weil's disease
MONDO:0043003	familial acanthosis nigricans
MONDO:0043005	genetic multiple congenital anomalies/dysmorphic syndrome
MONDO:0033683	congenital progressive bone marrow failure-B-cell immunodeficiency-skeletal dysplasia syndrome
MONDO:0033682	skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome
MONDO:0043008	genetic multiple congenital anomalies/dysmorphic syndrome without intellectual disability
MONDO:0043007	genetic multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome
MONDO:0043009	genetic lethal multiple congenital anomalies/dysmorphic syndrome
MONDO:0031037	famililal cerebral cavernous malformations
MONDO:0018095	Weaver-Williams syndrome
MONDO:0018094	Waardenburg syndrome
MONDO:0018097	West syndrome
MONDO:0018096	Weill-Marchesani syndrome
MONDO:0018091	microcephaly-brachydactyly-kyphoscoliosis syndrome
MONDO:0018090	double outlet left ventricle
MONDO:0018093	arbovirus fever
MONDO:0018092	Vogt-Koyanagi-Harada disease
MONDO:0018099	Whipple disease
MONDO:0018098	autosomal dominant limb-girdle muscular dystrophy type 1E (DES)
MONDO:0021650	uterine corpus neuroendocrine neoplasm
MONDO:0021651	synpolydactyly
MONDO:0033639	mitochondrial complex 4 deficiency, nuclear type 10
MONDO:0021652	diffuse type adenocarcinoma
MONDO:0006019	yaws
MONDO:0033638	mitochondrial complex 4 deficiency, nuclear type 8
MONDO:0033637	mitochondrial complex 4 deficiency, nuclear type 7
MONDO:0021653	cutaneous focal mucinosis
MONDO:0033636	mitochondrial complex 4 deficiency, nuclear type 4
MONDO:0021654	diffuse cutaneous mucinosis
MONDO:0006017	western equine encephalitis
MONDO:0033635	mitochondrial complex 4 deficiency, nuclear type 3
MONDO:0021655	secondary catabolic mucinosis of skin
MONDO:0008679	Wilms tumor 1
MONDO:0006018	Wissler syndrome
MONDO:0006015	Waterhouse-Friderichsen syndrome
MONDO:0008678	Williams syndrome
MONDO:0008677	widow's peak
MONDO:0006016	West Nile encephalitis
MONDO:0008676	white sponge nevus 1
MONDO:0006013	visna disease
MONDO:0006014	vulvovaginal candidiasis
MONDO:0008675	freeman-Sheldon syndrome
MONDO:0008674	WHIM syndrome
MONDO:0006011	viral hepatitis
MONDO:0006012	viral pneumonia
MONDO:0008673	acrofacial dysostosis, Weyers type
MONDO:0008672	Watson syndrome
MONDO:0008671	Waardenburg syndrome type 2A
MONDO:0006010	salmonid viral hemorrhagic septicemia
MONDO:0008670	Waardenburg syndrome type 1
MONDO:0018008	idiopathic giant cell myocarditis
MONDO:0018007	mosaic genome-wide paternal uniparental disomy
MONDO:0018009	non-hypoproteinemic hypertrophic gastropathy
MONDO:0018004	acute megakaryoblastic leukemia without down syndrome
MONDO:0033645	mitochondrial complex 4 deficiency, nuclear type 11
MONDO:0021645	esophageal varices with bleeding
MONDO:0018003	limbic encephalitis with DPP6 antibodies
MONDO:0033644	microcornea, rod-cone dystrophy, cataract, and posterior staphyloma 1
MONDO:0018006	adult-onset distal myopathy due to VCP mutation
MONDO:0033643	inflammatory bowel disease 30
MONDO:0033642	neurodevelopmental disorder with alopecia and brain abnormalities
MONDO:0018005	spastic paraplegia-Paget disease of bone syndrome
MONDO:0018000	hereditary thrombocytosis with transverse limb defect
MONDO:0033641	cleft palate, proliferative retinopathy, and developmental delay
MONDO:0033640	vitamin D-dependent rickets, type 3
MONDO:0018002	adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy
MONDO:0018001	inverse Klippel-Trenaunay syndrome
MONDO:0021640	grade III glioma
MONDO:0021641	Bunyaviridae infectious disease
MONDO:0033649	mitochondrial complex 4 deficiency, nuclear type 14
MONDO:0021642	vulval varices
MONDO:0006028	cecum adenocarcinoma
MONDO:0021643	mesenteric varices
MONDO:0006029	cecum carcinoma
MONDO:0033646	mitochondrial complex 4 deficiency, nuclear type 12
MONDO:0021644	esophageal varices without bleeding
MONDO:0006026	urinary bladder disease
MONDO:0008689	dehydrated hereditary stomatocytosis with or without pseudohyperkalemia and/or perinatal edema
MONDO:0008688	WT limb-blood syndrome
MONDO:0006027	breast synovial sarcoma
MONDO:0008687	Woronets trait
MONDO:0008686	isolated familial woolly hair disorder
MONDO:0006025	autosomal recessive disease
MONDO:0006022	acidosis disorder
MONDO:0008685	Wolff-Parkinson-white syndrome
MONDO:0008684	Wolf-Hirschhorn syndrome
MONDO:0008683	Wilms tumor 3
MONDO:0006020	Zollinger-Ellison syndrome
MONDO:0006021	Prinzmetal angina
MONDO:0008682	Denys-Drash syndrome
MONDO:0008681	WAGR syndrome
MONDO:0008680	Wilms tumor 2
MONDO:0021634	epithelial skin neoplasm
MONDO:0033656	mitochondrial complex 4 deficiency, nuclear type 21
MONDO:0033655	mitochondrial complex 4 deficiency, nuclear type 20
MONDO:0021635	neurocristopathy
MONDO:0033654	mitochondrial complex 4 deficiency, nuclear type 19
MONDO:0021636	astrocytic tumor
MONDO:0021637	low grade glioma
MONDO:0033653	mitochondrial complex 4 deficiency, nuclear type 18
MONDO:0021638	low grade astrocytic tumor
MONDO:0033652	mitochondrial complex 4 deficiency, nuclear type 17
MONDO:0033651	mitochondrial complex 4 deficiency, nuclear type 16
MONDO:0021639	grade II glioma
MONDO:0033650	mitochondrial complex 4 deficiency, nuclear type 15
MONDO:0021630	lipoma of face
MONDO:0008659	transcobalamin I deficiency
MONDO:0021631	brain astrocytoma
MONDO:0021632	primary brain neoplasm
MONDO:0033658	neurodevelopmental disorder with seizures and brain atrophy
MONDO:0008658	virus Rd114 RNA Complementarity
MONDO:0008657	vibratory angioedema
MONDO:0021633	cerebral astrocytoma
MONDO:0033657	leukodystrophy, hypomyelinating, 20
MONDO:0008656	benign paroxysmal positional nystagmus
MONDO:0008655	vestibulocochlear dysfunction, progressive
MONDO:0008654	nystagmus 4, congenital, autosomal dominant
MONDO:0008653	vesicoureteral reflux 1
MONDO:0008652	congenital vertical talus
MONDO:0008651	vertebral hypoplasia with lumbar kyphosis
MONDO:0008650	posterior fusion of lumbosacral vertebrae-blepharoptosis syndrome
MONDO:0033667	Delpire-McNeill syndrome
MONDO:0033665	deafness, autosomal dominant 78
MONDO:0031002	Baralle-Macken syndrome
MONDO:0033664	Kilquist syndrome
MONDO:0031003	hypercholanemia, familial, 2
MONDO:0021627	eyelid capillary hemangioma
MONDO:0031001	vitreoretinopathy with phalangeal epiphyseal dysplasia
MONDO:0021628	lacrimal system disease
MONDO:0033662	neurodevelopmental disorder with microcephaly, seizures, and brain atrophy
MONDO:0021629	uterine ligament neoplasm
MONDO:0031008	nephrotic syndrome, type 24
MONDO:0006008	vestibular neuronitis
MONDO:0006009	viral encephalitis
MONDO:0031009	Glanzmann thrombasthenia 2
MONDO:0006006	verrucous carcinoma
MONDO:0008669	vulvovaginitis, allergic seminal
MONDO:0031006	neurodegeneration with ataxia and late-onset optic atrophy
MONDO:0033669	Noonan syndrome 13
MONDO:0008668	von Willebrand disease 1
MONDO:0006007	vesicoureteral reflux
MONDO:0031007	spondyloepiphyseal dysplasia, sensorineural hearing loss, impaired intellectual development, and leber congenital amaurosis
MONDO:0033668	deafness, autosomal dominant 79
MONDO:0006004	vasomotor rhinitis
MONDO:0008667	von Hippel-Lindau disease
MONDO:0006005	Venezuelan equine encephalitis
MONDO:0008666	volvulus of midgut
MONDO:0008665	ptosis-vocal cord paralysis syndrome
MONDO:0006002	urogenital tuberculosis
MONDO:0006003	uterine corpus cancer
MONDO:0008664	autosomal dominant neovascular inflammatory vitreoretinopathy
MONDO:0006000	tuberculous peritonitis
MONDO:0008663	snowflake vitreoretinal degeneration
MONDO:0008662	autosomal dominant vitreoretinochoroidopathy
MONDO:0006001	urinary schistosomiasis
MONDO:0008661	vitiligo
MONDO:0008660	autosomal dominant hypophosphatemic rickets
MONDO:0033670	deafness, autosomal recessive 116
MONDO:0031013	autoimmune optic neuritis
MONDO:0031014	autoimmune gastritis
MONDO:0031011	neurodevelopmental disorder with dysmorphic facies and variable seizures
MONDO:0031012	autoimmune uveitis
MONDO:0033673	spermatogenic failure 46
MONDO:0033672	Duane anomaly-myopathy-scoliosis syndrome
MONDO:0033671	spermatogenic failure 45
MONDO:0031010	odontochondrodysplasia 2 with hearing loss and diabetes
MONDO:0018040	immunodeficiency with severe reduction in serum IgG and IgA with normal/elevated IgM and normal number of B-cells
MONDO:0018042	immunodeficiency syndrome with abnormal pigmentation
MONDO:0018041	other immunodeficiency syndrome with predominantly antibody defects
MONDO:0021697	chlamydia infectious disease
MONDO:0021698	alcohol-related disorders
MONDO:0021699	alcohol-induced disorders
MONDO:0006059	nasal cavity squamous cell carcinoma
MONDO:0006057	thymic lymphoma
MONDO:0006058	Wilms tumor
MONDO:0006055	sex cord-stromal tumor
MONDO:0006056	squamous cell breast carcinoma
MONDO:0006053	renal leiomyoma
MONDO:0006054	reproductive system neoplasm
MONDO:0006051	postweaning multisystemic wasting syndrome
MONDO:0006052	pulmonary tuberculosis
MONDO:0006050	pleomorphic breast carcinoma
MONDO:0018048	heparin-induced thrombocytopenia
MONDO:0018047	familial thrombomodulin anomalies
MONDO:0018049	Kaposi sarcoma
MONDO:0018044	idiopathic hypersomnia
MONDO:0018043	Thomas syndrome
MONDO:0018046	thrombocytopenia-robin sequence syndrome
MONDO:0018045	Hoyeraal-Hreidarsson syndrome
MONDO:0021681	sexually transmitted disease
MONDO:0021682	viral sexually transmitted disease
MONDO:0018031	granulomatous slack skin disease
MONDO:0021683	transmissible disease
MONDO:0018030	tetrasomy 9p
MONDO:0021684	infectious disease of central nervous system
MONDO:0006068	ACTH-producing pituitary gland adenoma
MONDO:0006069	ACTH-producing pituitary gland carcinoma
MONDO:0006066	acinar prostate adenocarcinoma, foamy gland variant
MONDO:0006067	acinar prostate mucinous adenocarcinoma
MONDO:0006064	lactose intolerance
MONDO:0021680	streptococcal infection
MONDO:0006065	lactose intolerance adult type
MONDO:0006063	carbohydrate metabolic disorder
MONDO:0006060	nasopharyngeal squamous cell carcinoma
MONDO:0006061	cervical artery dissection
MONDO:0021678	gram-negative bacterial infections
MONDO:0018037	hyper-IgE syndrome
MONDO:0021679	gram-positive bacterial infections
MONDO:0018036	immunodeficiency due to absence of thymus
MONDO:0018039	selective IgM deficiency
MONDO:0018038	immunodeficiency with isotype or light chain deficiencies with normal number of B-cells
MONDO:0018033	other immunodeficiency syndromes due to defects in innate immunity
MONDO:0018032	constitutional neutropenia with extra-hematopoietic manifestations
MONDO:0018035	syndrome with combined immunodeficiency
MONDO:0018034	thalidomide embryopathy
MONDO:0021670	post-infectious syndrome
MONDO:0033619	myopathy, epilepsy, and progressive cerebral atrophy
MONDO:0018020	mercury poisoning
MONDO:0033618	Vissers-Bodmer syndrome
MONDO:0021673	post-bacterial disorder
MONDO:0021674	post-viral disorder
MONDO:0033615	coenzyme q10 deficiency, primary, 9
MONDO:0006039	infectious colitis
MONDO:0033614	spastic paraplegia 83, autosomal recessive
MONDO:0033613	neurodevelopmental disorder with progressive spasticity and brain white matter abnormalities
MONDO:0021677	post-infectious neuralgia
MONDO:0006037	hydrolethalus syndrome
MONDO:0006038	indeterminate colitis
MONDO:0008699	achalasia microcephaly syndrome
MONDO:0008698	achalasia
MONDO:0006035	gastric tubular adenocarcinoma
MONDO:0006036	granulosa cell tumor
MONDO:0008697	acetophenetidin sensitivity
MONDO:0006033	diffuse intrinsic pontine glioma
MONDO:0008696	acanthosis nigricans-insulin resistance-muscle cramps-acral enlargement syndrome
MONDO:0006034	gastric adenosquamous carcinoma
MONDO:0008695	chorea-acanthocytosis
MONDO:0006031	chronic rhinosinusitis
MONDO:0008694	pseudoprogeria syndrome
MONDO:0008693	ablepharon macrostomia syndrome
MONDO:0006032	cystitis
MONDO:0008692	abetalipoproteinemia
MONDO:0008691	zinc, elevated plasma
MONDO:0006030	chronic cystitis
MONDO:0008690	xeroderma pigmentosum, autosomal dominant, mild
MONDO:0018029	congenital factor XIII deficiency
MONDO:0018026	tetraploidy syndrome
MONDO:0021667	neuralgia
MONDO:0033622	spermatogenic failure 44
MONDO:0018025	chronic actinic dermatitis
MONDO:0021668	disorder involving pain
MONDO:0033621	spinal muscular atrophy, infantile, James type
MONDO:0021669	post-infectious disorder
MONDO:0018028	tetrasomy 5p
MONDO:0018027	duplication/inversion 15q11
MONDO:0033620	myofibrillar myopathy 10
MONDO:0018022	hemoglobin Lepore-beta-thalassemia syndrome
MONDO:0018021	hypotrichosis-deafness syndrome
MONDO:0018024	hydroa vacciniforme
MONDO:0018023	hemoglobin M disease
MONDO:0021660	deep seated dermatophytosis
MONDO:0021661	coronary atherosclerosis
MONDO:0021662	bile duct neoplasm
MONDO:0021663	sarcomatoid squamous cell carcinoma
MONDO:0021664	cervical aortic arch
MONDO:0021665	Refsum disease
MONDO:0021666	ear infection
MONDO:0006048	pancreatic neuroendocrine tumor
MONDO:0006049	papillary lung adenocarcinoma
MONDO:0006046	ovarian serous cystadenocarcinoma
MONDO:0006047	pancreatic adenocarcinoma
MONDO:0006044	nephrosclerosis
MONDO:0006045	ovarian clear cell adenocarcinoma
MONDO:0006042	meningeal tuberculosis
MONDO:0006043	metaplastic breast carcinoma
MONDO:0006040	lactic acidosis
MONDO:0006041	lung carcinoid tumor
MONDO:0018019	lead poisoning
MONDO:0018018	wild type ATTR amyloidosis
MONDO:0021656	nongerminomatous germ cell tumor
MONDO:0018015	intermittent hydrarthrosis
MONDO:0021657	ovarian sex cord-stromal tumor
MONDO:0018014	transient neonatal multiple acyl-CoA dehydrogenase deficiency
MONDO:0018017	goblet cell carcinoma
MONDO:0021658	vascular ectasia
MONDO:0018016	classic neuroendocrine tumor of appendix
MONDO:0021659	combined carcinoid and adenocarcinoma
MONDO:0033631	combined oxidative phosphorylation deficiency 51
MONDO:0018011	juvenile overlap myositis
MONDO:0033630	neurodevelopmental disorder with speech impairment and dysmorphic facies
MONDO:0018010	juvenile idiopathic inflammatory myopathy
MONDO:0018013	non-immunoglobulin-mediated membranoproliferative glomerulonephritis
MONDO:0018012	tetanus
MONDO:0008719	acrorenal syndrome, autosomal recessive
MONDO:0008718	Morvan syndrome
MONDO:0008717	acromesomelic dysplasia, Hunter-Thompson type
MONDO:0008716	acrogeria
MONDO:0008715	acrofrontofacionasal dysostosis
MONDO:0008714	acrofacial dysostosis Rodriguez type
MONDO:0008713	acrodermatitis enteropathica
MONDO:0008712	acrocraniofacial dysostosis
MONDO:0008711	Goodman syndrome
MONDO:0008710	RAB23-related Carpenter syndrome
MONDO:0008709	acrocephalopolydactyly
MONDO:0008729	congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency
MONDO:0008728	classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency
MONDO:0008727	congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency
MONDO:0008726	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis
MONDO:0008725	congenital lipoid adrenal hyperplasia due to STAR deficency
MONDO:0008724	adducted thumbs-arthrogryposis syndrome, Christian type
MONDO:0008723	very long chain acyl-CoA dehydrogenase deficiency
MONDO:0008722	short chain acyl-CoA dehydrogenase deficiency
MONDO:0008721	medium chain acyl-CoA dehydrogenase deficiency
MONDO:0008720	congenital isolated adrenocorticotropic hormone deficiency
MONDO:0008708	acrocallosal syndrome
MONDO:0008707	acro-renal-mandibular syndrome
MONDO:0008706	Ackerman syndrome
MONDO:0008705	lysosomal acid phosphatase deficiency
MONDO:0008704	short-limb skeletal dysplasia with severe combined immunodeficiency
MONDO:0008703	acromesomelic dysplasia, Grebe type
MONDO:0008702	achondrogenesis type II
MONDO:0008701	achondrogenesis type IA
MONDO:0008700	acheiropody
MONDO:0008759	oxoglutaricaciduria
MONDO:0008758	mitochondrial DNA depletion syndrome 4a
MONDO:0008757	alopecia universalis congenita
MONDO:0008756	alopecia - intellectual disability syndrome
MONDO:0008755	Moynahan syndrome
MONDO:0008754	alopecia - contractures - dwarfism - intellectual disability syndrome
MONDO:0008753	alkaptonuria
MONDO:0008752	Alexander disease
MONDO:0008751	corticosterone methyloxidase type 1 deficiency
MONDO:0008750	microcephaly-albinism-digital anomalies syndrome
MONDO:0021722	vulvodynia
MONDO:0021723	vaginismus
MONDO:0021725	Abderhalden-Kaufmann-Lignac syndrome
MONDO:0021726	abdominal cystic lymphangioma
MONDO:0021727	aberrant subclavian artery
MONDO:0006109	malignant biphasic mesothelioma
MONDO:0006107	benign thyroid gland neoplasm
MONDO:0008769	neuronal ceroid lipofuscinosis 2
MONDO:0006108	bile duct adenoma
MONDO:0008768	neuronal ceroid lipofuscinosis 4A
MONDO:0021720	fetal alcohol spectrum disorders
MONDO:0006105	benign conjunctival neoplasm
MONDO:0008767	neuronal ceroid lipofuscinosis 3
MONDO:0006106	benign smooth muscle neoplasm
MONDO:0006103	benign adrenal gland pheochromocytoma
MONDO:0008766	amaurosis-hypertrichosis syndrome
MONDO:0008765	Leber congenital amaurosis 2
MONDO:0006104	benign carotid body paraganglioma
MONDO:0008764	Leber congenital amaurosis 1
MONDO:0006101	Bartholin gland squamous cell carcinoma
MONDO:0008763	Alstrom syndrome
MONDO:0006102	basaloid carcinoma
MONDO:0008762	autosomal recessive Alport syndrome
MONDO:0008761	alpha-2-deficient collagen disease
MONDO:0006100	Bartholin gland carcinoma
MONDO:0008760	beta-ketothiolase deficiency
MONDO:0021718	polyneuritis
MONDO:0008739	agenesis of cerebral white matter
MONDO:0008738	aganglionosis, total intestinal
MONDO:0008737	congenital afibrinogenemia
MONDO:0008736	peroxisome biogenesis disorder 2B
MONDO:0008735	adrenocortical unresponsiveness to ACTH with postreceptor defect
MONDO:0008734	adrenocortical carcinoma, hereditary
MONDO:0008733	familial glucocorticoid deficiency
MONDO:0008732	adrenal hypoplasia, cytomegalic type
MONDO:0008731	familial adrenal hypoplasia with absent pituitary luteinizing hormone
MONDO:0008730	congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency
MONDO:0021702	alcohol amnestic disorder
MONDO:0008749	pseudohypoparathyroidism type 2
MONDO:0008748	Hermansky-Pudlak syndrome 1
MONDO:0008747	oculocutaneous albinism type 3
MONDO:0008746	oculocutaneous albinism type 2
MONDO:0008745	oculocutaneous albinism type 1A
MONDO:0008744	alar cartilages hypoplasia-coloboma-telecanthus syndrome
MONDO:0008743	Stimmler syndrome
MONDO:0008742	autosomal dominant severe congenital neutropenia
MONDO:0008741	PAGOD syndrome
MONDO:0008740	agnathia-otocephaly complex
MONDO:0043083	coronal synostosis, syndactyly and jejunal atresia
MONDO:0043085	chromosome 1, uniparental disomy 1q12 q21
MONDO:0043087	thickened earlobes with conductive deafness from incus-stapes abnormalities
MONDO:0043089	acute posterior multifocal placoid pigment epitheliopathy
MONDO:0043094	ichthyosis, follicular
MONDO:0043096	holoacardius amorphus
MONDO:0043099	Hordnes Engebretsen Knudtson syndrome
MONDO:0021582	lentigo
MONDO:0021583	melanocytic skin neoplasm
MONDO:0021588	eyelid sebaceous gland carcinoma
MONDO:0021580	neoplasm of jaw
MONDO:0021581	connective tissue neoplasm
MONDO:0021579	neoplasm of femur
MONDO:0033559	intellectual developmental disorder with seizures and language delay
MONDO:0033558	autoinflammation, immune dysregulation, and eosinophilia
MONDO:0033560	mitochondrial complex 1 deficiency, nuclear type 35
MONDO:0033566	combined oxidative phosphorylation deficiency 48
MONDO:0033565	oocyte maturation defect 9
MONDO:0033564	oocyte maturation defect 8
MONDO:0033563	retinitis pigmentosa 90
MONDO:0033562	neurodevelopmental disorder with dysmorphic facies, impaired speech, and hypotonia
MONDO:0033561	deeah syndrome
MONDO:0033569	combined oxidative phosphorylation deficiency 49
MONDO:0033571	skeletal muscle glycogen content and metabolism quantitative trait locus
MONDO:0033570	combined oxidative phosphorylation deficiency 50
MONDO:0033572	intellectual developmental disorder with epilepsy, behavioral abnormalities, and coarse facies
MONDO:0021530	benign neoplasm of subglottis
MONDO:0021531	fibroma of lung
MONDO:0021532	fibroma of prostate
MONDO:0008559	thrombophilia due to thrombin defect
MONDO:0021533	intestinal neuroendocrine tumor G1
MONDO:0008558	autoimmune thrombocytopenic purpura
MONDO:0021534	rectal neuroendocrine tumor G1
MONDO:0008557	Paris-Trousseau thrombocytopenia
MONDO:0008556	thrombocytopenia, cyclic
MONDO:0008555	thrombocytopenia 2
MONDO:0008554	thrombocythemia 1
MONDO:0008553	platelet-type bleeding disorder 17
MONDO:0008552	platelet-type bleeding disorder 16
MONDO:0008551	thoracolaryngopelvic dysplasia
MONDO:0008550	thoracolaryngopelvic dysplasia
MONDO:0021524	benign neoplasm of buccal mucosa
MONDO:0021525	benign neoplasm of corpus uteri
MONDO:0021527	benign neoplasm of meninges
MONDO:0021528	benign neoplasm of male breast
MONDO:0021529	benign neoplasm of chest wall
MONDO:0021520	benign neoplasm of floor of mouth
MONDO:0021521	benign neoplasm of mediastinum
MONDO:0021522	benign neoplasm of lower jaw bone
MONDO:0008569	thyroid hormone resistance, generalized, autosomal dominant
MONDO:0021523	benign neoplasm of pharynx
MONDO:0008568	thyroid hormone plasma membrane transport defect
MONDO:0008567	thyroid cancer, nonmedullary, 1
MONDO:0008566	thyroid cancer, nonmedullary, 2
MONDO:0008565	familial thyroglossal duct cyst
MONDO:0008564	DiGeorge syndrome
MONDO:0008563	thumb stiffness-brachydactyly-intellectual disability syndrome
MONDO:0008562	thumb deformity-alopecia-pigmentation anomaly syndrome
MONDO:0008561	thumb deformity
MONDO:0008560	thrombophilia due to activated protein C resistance
MONDO:0021513	benign neoplasm of tonsil
MONDO:0033534	combined oxidative phosphorylation deficiency 46
MONDO:0021514	benign neoplasm of pericardium
MONDO:0033533	combined oxidative phosphorylation deficiency 45
MONDO:0021515	benign neoplasm of ethmoidal sinus
MONDO:0033532	Suleiman-El-Hattab syndrome
MONDO:0021516	benign neoplasm of glottis
MONDO:0021517	benign neoplasm of trachea
MONDO:0021518	benign neoplasm of hard palate
MONDO:0008539	distal arthrogryposis type 10
MONDO:0008538	temporal arteritis
MONDO:0021510	benign neoplasm of prostate
MONDO:0021511	benign neoplasm of adrenal gland
MONDO:0033537	combined oxidative phosphorylation deficiency 47
MONDO:0008537	telecanthus
MONDO:0021512	benign neoplasm of thymus
MONDO:0008536	temperature-sensitive lethal mutation
MONDO:0008535	telangiectasia, hereditary hemorrhagic, type 1
MONDO:0008534	generalized essential telangiectasia
MONDO:0008533	teeth, supernumerary
MONDO:0008532	teeth present at birth
MONDO:0008531	T-complex locus TCP10B
MONDO:0008530	teeth, odd shapes of
MONDO:0033546	neurodegeneration, infantile-onset, biotin-responsive
MONDO:0021503	benign neoplasm of gallbladder
MONDO:0033545	mitochondrial DNA depletion syndrome 19
MONDO:0033544	Tolchin-Le Caignec syndrome
MONDO:0021505	benign neoplasm of endocardium
MONDO:0033543	cone-rod synaptic disorder syndrome, congenital nonprogressive
MONDO:0021506	benign neoplasm of spinal cord
MONDO:0033542	immunodeficiency 70
MONDO:0021507	benign neoplasm of brain stem
MONDO:0033541	immunodeficiency 69
MONDO:0021508	benign neoplasm of epicardium
MONDO:0021509	benign neoplasm of myocardium
MONDO:0033549	optic atrophy 12
MONDO:0008549	thoracic dysostosis, isolated
MONDO:0033548	myopathy, congenital, with diaphragmatic defects, respiratory insufficiency, and dysmorphic facies
MONDO:0008548	theophylline Biotransformation
MONDO:0021500	benign neoplasm of spleen
MONDO:0008547	thanatophoric dysplasia type 2
MONDO:0033547	Li-Ghorbani-Weisz-Hubshman syndrome
MONDO:0021501	benign neoplasm of small intestine
MONDO:0008546	thanatophoric dysplasia type 1
MONDO:0008545	thalassemia, beta+, silent allele
MONDO:0008544	tetramelic monodactyly
MONDO:0008543	tetralogy of fallot and glaucoma
MONDO:0008542	tetralogy of fallot
MONDO:0008541	spermatic cord torsion
MONDO:0008540	extensor tendons of finger anomalies
MONDO:0033557	hemophagocytic lymphohistiocytosis, familial, 6
MONDO:0033556	muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type b, 15
MONDO:0033555	immunodeficiency 73c with defective neutrophil chemotaxis and hypogammaglobulinemia
MONDO:0033554	immunodeficiency 73b with defective neutrophil chemotaxis and lymphopenia
MONDO:0033552	blood group, lewis system
MONDO:0033551	immunodeficiency 72 with autoinflammation
MONDO:0033550	high density lipoprotein cholesterol level quantitative trait locus 7
MONDO:0021571	multiple sclerosis, susceptibility to 1
MONDO:0021573	oocyte maturation defect 2
MONDO:0021574	oocyte maturation defect 3
MONDO:0021575	oocyte maturation defect 4
MONDO:0021576	fallopian tube endometrioid tumor
MONDO:0021577	malignant mediastinal neural neoplasm
MONDO:0021578	sternal neoplasm
MONDO:0008599	trigeminal neuralgia
MONDO:0008598	trichodysplasia-xeroderma syndrome
MONDO:0008597	trichorhinophalangeal syndrome, type III
MONDO:0008596	trichorhinophalangeal syndrome type I
MONDO:0008595	trichoepitheliomas, multiple desmoplastic
MONDO:0008594	familial multiple discoid fibromas
MONDO:0021570	Hauptmann-Thannhauser muscular dystrophy
MONDO:0008593	trichomegaly
MONDO:0008592	tricho-dento-osseous syndrome
MONDO:0008591	tremor-nystagmus-duodenal ulcer syndrome
MONDO:0008590	tremor, hereditary essential, 1
MONDO:0021568	renal tubule disease
MONDO:0021569	Emery-Dreifuss muscular dystrophy 2, autosomal dominant
MONDO:0021562	omphalitis
MONDO:0021559	non-autoimmune hemolytic anemia
MONDO:0021553	transverse myelitis
MONDO:0008579	toes, relative length of first and second
MONDO:0008578	toe, rotated fifth
MONDO:0008577	toe, misshapen
MONDO:0008576	toe, fifth, number of phalanges 1N
MONDO:0008575	nicotine dependence
MONDO:0008574	Tl antigen
MONDO:0008573	tibial torsion, bilateral medial
MONDO:0008572	tibia, hypoplasia or aplasia of, with polydactyly
MONDO:0008571	Blount disease, infantile
MONDO:0008570	thyrotoxic periodic paralysis, susceptibility to, 1
MONDO:0021546	ependymal tumor of spinal cord
MONDO:0021547	amelogenesis imperfecta type 3B
MONDO:0021548	total early-onset cataract
MONDO:0021540	hamartoma of lung
MONDO:0021541	hemangioma of retina
MONDO:0021542	hemangioma of choroid
MONDO:0021543	hemangioma of gingiva
MONDO:0021545	myomatous neoplasm
MONDO:0008589	tremor of intention, ataxia, and lipofuscinosis
MONDO:0008588	hereditary geniospasm
MONDO:0008587	tracheobronchopathia osteochondroplastica
MONDO:0008586	esophageal atresia/tracheoesophageal fistula
MONDO:0008585	HELLP syndrome
MONDO:0008584	torus palatinus and torus mandibularis
MONDO:0008583	inherited torticollis
MONDO:0008582	tooth and nail syndrome
MONDO:0008581	malposition of teeth with or without hypodontia/oligodontia
MONDO:0008580	toes, space between first and second
MONDO:0021535	pancreatic neuroendocrine tumor G1
MONDO:0021537	undifferentiated carcinoma of nasopharynx
MONDO:0021538	verrucous carcinoma of oral cavity
MONDO:0021539	hamartoma of skin appendage
MONDO:0700084	myopathy caused by varation in GMPPB
MONDO:0700086	uniparental disomy
MONDO:0700085	pentasomy
MONDO:0700088	paroxysmal nonkinesigenic dyskinesia
MONDO:0700087	Usher syndrome type 1B
MONDO:0700089	paroxysmal nonkinesigenic dyskinesia 1
MONDO:0008609	Tristichiasis
MONDO:0008608	Down syndrome
MONDO:0008607	triphalangeal thumbs-brachyectrodactyly syndrome
MONDO:0008606	Say-field-Coldwell syndrome
MONDO:0008605	triphalangeal thumb, Nonopposable
MONDO:0700091	ring chromosome anomaly
MONDO:0008604	triphalangeal thumb with double phalanges
MONDO:0700090	epilepsy, familial temporal lobe, 1
MONDO:0008603	trigonocephaly 1
MONDO:0700092	neurodevelopmental disorder
MONDO:0008602	triglyceride storage disease, type 2
MONDO:0008601	triglyceride storage disease, type 1
MONDO:0008600	trigger thumb
MONDO:0700062	mosaic
MONDO:0700061	mosaic vs complete
MONDO:0700064	aneuploidy
MONDO:0700063	complete
MONDO:0700060	leukemia, acute, X-linked
MONDO:0700069	myopathy caused by varation in POMGNT2
MONDO:0700066	myopathy caused by varation in FKRP
MONDO:0700065	trisomy
MONDO:0700068	myopathy caused by varation in POMGNT1
MONDO:0700067	myopathy caused by varation in FKTN
MONDO:0700075	congenital muscular dystrophy caused by varation in POMGNT2
MONDO:0700071	myopathy caused by varation in POMT2
MONDO:0700070	myopathy caused by varation in POMT1
MONDO:0008639	vascular helix of umbilical cord
MONDO:0008638	varicose disease
MONDO:0008637	bifid uvula
MONDO:0008636	double uterus-hemivagina-renal agenesis syndrome
MONDO:0008635	uterine anomalies
MONDO:0008634	urticaria, familial localized heat
MONDO:0008633	Muckle-Wells syndrome
MONDO:0008632	urticaria, aquagenic
MONDO:0008631	renal agenesis
MONDO:0008630	urinary bladder, atony of
MONDO:0021605	benign eyelid neoplasm
MONDO:0021607	eyelid seborrheic keratosis
MONDO:0008649	venular insufficiency, systemic
MONDO:0008648	ventricular tachycardia, familial
MONDO:0008647	hypertrophic cardiomyopathy 1
MONDO:0008646	long QT syndrome 1
MONDO:0008645	ventricular extrasystoles with syncopal episodes-perodactyly-robin sequence syndrome
MONDO:0008644	velocardiofacial syndrome
MONDO:0008643	veins, pattern of, on anterior thorax
MONDO:0008642	VACTERL/vater association
MONDO:0008641	retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations
MONDO:0008640	vasculitis, lymphocytic, nodular
MONDO:0008619	ulna metaphyseal dysplasia syndrome
MONDO:0008618	mesomelic dwarfism, Reinhardt-Pfeiffer type
MONDO:0008617	inflammatory bowel disease 11
MONDO:0008616	twinning due to superfetation
MONDO:0008615	tune deafness
MONDO:0008614	suppressor of tumorigenicity 3
MONDO:0008613	Tuftsin deficiency
MONDO:0008612	tuberous sclerosis 1
MONDO:0008611	humerus trochlea aplasia
MONDO:0008610	blue color blindness
MONDO:0008629	urolithiasis, uric acid, autosomal dominant
MONDO:0008628	ureterocele
MONDO:0008627	ureter cancer
MONDO:0008626	ureter, bifid or double
MONDO:0008625	urate-binding globulin, decrease 1N
MONDO:0008624	Upington disease
MONDO:0008623	Undritz anomaly
MONDO:0008622	tricho-retino-dento-digital syndrome
MONDO:0008621	uncombable hair syndrome
MONDO:0008620	upper limb mesomelic dysplasia
MONDO:0700007	idiopathic disease
MONDO:0700004	idiopathic vs non-idiopathic
MONDO:0700003	obstetric disorder
MONDO:0700006	non-idiopathic
MONDO:0700005	idiopathic
MONDO:0700000	ALG9-associated autosomal dominant polycystic kidney disease
MONDO:0700002	ATP1A3-associated neurological disorder
MONDO:0700001	shrinking lung syndrome
MONDO:0700057	neurological pain disorder
MONDO:0021494	benign neoplasm of parotid gland
MONDO:0021495	benign neoplasm of sublingual gland
MONDO:0021496	benign neoplasm of lip
MONDO:0021497	benign neoplasm of cerebrum
MONDO:0021498	benign neoplasm of placenta
MONDO:0021499	benign neoplasm of cerebellum
MONDO:0021490	benign neoplasm of sebaceous gland
MONDO:0021491	benign neoplasm of gum
MONDO:0021492	benign neoplasm of major salivary gland
MONDO:0021493	benign neoplasm of minor salivary gland
MONDO:0033483	erythrocytosis, familial, 5
MONDO:0033482	spinocerebellar ataxia 47
MONDO:0033481	spinocerebellar ataxia 46
MONDO:0033480	spinocerebellar ataxia 45
MONDO:0033486	leukodystrophy, hypomyelinating, 14
MONDO:0033485	short-rib thoracic dysplasia 19 with or without polydactyly
MONDO:0021483	benign neoplasm of frontal sinus
MONDO:0021484	benign neoplasm of maxillary sinus
MONDO:0021485	benign neoplasm of iris
MONDO:0021486	benign neoplasm of ciliary body
MONDO:0021487	benign neoplasm of choroid
MONDO:0021488	benign neoplasm of lacrimal gland
MONDO:0021489	benign neoplasm of sweat gland
MONDO:0021480	benign neoplasm of soft palate
MONDO:0021481	benign neoplasm of submandibular gland
MONDO:0021482	benign neoplasm of middle ear
MONDO:0033493	fibromatosis, gingival, 5
MONDO:0033492	Coffin-Siris syndrome 6
MONDO:0021472	benign neoplasm of scrotum
MONDO:0021473	benign neoplasm of epididymis
MONDO:0021474	benign neoplasm of ear
MONDO:0021475	benign neoplasm of nasal cavity
MONDO:0021476	benign neoplasm of tongue
MONDO:0021477	benign neoplasm of sphenoidal sinus
MONDO:0021478	benign neoplasm of nasopharynx
MONDO:0021479	benign neoplasm of oropharynx
MONDO:0008499	short stature-wormian bones-dextrocardia syndrome
MONDO:0008498	strabismus, susceptibility to
MONDO:0008497	Stormorken syndrome
MONDO:0008496	storm syndrome
MONDO:0021470	benign neoplasm of pancreas
MONDO:0021471	benign neoplasm of endometrium
MONDO:0008495	platelet storage pool deficiency
MONDO:0008494	cryohydrocytosis
MONDO:0008493	overhydrated hereditary stomatocytosis
MONDO:0008492	stiff skin syndrome
MONDO:0008491	stiff-person syndrome
MONDO:0008490	otospondylomegaepiphyseal dysplasia, autosomal dominant
MONDO:0021469	benign neoplasm of anus
MONDO:0021461	benign neoplasm of hypopharynx
MONDO:0021462	benign neoplasm of rectum
MONDO:0021463	benign neoplasm of parathyroid gland
MONDO:0021464	benign neoplasm of cecum
MONDO:0021465	benign neoplasm of appendix
MONDO:0021467	benign neoplasm of renal pelvis
MONDO:0021468	benign neoplasm of adrenal medulla
MONDO:0021460	benign neoplasm of salivary gland
MONDO:0021458	benign neoplasm of penis
MONDO:0021459	benign neoplasm of esophagus
MONDO:0033479	spinocerebellar ataxia 44
MONDO:0008439	spastic paraplegia-epilepsy-intellectual disability syndrome
MONDO:0021412	polyp of maxillary sinus
MONDO:0008438	hereditary spastic paraplegia 4
MONDO:0008437	hereditary spastic paraplegia 3A
MONDO:0008436	Sneddon syndrome
MONDO:0008435	Somatomedin, embryonic
MONDO:0008434	Smith-Magenis syndrome
MONDO:0008433	small cell lung carcinoma
MONDO:0008432	ketone compounds, ability to smell
MONDO:0008431	slipped femoral capital epiphyses
MONDO:0008430	skeletal dysplasia with delayed epiphyseal and carpal bone ossification
MONDO:0021404	polyp of sphenoidal sinus
MONDO:0021408	polyp of frontal sinus
MONDO:0021400	polyp of colon
MONDO:0008449	spina bifida
MONDO:0021402	polyp of external auditory canal
MONDO:0008448	spheroid body myopathy
MONDO:0008447	hereditary spherocytosis type 1
MONDO:0008446	sperm protamine P4
MONDO:0008445	delayed speech-facial asymmetry-strabismus-ear lobe creases syndrome
MONDO:0008444	spastic paraplegia, optic atrophy, and dementia
MONDO:0008443	spastic paraplegia-precocious puberty syndrome
MONDO:0008442	spastic paraplegia-neuropathy-poikiloderma syndrome
MONDO:0008441	spastic paraplegia with associated extrapyramidal signs
MONDO:0008440	spastic paraplegia-nephritis-deafness syndrome
MONDO:0008419	scoliosis, isolated, susceptibility to, 1
MONDO:0008418	scleroderma, familial progressive
MONDO:0008417	sclerocornea, autosomal dominant
MONDO:0008416	palmoplantar keratoderma-sclerodactyly syndrome
MONDO:0008415	Scholte syndrome
MONDO:0008414	schizophrenia 1
MONDO:0008413	schizophrenia
MONDO:0008412	intestinal schistosomiasis
MONDO:0008411	ulnar-mammary syndrome
MONDO:0008410	Scheuermann disease
MONDO:0008429	singleton-Merten dysplasia
MONDO:0008428	septooptic dysplasia
MONDO:0008427	sister chromatid exchange, frequency of
MONDO:0008426	Shprintzen-Goldberg syndrome
MONDO:0008425	omphalocele syndrome, Shprintzen-Goldberg type
MONDO:0008424	sella turcica, bridged
MONDO:0008423	sinus node disease and myopia
MONDO:0008422	autosomal dominant sideroblastic anemia
MONDO:0008421	flat face-microstomia-ear anomaly syndrome
MONDO:0008420	seborrheic keratosis
MONDO:0021450	benign neoplasm of heart
MONDO:0021451	benign neoplasm of brain
MONDO:0021452	benign neoplasm of cornea
MONDO:0021453	benign neoplasm of retina
MONDO:0021454	benign neoplasm of eye
MONDO:0021455	benign neoplasm of neck
MONDO:0021456	benign neoplasm of sternum
MONDO:0021457	benign neoplasm of pleura
MONDO:0008479	spondylometaphyseal dysplasia, 'corner fracture' type
MONDO:0008478	spondylometaphyseal dysplasia, Schmidt type
MONDO:0008477	spondylometaphyseal dysplasia, Kozlowski type
MONDO:0008476	spondyloepimetaphyseal dysplasia, Strudwick type
MONDO:0008475	spondylolisthesis
MONDO:0008474	spondyloepiphyseal dysplasia tarda, autosomal dominant
MONDO:0008473	spondyloepimetaphyseal dysplasia, Maroteaux type
MONDO:0008472	spondyloepiphyseal dysplasia, MacDermot type
MONDO:0008471	spondyloepiphyseal dysplasia congenita
MONDO:0008470	spondyloepiphyseal dysplasia with punctate corneal dystrophy
MONDO:0021447	benign neoplasm of testis
MONDO:0021449	benign neoplasm of stomach
MONDO:0021440	benign neoplasm of skin
MONDO:0021441	benign neoplasm of exocrine pancreas
MONDO:0021443	benign neoplasm of lymph node
MONDO:0021444	benign neoplasm of large intestine
MONDO:0021445	benign neoplasm of oral cavity
MONDO:0021446	benign neoplasm of epiglottis
MONDO:0008489	sternum, premature obliteration of sutures of
MONDO:0008488	holoprosencephaly-radial heart renal anomalies syndrome
MONDO:0008487	polycystic ovary syndrome
MONDO:0008486	steatocystoma multiplex-natal teeth syndrome
MONDO:0008485	sebocystomatosis
MONDO:0008484	stapes ankylosis with broad thumbs and toes
MONDO:0008483	stuttering, familial persistent, 1
MONDO:0008482	Sprengel deformity
MONDO:0008481	spondylosis, cervical
MONDO:0008480	odontochondrodysplasia
MONDO:0021437	lipoma of stomach
MONDO:0021439	benign neoplasm of pituitary gland
MONDO:0021431	squamous cell carcinoma of buccal mucosa
MONDO:0008459	spinocerebellar atrophy with pupillary paralysis
MONDO:0008458	spinocerebellar ataxia type 2
MONDO:0008457	spinocerebellar ataxia type 6
MONDO:0008456	spinocerebellar ataxia with rigidity and peripheral neuropathy
MONDO:0008455	spinal muscular atrophy, segmental
MONDO:0008454	spinal intradural arachnoid cysts
MONDO:0008453	adult-onset proximal spinal muscular atrophy, autosomal dominant
MONDO:0008452	spinal muscular atrophy, facioscapulohumeral type
MONDO:0008451	neuronopathy, distal hereditary motor, type 1
MONDO:0008450	spinal arachnoiditis
MONDO:0021427	squamous cell carcinoma of lip
MONDO:0021429	squamous cell carcinoma of floor of mouth
MONDO:0021420	polyp of vocal cord
MONDO:0021421	carcinoid tumors, intestina
MONDO:0021424	hemangiopericytoma of skin
MONDO:0008469	spondyloepimetaphyseal dysplasia-hypotrichosis syndrome
MONDO:0008468	spondyloarthropathy, susceptibility to, 2
MONDO:0008467	Czeizel-Losonci syndrome
MONDO:0008466	Karsch-Neugebauer syndrome
MONDO:0008465	Patterson-Stevenson-Fontaine syndrome
MONDO:0008464	split hand-foot malformation 1
MONDO:0008463	split-hand and split-foot with hypodontia
MONDO:0008462	split lower lip
MONDO:0008461	splenomegaly syndrome with splenic Germinal center hypoplasia and reduced circulating T helper cells
MONDO:0008460	splenogonadal fusion-limb defects-micrognathia syndrome
MONDO:0021416	polyp of gallbladder
MONDO:0021418	polyp of ethmoidal sinus
MONDO:0008519	multiple synostoses syndrome 1
MONDO:0008518	calcaneonavicular coalition
MONDO:0008517	syndactyly-polydactyly-ear lobe syndrome
MONDO:0008516	syndactyly type 5
MONDO:0008515	syndactyly type 4
MONDO:0008514	syndactyly type 3
MONDO:0008513	synpolydactyly type 1
MONDO:0008512	syndactyly type 1
MONDO:0008511	proximal symphalangism
MONDO:0008510	symphalangism with multiple anomalies of hands and feet
MONDO:0008529	T-cell Subgroups, non-HLA-linked
MONDO:0008528	tear protein, anodal
MONDO:0008527	tarsal coalition
MONDO:0008526	talonavicular coalition
MONDO:0008525	syringomyelia, isolated
MONDO:0008524	syringomas, multiple
MONDO:0008523	Blau syndrome
MONDO:0008522	synovial chondromatosis, familial, with dwarfism
MONDO:0008521	tarsal-carpal coalition syndrome
MONDO:0008520	brachydactyly-elbow wrist dysplasia syndrome
MONDO:0008509	distal symphalangism
MONDO:0008508	symphalangism, C. S. Lewis type
MONDO:0008507	surface polypeptides, anonymous
MONDO:0008506	symphalangism of toes
MONDO:0008505	surface antigen, glycoprotein 75
MONDO:0008504	supravalvular aortic stenosis
MONDO:0008503	Worster-Drought syndrome
MONDO:0008502	sulfhemoglobinemia, congenital
MONDO:0008501	Sturge-Weber syndrome
MONDO:0008500	striae distensae, familial
MONDO:0021373	neoplasm of parietal lobe
MONDO:0021374	neoplasm of cerebral hemisphere
MONDO:0021375	tumor of duodenum
MONDO:0021377	hypertrophic lichen planus
MONDO:0021378	neoplasm of endocardium
MONDO:0021379	neoplasm of epicardium
MONDO:0008399	sarcoidosis, susceptibility to, 1
MONDO:0021370	neoplasm of minor salivary gland
MONDO:0008398	salivary substance, Clostridium botulinum type
MONDO:0008397	aplasia of lacrimal and salivary glands
MONDO:0008396	oculodental syndrome, Rutherfurd type
MONDO:0021372	neoplasm of temporal lobe
MONDO:0033362	developmental and epileptic encephalopathy, 53
MONDO:0008395	Ruvalcaba syndrome
MONDO:0033361	developmental and epileptic encephalopathy, 52
MONDO:0008394	Silver-Russell syndrome
MONDO:0008393	Rubinstein-Taybi syndrome due to CREBBP mutations
MONDO:0008392	Roussy-Levy syndrome
MONDO:0008391	Robinow-Sorauf syndrome
MONDO:0008390	Rombo syndrome
MONDO:0033369	developmental and epileptic encephalopathy, 60
MONDO:0033368	developmental and epileptic encephalopathy, 59
MONDO:0033367	developmental and epileptic encephalopathy, 58
MONDO:0033366	developmental and epileptic encephalopathy, 57
MONDO:0033365	developmental and epileptic encephalopathy, 56
MONDO:0033364	developmental and epileptic encephalopathy, 55
MONDO:0033363	developmental and epileptic encephalopathy, 54
MONDO:0021364	neoplasm of oropharynx
MONDO:0021366	neoplasm of middle ear
MONDO:0021367	leukemia, myeloid, accelerated-phase
MONDO:0021368	neoplasm of major salivary gland
MONDO:0021360	tumor of parathyroid gland
MONDO:0033373	developmental and epileptic encephalopathy, 64
MONDO:0033372	developmental and epileptic encephalopathy, 63
MONDO:0033371	developmental and epileptic encephalopathy, 62
MONDO:0033370	developmental and epileptic encephalopathy, 61
MONDO:0033375	orofaciodigital syndrome 17
MONDO:0033374	developmental and epileptic encephalopathy, 65
MONDO:0021351	neoplasm of neck
MONDO:0021353	tumor of uterus
MONDO:0021354	tumor of adipose tissue
MONDO:0021355	neoplasm of esophagus
MONDO:0021357	tumor of salivary gland
MONDO:0021358	neoplasm of hypopharynx
MONDO:0008379	retinitis pigmentosa 10
MONDO:0008378	retinitis pigmentosa 9
MONDO:0008377	retinitis pigmentosa 1
MONDO:0008376	retinal venous beading
MONDO:0008375	retinal detachment
MONDO:0021350	neoplasm of thorax
MONDO:0008374	retinal cone dystrophy type 1
MONDO:0008373	retinal arterial tortuosity
MONDO:0008372	retinal aplasia
MONDO:0008371	Dowling-Degos disease
MONDO:0008370	reticular dystrophy of retinal pigment epithelium
MONDO:0021348	neoplasm of testis
MONDO:0021340	intertrigo
MONDO:0021343	carcinoma of floor of mouth
MONDO:0021345	carcinoma of pharynx
MONDO:0008389	autosomal dominant Robinow syndrome
MONDO:0008388	ringed hair disease
MONDO:0008387	ring dermoid of cornea
MONDO:0008386	Axenfeld-Rieger syndrome type 1
MONDO:0008385	rhiny
MONDO:0008384	rheumatoid nodulosis
MONDO:0008383	rheumatoid arthritis
MONDO:0008382	retinoschisis, autosomal dominant
MONDO:0008381	dominant pericentral pigmentary retinopathy
MONDO:0008380	retinoblastoma
MONDO:0021337	tonsil carcinoma
MONDO:0021339	carcinoma of hard palate
MONDO:0021396	polyp of vulva
MONDO:0021398	polyp of rectum
MONDO:0021390	polyp of ureter
MONDO:0021392	polyp of large intestine
MONDO:0021394	polyp of vagina
MONDO:0021385	extrahepatic bile duct neoplasm
MONDO:0021386	neoplasm of mediastinum
MONDO:0021388	neoplasm of chest wall
MONDO:0021389	neoplasm of aortic body
MONDO:0021380	neoplasm of myocardium
MONDO:0021381	neoplasm of pericardium
MONDO:0021383	neoplasm of floor of mouth
MONDO:0033352	neuropathy, congenital hypomelinating
MONDO:0008319	protoporphyria, erythropoietic, 1
MONDO:0008318	Proteus syndrome
MONDO:0008317	proteolytic capacity of plasma
MONDO:0008316	thrombophilia due to protein C deficiency, autosomal dominant
MONDO:0008315	prostate cancer
MONDO:0011967	heterotopia, periventricular, associated with chromosome 5P anomalies
MONDO:0011968	autosomal recessive limb-girdle muscular dystrophy type 2D
MONDO:0008314	pronation-supination of the forearm, impairment of
MONDO:0011965	familial temporal lobe epilepsy 2
MONDO:0008313	pelvic organ prolapse, susceptibility to
MONDO:0008312	autosomal dominant prognathism
MONDO:0011966	periventricular heterotopia with microcephaly, autosomal recessive
MONDO:0008311	progeria-short stature-pigmented nevi syndrome
MONDO:0008310	Hutchinson-Gilford progeria syndrome
MONDO:0011969	ALG8-CDG
MONDO:0011970	rolandic epilepsy-paroxysmal exercise-induced dystonia-writer's cramp syndrome
MONDO:0011971	hyper-IgM syndrome type 5
MONDO:0011974	retinitis pigmentosa 7
MONDO:0011975	paternal uniparental disomy of chromosome 14
MONDO:0011972	ovarian hyperstimulation syndrome
MONDO:0011973	zinc deficiency, transient neonatal
MONDO:0008329	autosomal dominant pseudohypoaldosteronism type 1
MONDO:0008328	glaucoma 1, open angle, P
MONDO:0008327	exfoliation syndrome
MONDO:0011956	autism, susceptibility to, 3
MONDO:0008326	pseudocholinesterase, increase in plasma level of
MONDO:0008325	Pseudoatrophoderma colli
MONDO:0011957	retinal macular dystrophy type 2
MONDO:0011954	melanoma, cutaneous malignant, susceptibility to, 4
MONDO:0008324	pseudoarthrogryposis
MONDO:0008323	Liddle syndrome
MONDO:0011955	diabetes mellitus, noninsulin-dependent, 4
MONDO:0008322	pseudoachondroplasia
MONDO:0008321	pruritus, hereditary localized
MONDO:0008320	Protrusio acetabuli
MONDO:0011958	bile and pancreatic ducts, complete absence of
MONDO:0011959	sweet syndrome
MONDO:0011960	schizophrenia 11
MONDO:0011963	Joubert syndrome 2
MONDO:0011964	DPAGT1-CDG
MONDO:0011961	hereditary sensory and autonomic neuropathy type 1B
MONDO:0011962	endometrial cancer
MONDO:0011945	Gaucher disease perinatal lethal
MONDO:0011946	diaphanospondylodysostosis
MONDO:0011943	systemic lupus erythematosus with nephritis, susceptibility to, 2
MONDO:0011944	systemic lupus erythematosus with nephritis, susceptibility to, 3
MONDO:0011949	Thai symphalangism syndrome
MONDO:0011947	HNP1
MONDO:0011948	pontocerebellar hypoplasia type 3
MONDO:0011952	amyotrophic lateral sclerosis type 7
MONDO:0011953	familial acute necrotizing encephalopathy
MONDO:0011950	infantile-onset autosomal recessive nonprogressive cerebellar ataxia
MONDO:0011951	amyotrophic lateral sclerosis type 6
MONDO:0033304	nonsyndromic deafness, Y-linked
MONDO:0008309	primary release disorder of platelets
MONDO:0033309	Joubert syndrome 32
MONDO:0033308	Joubert syndrome 30
MONDO:0008308	priapism, familial idiopathic
MONDO:0008307	presenile dementia, Kraepelin type
MONDO:0008306	ABri amyloidosis
MONDO:0008305	Currarino triad
MONDO:0008304	premature chromatid separation trait
MONDO:0011934	dermatofibrosarcoma protuberans
MONDO:0008303	familial male-limited precocious puberty
MONDO:0011935	retinitis pigmentosa 30
MONDO:0008302	centra precocious puberty 1
MONDO:0011932	hypotrichosis 6
MONDO:0011933	ALG2-CDG
MONDO:0008301	Guttmacher syndrome
MONDO:0011938	atrial septal defect 2
MONDO:0008300	Prader-Willi syndrome
MONDO:0011939	Spondyloenchondrodysplasia with immune dysregulation
MONDO:0011936	microphthalmia with brain and digit anomalies
MONDO:0011937	peeling skin syndrome 4
MONDO:0011941	mycobacterium tuberculosis, susceptibility to, 1
MONDO:0011942	systemic lupus erythematosus with nephritis, susceptibility to, 1
MONDO:0011940	mycobacterium tuberculosis, susceptibility to
MONDO:0033312	schizophrenia 19
MONDO:0033311	Joubert syndrome 33
MONDO:0033310	Joubert syndrome 31
MONDO:0021331	carcinoma of parotid gland
MONDO:0021333	carcinoma of lip
MONDO:0021334	immunoproliferative disorder
MONDO:0021335	carcinoma of duodenum
MONDO:0008359	radio-renal syndrome
MONDO:0008358	radial ray hypoplasia-choanal atresia syndrome
MONDO:0008357	radial hypoplasia-triphalangeal thumbs-hypospadias-maxillary diastema syndrome
MONDO:0008356	radial heads, posterior dislocation of
MONDO:0008355	pyloric stenosis, infantile hypertrophic, 1
MONDO:0008354	purpura simplex
MONDO:0008353	pruritic urticarial papules and plaques of pregnancy
MONDO:0008352	pupillary membrane, persistence of
MONDO:0008351	pupil, egg-shaped
MONDO:0008350	pulmonic stenosis and deafness
MONDO:0021326	malignant neoplasm of cervical esophagus
MONDO:0021327	carcinoma of urethra
MONDO:0021329	carcinoma of soft palate
MONDO:0021320	malignant tumor of floor of mouth
MONDO:0021321	malignant tumor of extrahepatic bile duct
MONDO:0021322	malignant tumor of meninges
MONDO:0021323	malignant neoplasm of chest wall
MONDO:0021324	malignant neoplasm of abdominal esophagus
MONDO:0021325	malignant neoplasm of thoracic esophagus
MONDO:0008369	proximal renal tubular acidosis
MONDO:0008368	autosomal dominant distal renal tubular acidosis
MONDO:0011998	autosomal dominant slowed nerve conduction velocity
MONDO:0008367	red cell phospholipid defect with hemolysis
MONDO:0011999	otosclerosis 3
MONDO:0008366	red cell permeability defect
MONDO:0008365	recombinant 8 syndrome
MONDO:0008364	Raynaud disease
MONDO:0008363	raindrop hypopigmentation
MONDO:0008362	ragweed sensitivity
MONDO:0008361	radius, aplasia of, with cleft lip/palate
MONDO:0008360	radioulnar synostosis
MONDO:0021315	malignant tumor of nasopharynx
MONDO:0021316	malignant tumor of minor salivary gland
MONDO:0021317	cancer of cerebellum
MONDO:0021310	malignant tumor of neck
MONDO:0021311	malignant tumor of parathyroid gland
MONDO:0021312	malignant tumor of adrenal cortex
MONDO:0008339	antecubital pterygium syndrome
MONDO:0021313	eyelid cancer
MONDO:0008338	contractures, pterygia, and spondylocarpotarsal fusion syndrome 1A
MONDO:0011989	leishmaniasis
MONDO:0008337	familial pterygium of the conjunctiva
MONDO:0008336	pterygium colli, isolated
MONDO:0011987	cone-rod dystrophy 13
MONDO:0008335	short stature-craniofacial anomalies-genital hypoplasia syndrome
MONDO:0011988	neutrophil immunodeficiency syndrome
MONDO:0008334	psoriasis 1, susceptibility to
MONDO:0008333	pseudoxanthoma elasticum, forme fruste
MONDO:0008332	pseudo-von Willebrand disease
MONDO:0008331	pseudopapilledema
MONDO:0008330	pseudomonilethrix
MONDO:0011992	hereditary spastic paraplegia 25
MONDO:0011993	aspirin resistance
MONDO:0011990	seizures, benign familial neonatal, 3
MONDO:0011991	autosomal recessive nonsyndromic deafness 38
MONDO:0011996	chronic myelogenous leukemia, BCR-ABL1 positive
MONDO:0011997	Hermansky-Pudlak syndrome 2
MONDO:0011994	autosomal dominant nonsyndromic deafness 41
MONDO:0011995	cataract - congenital heart disease - neural tube defect syndrome
MONDO:0021309	malignant neoplasm of endocervix
MONDO:0021300	adenoid cystic carcinoma of oropharynx
MONDO:0021301	adenoma of nipple
MONDO:0021303	adenoma of small intestine
MONDO:0008349	pulmonic stenosis, atrial septal defect, and unique electrocardiographic abnormalities
MONDO:0008348	pulmonary nodular lymphoid hyperplasia
MONDO:0011978	CoQ-responsive OXPHOS deficiency
MONDO:0008347	idiopathic and/or familial pulmonary arterial hypertension
MONDO:0011979	adult-onset foveomacular vitelliform dystrophy
MONDO:0008346	pulmonary hemosiderosis
MONDO:0011976	lipodystrophy-intellectual disability-deafness syndrome
MONDO:0008345	idiopathic pulmonary fibrosis
MONDO:0011977	8q22.1 microdeletion syndrome
MONDO:0008344	pulmonary edema of mountaineers, susceptibility to
MONDO:0008343	pulmonary atresia with ventricular septal defect
MONDO:0008342	pubic bone dysplasia
MONDO:0008341	ptosis-strabismus-ectopic pupils syndrome
MONDO:0011981	autoimmune thyroid disease, susceptibility to, 2
MONDO:0008340	congenital ptosis
MONDO:0011982	autoimmune thyroid disease, susceptibility to, 3
MONDO:0011980	autoimmune thyroid disease, susceptibility to, 1
MONDO:0011985	hyper-IgM syndrome type 4
MONDO:0011986	tropical pancreatitis
MONDO:0011983	autoimmune thyroid disease, susceptibility to, 4
MONDO:0011984	synpolydactyly type 2
MONDO:0008409	MYH7-related late-onset scapuloperoneal muscular dystrophy
MONDO:0008408	scapuloperoneal spinal muscular atrophy, autosomal dominant
MONDO:0008407	neurogenic scapuloperoneal syndrome, Kaeser type
MONDO:0008406	autosomal recessive Emery-Dreifuss muscular dystrophy
MONDO:0008405	scapula, contour of vertebral border of
MONDO:0008404	scalp-ear-nipple syndrome
MONDO:0008403	scalp defects-postaxial polydactyly syndrome
MONDO:0008402	cleft palate-large ears-small head syndrome
MONDO:0008401	pleomorphic adenoma
MONDO:0008400	salivary duct calculi
MONDO:0004713	lower gum cancer
MONDO:0004712	herpes simplex dermatitis
MONDO:0004715	liver carcinoma in situ
MONDO:0004714	atrophic muscular disease
MONDO:0004711	amyloidosis
MONDO:0004710	uterus carcinoma in situ
MONDO:0016702	oligoastrocytoma
MONDO:0016703	anaplastic oligoastrocytoma
MONDO:0016704	glial tumor of neuroepithelial tissue with unknown origin
MONDO:0016705	angiocentric glioma
MONDO:0016700	anaplastic ependymoma
MONDO:0016701	oligoastrocytic tumor
MONDO:0004709	occipital lobe neoplasm
MONDO:0004706	discoid lupus erythematosus of eyelid
MONDO:0004705	liver solitary fibrous tumor
MONDO:0004708	esophagus carcinoma in situ
MONDO:0004707	anal canal carcinoma in situ
MONDO:0004724	submandibular gland cancer
MONDO:0004723	liver leiomyoma
MONDO:0004726	liver inflammatory myofibroblastic tumor
MONDO:0004725	rectum carcinoma in situ
MONDO:0004720	variola minor infection
MONDO:0004722	Wiskott-Aldrich syndrome
MONDO:0004721	liver neoplasm
MONDO:0004717	peliosis hepatis
MONDO:0004716	stomach carcinoma in situ
MONDO:0004719	hard palate cancer
MONDO:0004718	xeroderma of eyelid
MONDO:0004702	uterine cervix leukoplakia
MONDO:0004701	uterine polyp
MONDO:0004704	peroxisomal disease
MONDO:0004703	bladder carcinoma in situ
MONDO:0004700	parotid gland cancer
MONDO:0014093	retinitis pigmentosa 66
MONDO:0014092	schizophrenia 18
MONDO:0014091	mitochondrial complex V (ATP synthase) deficiency nuclear type 4
MONDO:0014090	polydactyly, postaxial, type A6
MONDO:0014097	congenital short bowel syndrome
MONDO:0014096	microcephaly-intellectual disability-phalangeal and neurological anomalies syndrome
MONDO:0014095	dilated cardiomyopathy 1JJ
MONDO:0014094	severe congenital hypochromic anemia with ringed sideroblasts
MONDO:0014099	nephrotic syndrome, type 8
MONDO:0014098	CIDEC-related familial partial lipodystrophy
MONDO:0002178	placenta cancer
MONDO:0002179	placental choriocarcinoma
MONDO:0002174	preretinal fibrosis
MONDO:0002175	degeneration of macula and posterior pole
MONDO:0002176	connective tissue cancer
MONDO:0002177	hyperinsulinism
MONDO:0002170	chronic eustachian salpingitis
MONDO:0002171	giant cell tumor
MONDO:0002172	otosalpingitis
MONDO:0002173	neuroma
MONDO:0014169	dyschromatosis universalis hereditaria 3
MONDO:0014168	severe combined immunodeficiency due to CORO1A deficiency
MONDO:0041775	intraoperative floppy iris syndrome
MONDO:0014163	left ventricular noncompaction 10
MONDO:0014162	infantile hypertrophic cardiomyopathy due to MRPL44 deficiency
MONDO:0014161	vesicoureteral reflux 7
MONDO:0014160	TCR-alpha-beta-positive T-cell deficiency
MONDO:0014167	epilepsy, familial adult myoclonic, 5
MONDO:0014166	paroxysmal nocturnal hemoglobinuria 2
MONDO:0014165	multiple congenital anomalies-hypotonia-seizures syndrome 3
MONDO:0014164	Meckel syndrome, type 11
MONDO:0002189	nodular hidradenoma
MONDO:0002185	hyperostosis
MONDO:0002186	acute maxillary sinusitis
MONDO:0002187	vulvar disease
MONDO:0002188	vulvar nodular hidradenoma
MONDO:0002181	exostosis
MONDO:0002182	communication disorder
MONDO:0002183	enthesopathy
MONDO:0002184	drug-induced hepatitis
MONDO:0014159	autosomal recessive spinocerebellar ataxia 14
MONDO:0014158	nephronophthisis 16
MONDO:0014157	mandibular hypoplasia-deafness-progeroid syndrome
MONDO:0002180	gestational choriocarcinoma
MONDO:0014152	left ventricular noncompaction 8
MONDO:0014151	pulmonary hypertension, neonatal, susceptibility to
MONDO:0014150	childhood onset epileptic encephalopathy
MONDO:0014156	atrial fibrillation, familial, 14
MONDO:0014155	atrial fibrillation, familial, 13
MONDO:0014154	Charcot-Marie-Tooth disease recessive intermediate C
MONDO:0014153	cone-rod dystrophy 18
MONDO:0002156	fallopian tube disease
MONDO:0002157	fallopian tube carcinoma
MONDO:0002158	fallopian tube cancer
MONDO:0002159	fallopian tube leiomyosarcoma
MONDO:0002152	intermittent squint
MONDO:0002153	telogen effluvium
MONDO:0002154	trichomoniasis
MONDO:0002155	cholecystitis
MONDO:0002150	hypothalamic disease
MONDO:0002151	dysostosis
MONDO:0014149	fetal akinesia-cerebral and retinal hemorrhage syndrome
MONDO:0014148	estrogen resistance syndrome
MONDO:0014147	neuronal ceroid lipofuscinosis 13
MONDO:0014146	autosomal dominant hypocalcemia 2
MONDO:0014141	muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B14
MONDO:0014140	muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A14
MONDO:0014145	Leber congenital amaurosis 17
MONDO:0014144	autosomal recessive limb-girdle muscular dystrophy type 2S
MONDO:0014143	Noonan syndrome 8
MONDO:0014142	autosomal recessive limb-girdle muscular dystrophy type 2T
MONDO:0002167	rectum malignant melanoma
MONDO:0002168	rectum sarcoma
MONDO:0002169	rectum adenocarcinoma
MONDO:0002163	thymus lipoma
MONDO:0002164	focal chorioretinitis
MONDO:0002165	rectal neoplasm
MONDO:0002166	rectum lymphoma
MONDO:0002160	cerebral palsy
MONDO:0002161	fallopian tube carcinosarcoma
MONDO:0002162	fallopian tube adenosarcoma
MONDO:0014138	nemaline myopathy 8
MONDO:0014137	precocious puberty, central, 2
MONDO:0014136	pulmonary hypertension, primary, 4
MONDO:0014135	pulmonary hypertension, primary, 3
MONDO:0016797	multiple mitochondrial DNA deletion syndrome
MONDO:0016798	ataxia neuropathy spectrum
MONDO:0016799	mitochondrial oxidative phosphorylation disorder with no known mechanism
MONDO:0014139	Ehlers-Danlos syndrome, progeroid type, 2
MONDO:0016793	mitochondrial oxidative phosphorylation disorder due to a point mutation of mitochondrial DNA
MONDO:0014130	Dowling-Degos disease 2
MONDO:0016794	maternally-inherited mitochondrial myopathy
MONDO:0016795	mitochondrial oxidative phosphorylation disorder due to a duplication of mitochondrial DNA
MONDO:0016796	mitochondrial DNA depletion syndrome, encephalomyopathic form
MONDO:0014134	pulmonary hypertension, primary, 2
MONDO:0014133	developmental and epileptic encephalopathy, 16
MONDO:0016790	tricarboxylic acid cycle disorder
MONDO:0014132	multiple mitochondrial dysfunctions syndrome 3
MONDO:0016791	mitochondrial oxidative phosphorylation disorder due to mitochondrial DNA anomalies
MONDO:0016792	mitochondrial oxidative phosphorylation disorder due to a large-scale single deletion of mitochondrial DNA
MONDO:0014131	hypohidrosis-enamel hypoplasia-palmoplantar keratoderma-intellectual disability syndrome
MONDO:0014192	primary ciliary dyskinesia 22
MONDO:0014191	catecholaminergic polymorphic ventricular tachycardia 5
MONDO:0014190	combined oxidative phosphorylation defect type 17
MONDO:0041751	multibacillary leprosy
MONDO:0041752	paucibacillary leprosy
MONDO:0014196	Hartsfield-Bixler-Demyer syndrome
MONDO:0014195	microcornea-myopic chorioretinal atrophy
MONDO:0014194	mitochondrial complex III deficiency nuclear type 6
MONDO:0014193	primary ciliary dyskinesia 23
MONDO:0014199	developmental and epileptic encephalopathy, 17
MONDO:0014198	mitochondrial DNA depletion syndrome 13
MONDO:0014197	combined immunodeficiency due to MALT1 deficiency
MONDO:0014181	amyotrophic lateral sclerosis type 20
MONDO:0014180	epidermolysis bullosa simplex due to BP230 deficiency
MONDO:0002196	perinatal intestinal perforation
MONDO:0002197	minor vestibular glands adenoma
MONDO:0002198	vulvar glandular neoplasm
MONDO:0002199	benign mixed tumor of the vulva
MONDO:0002192	vulvar angiokeratoma
MONDO:0002193	Bartholin gland benign neoplasm
MONDO:0002194	vestibular papilloma
MONDO:0002195	vulvar squamous neoplasm
MONDO:0002190	vulvar syringoma
MONDO:0002191	syringoma
MONDO:0041755	twin reversal arterial perfusion syndrome
MONDO:0014185	chromosome 3q13.31 deletion syndrome
MONDO:0014184	specific language impairment 5
MONDO:0014183	myopia 23, autosomal recessive
MONDO:0014182	autosomal recessive nonsyndromic deafness 88
MONDO:0014189	age related macular degeneration 13
MONDO:0014187	aortic aneurysm, familial thoracic 8
MONDO:0014186	retinitis pigmentosa with or without situs inversus
MONDO:0014170	complex cortical dysplasia with other brain malformations 3
MONDO:0014179	inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 3
MONDO:0014174	renal-hepatic-pancreatic dysplasia 2
MONDO:0014173	microcephaly 11, primary, autosomal recessive
MONDO:0014172	spermatogenic failure 12
MONDO:0014171	complex cortical dysplasia with other brain malformations 4
MONDO:0014178	inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 2
MONDO:0014177	myopia 22, autosomal dominant
MONDO:0014176	hypotonia, infantile, with psychomotor retardation and characteristic facies
MONDO:0014175	mitochondrial DNA depletion syndrome 12B (cardiomyopathic type), autosomal recessive
MONDO:0004757	chronic ethmoidal sinusitis
MONDO:0004756	nasal cavity neoplasm
MONDO:0004759	bestiality
MONDO:0004758	scotoma
MONDO:0004753	mechanical strabismus
MONDO:0004752	neurofibroma of the heart
MONDO:0004755	monieziasis
MONDO:0004754	rectal prolapse
MONDO:0004751	disease of orbital part of eye adnexa
MONDO:0004750	language disorder
MONDO:0016739	yolk sac tumor of central nervous system
MONDO:0016746	meningeal melanocytoma
MONDO:0016747	primary melanoma of the central nervous system
MONDO:0016748	hemangioblastoma
MONDO:0016749	tumor of cranial and spinal nerves
MONDO:0016742	mixed germ cell tumor of central nervous system
MONDO:0016743	tumor of meninges
MONDO:0016744	primary melanocytic tumor of central nervous system
MONDO:0016745	diffuse leptomeningeal melanocytosis
MONDO:0016740	choriocarcinoma of the central nervous system
MONDO:0016741	teratoma of the central nervous system
MONDO:0004749	myocardium cancer
MONDO:0002105	toxic megacolon
MONDO:0004768	keratoconjunctivitis
MONDO:0004767	vesiculitis
MONDO:0002106	labyrinthine unilateral reactive loss
MONDO:0002107	unilateral hyperactive labyrinth
MONDO:0002108	thyroid cancer
MONDO:0004769	orbital plasma cell granuloma
MONDO:0004764	fibular collateral ligament bursitis
MONDO:0002101	facial nerve neoplasm
MONDO:0002102	cheilitis
MONDO:0004763	carotid artery dissection
MONDO:0002103	factitious disorder
MONDO:0004766	status asthmaticus
MONDO:0002104	conversion disorder
MONDO:0004765	intrinsic asthma
MONDO:0004760	urethral false passage
MONDO:0004762	Taylor syndrome
MONDO:0004761	urethral diverticulum
MONDO:0002100	cardiovascular cancer
MONDO:0016728	cerebellar liponeurocytoma
MONDO:0016729	mixed neuronal-glial tumor
MONDO:0016735	papillary glioneuronal tumor
MONDO:0016736	rosette-forming glioneuronal tumor of fourth ventricule
MONDO:0016737	ganglioneuroma
MONDO:0016738	primary germ cell tumor of central nervous system
MONDO:0016731	desmoplastic infantile astrocytoma/ganglioglioma
MONDO:0016732	dysembryoplastic neuroepithelial tumor
MONDO:0016733	ganglioglioma
MONDO:0016734	anaplastic ganglioglioma
MONDO:0016730	gangliocytoma
MONDO:0004735	Alagille syndrome
MONDO:0004734	erythromelalgia
MONDO:0004737	homocystinuria
MONDO:0004736	inherited amino acid metabolic disorder
MONDO:0004731	central sleep apnea syndrome
MONDO:0004730	speech disorder
MONDO:0004733	pyriform sinus cancer
MONDO:0004732	kidney carcinoma in situ
MONDO:0016717	choroid plexus neoplasm
MONDO:0016718	choroid plexus carcinoma
MONDO:0016719	microcephaly-seizures-intellectual disability-heart disease syndrome
MONDO:0016724	papillary tumor of the pineal region
MONDO:0016725	pineal parenchymal tumor of intermediate differenciation
MONDO:0016726	neuronal tumor
MONDO:0016727	extraventricular neurocytoma
MONDO:0016720	atypical papilloma of choroid plexus
MONDO:0016721	pineal tumor of neuroepithelial tissue
MONDO:0016722	pineoblastoma
MONDO:0016723	pineocytoma
MONDO:0004728	diabetic macular edema
MONDO:0004727	vestibule of mouth cancer
MONDO:0004729	dyskinesia of esophagus
MONDO:0004746	myopathy of extraocular muscle
MONDO:0004745	priapism
MONDO:0004748	lip disease
MONDO:0004747	cleft lip
MONDO:0004742	primary cerebellar degeneration
MONDO:0004741	tyrosinemia
MONDO:0004744	borderline glaucoma
MONDO:0004743	hyperhomocysteinemia
MONDO:0004740	hyperlysinemia
MONDO:0016706	chordoid glioma of the third ventricle
MONDO:0016707	astroblastoma
MONDO:0016708	embryonal tumor of neuroepithelial tissue
MONDO:0016709	anaplastic/large cell medulloblastoma
MONDO:0016713	central nervous system Ewing sarcoma/peripheral primitive neuroectodermal tumor
MONDO:0016714	ganglioneuroblastoma
MONDO:0016715	ependymoblastoma
MONDO:0016716	medulloepithelioma of the central nervous system
MONDO:0016710	medulloblastoma with extensive nodularity
MONDO:0016711	desmoplastic/nodular medulloblastoma
MONDO:0016712	classic medulloblastoma
MONDO:0004739	urea cycle disorder
MONDO:0004738	histidine metabolism disease
MONDO:0002138	allergic contact dermatitis of eyelid
MONDO:0002139	sigmoid disease
MONDO:0002134	physiological sexual disorder
MONDO:0004797	mononeuritis of lower limb
MONDO:0004796	infectious meningitis
MONDO:0002135	optic nerve disease
MONDO:0004799	ulcerative blepharitis
MONDO:0002136	eczematous dermatitis of eyelid
MONDO:0002137	noninfectious dermatoses of eyelid
MONDO:0004798	Sheehan syndrome
MONDO:0004793	uterine corpus cancer
MONDO:0002130	upper limb mononeuronitis
MONDO:0004792	cancer of isthmus of fallopian tube
MONDO:0002131	jaw cancer
MONDO:0004795	otitis externa
MONDO:0002132	skull cancer
MONDO:0004794	exposure keratitis
MONDO:0002133	chronic rheumatic pericarditis
MONDO:0004791	lipid storage disease
MONDO:0004790	fatty liver disease
MONDO:0014127	oculocutaneous albinism type 5
MONDO:0014126	Perrault syndrome 4
MONDO:0014125	symphalangism, proximal, 1B
MONDO:0014124	Adams-Oliver syndrome 4
MONDO:0016786	partial hydatidiform mole
MONDO:0016787	epithelioid trophoblastic tumor
MONDO:0014129	autosomal recessive limb-girdle muscular dystrophy type 2R
MONDO:0016788	genetic hyperferritinemia without iron overload
MONDO:0016789	pyruvate metabolism disorder
MONDO:0014128	TCF12-related craniosynostosis
MONDO:0016782	paternal 14q32.2 hypomethylation syndrome
MONDO:0016783	maternal 14q32.2 hypermethylation syndrome
MONDO:0016784	gestational trophoblastic disease
MONDO:0016785	complete hydatidiform mole
MONDO:0014123	primary ciliary dyskinesia 21
MONDO:0014122	myofibromatosis, infantile, 2
MONDO:0014121	autosomal dominant childhood-onset proximal spinal muscular atrophy with contractures
MONDO:0016780	paternal 14q32.2 microdeletion syndrome
MONDO:0016781	maternal 14q32.2 microdeletion syndrome
MONDO:0014120	muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A13
MONDO:0002149	reproductive system cancer
MONDO:0002145	sex differentiation disease
MONDO:0002146	hypogonadism
MONDO:0002147	Coffin-Siris syndrome
MONDO:0002148	sphingolipidosis
MONDO:0002141	cutaneous undifferentiated pleomorphic sarcoma
MONDO:0002142	undifferentiated pleomorphic sarcoma
MONDO:0002143	vaginal yolk sac tumor
MONDO:0002144	hyperuricemia
MONDO:0002140	vagina sarcoma
MONDO:0014116	complex cortical dysplasia with other brain malformations 2
MONDO:0016779	multiple congenital anomalies due to 14q32.2 maternally expressed gene defect
MONDO:0014115	hypomyelination with brain stem and spinal cord involvement and leg spasticity
MONDO:0014114	cardiofaciocutaneous syndrome 4
MONDO:0014113	cardiofaciocutaneous syndrome 3
MONDO:0016775	lichen planus pemphigoides
MONDO:0016776	frontal fibrosing alopecia
MONDO:0014119	intellectual disability-strabismus syndrome
MONDO:0016777	inhalational botulism
MONDO:0014118	congenital neutropenia-myelofibrosis-nephromegaly syndrome
MONDO:0016778	iatrogenic botulism
MONDO:0014117	Charcot-Marie-Tooth disease type 4B3
MONDO:0016771	annular atrophic lichen planus
MONDO:0016772	annular lichen planus
MONDO:0016773	atrophic lichen planus
MONDO:0016774	lichen planus pigmentosus
MONDO:0014112	cardiofaciocutaneous syndrome 2
MONDO:0014111	cataract 19 multiple types
MONDO:0014110	cataract 15 multiple types
MONDO:0016770	actinic lichen planus
MONDO:0004779	epididymitis
MONDO:0002116	malignant exocrine pancreas neoplasm
MONDO:0002117	pancreas sarcoma
MONDO:0004778	epididymo-orchitis
MONDO:0002118	urinary system disease
MONDO:0002119	ossifying fibroma
MONDO:0028743	dysostosis with brachydactyly with extraskeletal manifestations
MONDO:0002112	benign peritoneal mesothelioma
MONDO:0004775	lens-induced iridocyclitis
MONDO:0002113	peritoneal carcinoma
MONDO:0004774	gonococcal iridocyclitis
MONDO:0004777	acute laryngitis
MONDO:0002114	pancreas lymphoma
MONDO:0004776	infectious anterior uveitis
MONDO:0002115	pancreatic cancer
MONDO:0004771	Fuchs' heterochromic uveitis
MONDO:0004770	exophthalmos
MONDO:0002110	adrenal rest tumor
MONDO:0004773	iridocyclitis
MONDO:0004772	glaucomatocyclitic crisis
MONDO:0002111	peritoneal mesothelioma
MONDO:0028742	dysostosis with brachydactyly without extraskeletal manifestations
MONDO:0028741	overgrowth or tall stature syndrome with skeletal involvement
MONDO:0014105	hypogonadotropic hypogonadism 19 with or without anosmia
MONDO:0016768	rare mucosal lichen planus
MONDO:0016769	linear lichen planus
MONDO:0014104	cerebellar ataxia, intellectual disability, and dysequilibrium syndrome 4
MONDO:0014103	hypogonadotropic hypogonadism 18 with or without anosmia
MONDO:0014102	hypogonadotropic hypogonadism 17 with or without anosmia
MONDO:0016764	isolated anophthalmia-microphthalmia syndrome
MONDO:0014109	NGLY1-deficiency
MONDO:0016765	19p13.12 microdeletion syndrome
MONDO:0014108	Fanconi anemia complementation group Q
MONDO:0016766	rare lichen planus
MONDO:0014107	hypogonadotropic hypogonadism 21 with or without anosmia
MONDO:0016767	cutaneous lichen planus
MONDO:0014106	hypogonadotropic hypogonadism 20 with or without anosmia
MONDO:0016760	microcephaly-microcornea syndrome, Seemanova type
MONDO:0016761	spondyloepiphyseal dysplasia
MONDO:0016762	microcornea-corectopia-macular hypoplasia syndrome
MONDO:0016763	spondylometaphyseal dysplasia
MONDO:0002109	pituitary cancer
MONDO:0014101	muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 12
MONDO:0014100	dilated cardiomyopathy 1KK
MONDO:0002127	urethral stricture
MONDO:0002128	mononeuritis multiplex
MONDO:0004789	cholangitis
MONDO:0002129	bone cancer
MONDO:0002123	calcinosis
MONDO:0004786	chronic cholangitis
MONDO:0002124	secondary lacrimal atrophy
MONDO:0004785	blepharitis
MONDO:0004788	cervix squamous papilloma
MONDO:0028737	biliary atresia disorder
MONDO:0002125	status epilepticus
MONDO:0004787	cervical mullerian papilloma
MONDO:0002126	childhood absence epilepsy
MONDO:0004782	diabetes insipidus
MONDO:0004781	acute myocardial infarction
MONDO:0002120	neuroendocrine carcinoma
MONDO:0002121	mononeuritis simplex
MONDO:0004784	allergic asthma
MONDO:0002122	neuritis
MONDO:0004783	panhypopituitarism
MONDO:0004780	strictly posterior acute myocardial infarction
MONDO:0016757	malignant triton tumor
MONDO:0016758	microcephaly-brain defect-spasticity-hypernatremia syndrome
MONDO:0016759	pontocerebellar hypoplasia type 2
MONDO:0200001	chromate resistance
MONDO:0200000	uterine ligament adenosarcoma
MONDO:0016753	benign schwannoma
MONDO:0016754	vestibular schwannoma
MONDO:0016755	neurofibroma
MONDO:0016756	inherited nervous system cancer-predisposing syndrome
MONDO:0016750	microcephaly-cleft palate syndrome
MONDO:0016751	malignant perineurioma
MONDO:0016752	benign peripheral nerve sheath tumor
MONDO:0004603	collagenopathy
MONDO:0004602	polymyalgia rheumatica
MONDO:0004605	chronic ulcer of skin
MONDO:0004604	Hodgkin's lymphoma, lymphocytic-histiocytic predominance
MONDO:0004601	ulcer of lower limbs
MONDO:0004600	monocytic leukemia
MONDO:0550003	SEC61B-related polycystic liver disease
MONDO:0002057	breast leiomyoma
MONDO:0002058	breast adenoma
MONDO:0002059	breast duct papilloma
MONDO:0002053	hypoglycemic coma
MONDO:0002054	breast cancer
MONDO:0002055	benign eccrine breast spiradenoma
MONDO:0002056	breast fibroadenoma
MONDO:0002050	depressive disorder
MONDO:0002051	integumentary system disease
MONDO:0002052	lymphadenitis
MONDO:0014049	urofacial syndrome 2
MONDO:0014048	Cowden syndrome 6
MONDO:0014047	Cowden syndrome 5
MONDO:0041656	ST-elevation myocardial infarction
MONDO:0014042	left ventricular noncompaction 7
MONDO:0014041	autism, susceptibility to, 19
MONDO:0014040	autosomal recessive osteopetrosis 8
MONDO:0014046	Cowden syndrome 4
MONDO:0014045	Cowden syndrome 3
MONDO:0014044	dysmorphism-conductive hearing loss-heart defect syndrome
MONDO:0014043	microcephalic primordial dwarfism due to ZNF335 deficiency
MONDO:0002068	female breast lower-inner quadrant cancer
MONDO:0002069	female breast axillary tail cancer
MONDO:0002064	breast angiomatosis
MONDO:0002065	benign breast adenomyoepithelioma
MONDO:0002066	breast adenomyoepithelioma
MONDO:0002067	female breast upper-inner quadrant cancer
MONDO:0002060	intraductal papilloma
MONDO:0002061	intraductal papillary breast neoplasm
MONDO:0002062	breast myofibroblastoma
MONDO:0002063	breast papillomatosis
MONDO:0014039	mitochondrial DNA depletion syndrome 11
MONDO:0014038	colorectal cancer, susceptibility to, 12
MONDO:0014037	spermatogenic failure 11
MONDO:0014036	Alzheimer disease 17
MONDO:0016698	ependymoma
MONDO:0016699	myxopapillary ependymoma
MONDO:0014031	microcephalic primordial dwarfism, Alazami type
MONDO:0016694	Pituicytoma
MONDO:0016695	oligodendroglioma
MONDO:0014030	primary ciliary dyskinesia 20
MONDO:0016696	anaplastic oligodendroglioma
MONDO:0016697	low grade ependymoma
MONDO:0016690	pleomorphic xanthoastrocytoma
MONDO:0014035	severe intellectual disability-progressive spastic diplegia syndrome
MONDO:0016691	pilocytic astrocytoma
MONDO:0014034	severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome
MONDO:0014033	dystonia 25
MONDO:0016692	pilomyxoid astrocytoma
MONDO:0014032	brachydactyly type A1C
MONDO:0016693	subependymal giant cell astrocytoma
MONDO:0002039	cognitive disorder
MONDO:0002035	colon lymphoma
MONDO:0004698	intestine carcinoma in situ
MONDO:0002036	penile disease
MONDO:0004697	esophageal leukoplakia
MONDO:0002037	pleural disease
MONDO:0004699	gastrointestinal lymphoma
MONDO:0002038	head and neck carcinoma
MONDO:0004694	hepatopulmonary syndrome
MONDO:0002031	cecal disease
MONDO:0002032	colon carcinoma
MONDO:0004693	squamous carcinoma in situ
MONDO:0004696	larynx carcinoma in situ
MONDO:0002033	cecum cancer
MONDO:0004695	liver lymphoma
MONDO:0002034	cecum lymphoma
MONDO:0004690	tonsillar fossa cancer
MONDO:0004692	choledochal cyst
MONDO:0004691	autosomal dominant polycystic kidney disease
MONDO:0002030	chronic cervicitis
MONDO:0014028	distal arthrogryposis type 5D
MONDO:0014027	hypotrichosis 11
MONDO:0014026	congenital stationary night blindness 1F
MONDO:0014025	lower motor neuron syndrome with late-adult onset
MONDO:0016687	protoplasmic astrocytoma
MONDO:0016688	fibrillary astrocytoma
MONDO:0016689	gemistocytic astrocytoma
MONDO:0014029	osteogenesis imperfecta type 14
MONDO:0014020	hereditary spastic paraplegia 55
MONDO:0016683	gliomatosis cerebri
MONDO:0016684	anaplastic astrocytoma
MONDO:0016685	low-grade astrocytoma
MONDO:0016686	diffuse astrocytoma
MONDO:0014024	hereditary spastic paraplegia 43
MONDO:0014023	congenital muscular dystrophy with intellectual disability and severe epilepsy
MONDO:0016680	high grade astrocytic tumor
MONDO:0016681	gliosarcoma
MONDO:0014022	muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 10
MONDO:0014021	familial episodic pain syndrome with predominantly upper body involvement
MONDO:0016682	giant cell glioblastoma
MONDO:0002046	alcohol abuse
MONDO:0002047	pulmonary systemic sclerosis
MONDO:0002048	thrombocytopenia due to immune destruction
MONDO:0002049	thrombocytopenia
MONDO:0002042	mechanical ectropion
MONDO:0002043	ectropion
MONDO:0002044	spastic ectropion
MONDO:0002045	communicating hydrocephalus
MONDO:0002040	dermatomycosis
MONDO:0002041	fungal infectious disease
MONDO:0014017	autism, susceptibility to, 18
MONDO:0014016	hereditary spastic paraplegia 49
MONDO:0014015	hereditary spastic paraplegia 56
MONDO:0014014	epidermolysis bullosa simplex due to exophilin 5 deficiency
MONDO:0016676	recurrent infections-inflammatory syndrome due to zinc metabolism disorder syndrome
MONDO:0016677	toxic or drug-related embryofetopathy
MONDO:0016678	maternal disease-related embryofetopathy
MONDO:0014019	dystonia 24
MONDO:0014018	hereditary spastic paraplegia 54
MONDO:0016679	rare tumor of neuroepithelial tissue
MONDO:0016672	hereditary persistence of fetal hemoglobin-sickle cell disease syndrome
MONDO:0016673	localized junctional epidermolysis bullosa, non-Herlitz type
MONDO:0016674	46,XY partial gonadal dysgenesis
MONDO:0016675	distal arthrogryposis type 10
MONDO:0014013	maternal riboflavin deficiency
MONDO:0014012	Charcot-Marie-Tooth disease axonal type 2Q
MONDO:0014011	autosomal recessive congenital ichthyosis 10
MONDO:0016670	sickle cell-hemoglobin d disease syndrome
MONDO:0014010	autosomal recessive congenital ichthyosis 9
MONDO:0016671	sickle cell-hemoglobin E disease syndrome
MONDO:0014082	cryptosporidiosis-chronic cholangitis-liver disease syndrome
MONDO:0014081	severe combined immunodeficiency due to CARD11 deficiency
MONDO:0014080	osteosclerotic metaphyseal dysplasia
MONDO:0002097	ocular melanoma
MONDO:0002098	facial nerve disease
MONDO:0002099	Histoplasma capsulatum infectious disease
MONDO:0100400	acute myeloid leukemia, t(3;12)(q23;p12.3)
MONDO:0002093	acanthoma
MONDO:0100401	acute myeloid leukemia, del(5q31-q32)
MONDO:0100402	acute myeloid leukemia, del(13q14-q21)
MONDO:0002094	conjunctival squamous cell carcinoma
MONDO:0002095	vascular cancer
MONDO:0100403	acute myeloid leukemia, loss of chromosome 17p
MONDO:0002096	malignant conjunctival melanoma
MONDO:0100404	acute myeloid leukemia, MLL gene rearrangement
MONDO:0002090	eccrine sweat gland neoplasm
MONDO:0002091	cryptosporidiosis
MONDO:0002092	small intestine leiomyoma
MONDO:0014086	osteogenesis imperfecta type 15
MONDO:0014085	hydrocephalus, nonsyndromic, autosomal recessive 2
MONDO:0014084	ataxia with oculomotor apraxia type 3
MONDO:0014083	agammaglobulinemia 7, autosomal recessive
MONDO:0014089	corneal intraepithelial dyskeratosis-palmoplantar hyperkeratosis-laryngeal dyskeratosis syndrome
MONDO:0014088	advanced sleep phase syndrome 2
MONDO:0014087	Smith-McCort dysplasia 2
MONDO:0014071	muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 11
MONDO:0014070	oculocutaneous albinism type 7
MONDO:0100410	acute myeloid leukemia, t(16;21)(p11;q22)
MONDO:0100411	acute myeloid leukemia, NPM1 gene mutation
MONDO:0100412	acute myeloid leukemia, monoallelic CEBPA gene mutation
MONDO:0100413	acute myeloid leukemia, biallelic CEBPA gene mutation
MONDO:0100414	acute myeloid leukemia, CEBPA gene mutation
MONDO:0100415	acute myeloid leukemia, FLT3 internal tandem duplication
MONDO:0100405	acute myeloid leukemia, Non-KMT2A MLLT10 rearrangement positive
MONDO:0100406	acute myeloid leukemia, inv(16)(p13.3;q24.3)
MONDO:0100407	acute myeloid leukemia, t(11;15)(p15;q35)
MONDO:0100408	acute myeloid leukemia, t(16;21)(q24;q22)
MONDO:0100409	acute myeloid leukemia, t(3;5)(q25;q34)
MONDO:0014075	cataract 39 multiple types
MONDO:0014074	Charcot-Marie-Tooth disease dominant intermediate F
MONDO:0014073	dilated cardiomyopathy 1II
MONDO:0014072	D,L-2-hydroxyglutaric aciduria
MONDO:0014079	restless legs syndrome, susceptibility to, 8
MONDO:0014078	platelet-type bleeding disorder 15
MONDO:0014077	cobblestone lissencephaly without muscular or ocular involvement
MONDO:0014076	dyskeratosis congenita, autosomal recessive 5
MONDO:0014060	progressive retinal dystrophy due to retinol transport defect
MONDO:0002079	neuroendocrine tumor
MONDO:0002075	spontaneous tension pneumothorax
MONDO:0100420	acute myeloid leukemia, KIT gene mutation
MONDO:0002076	pneumothorax
MONDO:0100421	acute myeloid leukemia, GATA1 gene mutation
MONDO:0002077	low implantation of placenta
MONDO:0100422	acute myeloid leukemia, RUNX1 gene mutation
MONDO:0002078	heart septal defect
MONDO:0100423	acute myeloid leukemia, PTPN11 gene mutation
MONDO:0002071	supratentorial cancer
MONDO:0002072	melanotic neuroectodermal tumor
MONDO:0100424	acute myeloid leukemia, NRAS gene mutation
MONDO:0002073	malignant pineal area germ cell neoplasm
MONDO:0100425	acute myeloid leukemia, KRAS gene mutation
MONDO:0002074	Behcet syndrome arthropathy
MONDO:0026045	prurigo nodularis
MONDO:0100416	acute myeloid leukemia, FLT3 tyrosine kinase domain point mutation
MONDO:0100417	acute myeloid leukemia, WT1 gene mutation
MONDO:0100418	acute myeloid leukemia, KIT exon 17 mutation
MONDO:0100419	acute myeloid leukemia, KIT exon 8 mutation
MONDO:0002070	ventricular septal defect
MONDO:0014069	syndactyly-camptodactyly and clinodactyly of fifth fingers-bifid toes syndrome
MONDO:0014064	mitochondrial complex III deficiency nuclear type 3
MONDO:0014063	mitochondrial complex III deficiency nuclear type 2
MONDO:0014062	mitochondrial DNA deletion syndrome with progressive myopathy
MONDO:0014061	Steel syndrome
MONDO:0014068	cone-rod dystrophy 17
MONDO:0014067	short ulna-dysmorphism-hypotonia-intellectual disability syndrome
MONDO:0014066	mitochondrial complex III deficiency nuclear type 5
MONDO:0014065	mitochondrial complex III deficiency nuclear type 4
MONDO:0002086	clear cell acanthoma
MONDO:0002087	peritoneum cancer
MONDO:0002088	partial retinal vein occlusion
MONDO:0002089	retinal vascular occlusion
MONDO:0002082	endocrine gland neoplasm
MONDO:0002083	Richter syndrome
MONDO:0002084	neuroectodermal tumor
MONDO:0002085	benign shuddering attacks
MONDO:0002080	congenital ichthyosiform erythroderma
MONDO:0014059	microphthalmia, isolated, with coloboma 9
MONDO:0100429	intrahepatic cholestasis of pregnancy
MONDO:0002081	musculoskeletal system disease
MONDO:0014058	facial dysmorphism-immunodeficiency-livedo-short stature syndrome
MONDO:0014053	stomatin-like protein-2, hyperphosphorylation of
MONDO:0014052	congenital myasthenic syndrome 8
MONDO:0014051	cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 2
MONDO:0014050	isolated microphthalmia 8
MONDO:0014057	maple syrup urine disease, mild variant
MONDO:0014056	melanoma, cutaneous malignant, susceptibility to, 9
MONDO:0014055	epilepsy, familial adult myoclonic, 4
MONDO:0014054	lymphoproliferative syndrome 2
MONDO:0004636	lip carcinoma in situ
MONDO:0004635	postcricoid region cancer
MONDO:0004638	lymphosarcoma
MONDO:0004637	aryepiglottic fold cancer
MONDO:0004632	Hodgkin's granuloma
MONDO:0004631	tongue cancer
MONDO:0004634	vein disease
MONDO:0004633	Hodgkin's lymphoma, mixed cellularity
MONDO:0004630	substance-induced psychosis
MONDO:0016618	rheumatoid factor-negative juvenile idiopathic arthritis without anti-nuclear antibodies
MONDO:0016619	autosomal recessive hypohidrotic ectodermal dysplasia
MONDO:0016625	acquired deficiency anemia
MONDO:0016626	hemolytic anemia due to glyceraldehyde-3-phosphate dehydrogenase deficiency
MONDO:0016627	rare hemorrhagic disorder
MONDO:0016628	hemorrhagic disorder due to a coagulation factors defect
MONDO:0016621	juvenile Huntington disease
MONDO:0016622	Melhem-Fahl syndrome
MONDO:0016623	rare deficiency anemia
MONDO:0016624	inherited deficiency anemia
MONDO:0016620	primary hypertrophic osteoarthropathy
MONDO:0004629	subacute delirium
MONDO:0004628	gastroduodenitis
MONDO:0004647	in situ carcinoma
MONDO:0004646	decubitus ulcer
MONDO:0004649	anaerobic pneumonia
MONDO:0004648	vascular dementia
MONDO:0004643	myeloid leukemia
MONDO:0004642	tonsillar pillar cancer
MONDO:0004645	cheek mucosa cancer
MONDO:0004644	subacute monocytic leukemia
MONDO:0004641	skin carcinoma in situ
MONDO:0004640	alcoholic gastritis
MONDO:0016607	odontohypophosphatasia
MONDO:0016608	megalencephaly
MONDO:0016609	inflammatory myopathy with abundant macrophages
MONDO:0016614	autosomal recessive ataxia due to PEX10 deficiency
MONDO:0016615	oligoarticular juvenile idiopathic arthritis with anti-nuclear antibodies
MONDO:0016616	oligoarticular juvenile idiopathic arthritis without anti-nuclear antibodies
MONDO:0016617	rheumatoid factor-negative juvenile idiopathic arthritis with anti-nuclear antibodies
MONDO:0016610	idiopathic eosinophilic myositis
MONDO:0016611	lipoblastoma
MONDO:0016612	X-linked cerebellar ataxia
MONDO:0016613	APC-related attenuated familial adenomatous polyposis
MONDO:0004639	perinatal necrotizing enterocolitis
MONDO:0004614	chronic monocytic leukemia
MONDO:0004613	acute intestinal ischemia
MONDO:0004616	herpetic whitlow
MONDO:0004615	upper gum cancer
MONDO:0004610	multiple carboxylase deficiency
MONDO:0004612	malignant histiocytosis
MONDO:0004611	soft palate cancer
MONDO:0016603	citrullinemia type II
MONDO:0016604	dysraphism-cleft lip/palate-limb reduction defects syndrome
MONDO:0016605	perinatal lethal hypophosphatasia
MONDO:0016606	prenatal benign hypophosphatasia
MONDO:0016600	acute neonatal citrullinemia type I
MONDO:0016601	adult-onset citrullinemia type I
MONDO:0016602	citrin deficiency
MONDO:0004607	vallecula cancer
MONDO:0004606	pyoderma gangrenosum
MONDO:0004609	herpes simplex infectious disease
MONDO:0004608	oropharynx cancer
MONDO:0004625	phlebitis
MONDO:0004624	uvula cancer
MONDO:0004627	duodenitis
MONDO:0004626	Hodgkin's paragranuloma
MONDO:0004621	upper lip cancer
MONDO:0004620	Hodgkin's lymphoma, lymphocytic depletion
MONDO:0004623	prostate carcinoma in situ
MONDO:0004622	chronic intestinal vascular insufficiency
MONDO:0004618	diplegia of upper limb
MONDO:0004617	recurrent hypersomnia
MONDO:0004619	measles
MONDO:0002017	olivopontocerebellar atrophy
MONDO:0004679	leukoplakia of vagina
MONDO:0002018	Leber congenital amaurosis
MONDO:0002019	hypohidrotic ectodermal dysplasia
MONDO:0002013	lymphangioma
MONDO:0004676	progressive myoclonus epilepsy
MONDO:0002014	autosomal recessive Ehlers-Danlos syndrome, vascular type
MONDO:0004675	mitochondrial encephalomyopathy
MONDO:0004678	dermatophytosis
MONDO:0002015	brittle cornea syndrome
MONDO:0002016	benign familial neonatal epilepsy
MONDO:0004677	tinea nigra
MONDO:0004672	fasciolopsiasis
MONDO:0002010	FG syndrome
MONDO:0004671	penis carcinoma in situ
MONDO:0004674	chorioretinitis
MONDO:0002011	hereditary angioedema
MONDO:0002012	methylmalonic acidemia
MONDO:0004673	lower lip cancer
MONDO:0004670	lupus erythematosus
MONDO:0016669	sickle cell-hemoglobin c disease syndrome
MONDO:0014006	Schuurs-Hoeijmakers syndrome
MONDO:0014005	immunoglobulin-mediated membranoproliferative glomerulonephritis
MONDO:0014004	basal ganglia calcification, idiopathic, 4
MONDO:0014003	developmental and epileptic encephalopathy, 15
MONDO:0016665	unclassified vasculitis
MONDO:0016666	unexplained long-lasting fever/inflammatory syndrome
MONDO:0014009	autosomal recessive congenital ichthyosis 7
MONDO:0016667	sickle cell disease associated with an other hemoglobin anomaly
MONDO:0014008	phosphohydroxylysinuria
MONDO:0016668	sickle cell-beta-thalassemia disease syndrome
MONDO:0014007	Aicardi-Goutieres syndrome 6
MONDO:0016661	infantile onset panniculitis with uveitis and systemic granulomatosis
MONDO:0016662	idiopathic recurrent pericarditis
MONDO:0016663	overlapping connective tissue disease
MONDO:0016664	drug-induced vasculitis
MONDO:0014002	autosomal dominant nocturnal frontal lobe epilepsy 5
MONDO:0014001	Usher syndrome type 1K
MONDO:0014000	congenital heart defects, multiple types, 2
MONDO:0016660	autosomal recessive primary microcephaly
MONDO:0002028	personality disorder
MONDO:0002029	chronic gonorrhea of cervix
MONDO:0004687	severe nonproliferative diabetic retinopathy
MONDO:0002024	cholera
MONDO:0002025	psychiatric disorder
MONDO:0004686	lattice corneal dystrophy
MONDO:0002026	candidiasis
MONDO:0004689	inborn metal metabolism disorder
MONDO:0002027	avoidant personality disorder
MONDO:0004688	sideroblastic anemia
MONDO:0004683	Evans' syndrome
MONDO:0002020	Blount disease
MONDO:0004682	retromolar area cancer
MONDO:0002021	gingival disease
MONDO:0002022	disease of orbital region
MONDO:0004685	Waldeyer's ring cancer
MONDO:0002023	cystic echinococcosis
MONDO:0004684	plantar fibromatosis
MONDO:0004681	learning disability
MONDO:0004680	primary thrombocytopenia
MONDO:0016658	8p23.1 microdeletion syndrome
MONDO:0016659	8p23.1 duplication syndrome
MONDO:0016654	ring chromosome 5
MONDO:0016655	6p22 microdeletion syndrome
MONDO:0016656	7q31 microdeletion syndrome
MONDO:0016657	8p11.2 deletion syndrome
MONDO:0016650	paternal uniparental disomy of chromosome 1
MONDO:0016651	maternal uniparental disomy of chromosome 1
MONDO:0016652	2q31.1 microdeletion syndrome
MONDO:0016653	2q33.1 microdeletion syndrome
MONDO:0004658	breast carcinoma in situ
MONDO:0004657	disseminated chorioretinitis
MONDO:0004659	eye carcinoma in situ
MONDO:0004654	pyomyositis
MONDO:0004653	atypical chronic myeloid leukemia, BCR-ABL1 negative
MONDO:0004656	rubella
MONDO:0004655	acute megakaryoblastic leukemia
MONDO:0004650	malignant carotid body paraganglioma
MONDO:0004652	bacterial pneumonia
MONDO:0004651	smallpox
MONDO:0016647	autosomal recessive Stickler syndrome
MONDO:0016648	multiple epiphyseal dysplasia
MONDO:0016649	Warburg micro syndrome
MONDO:0016643	frontonasal dysplasia
MONDO:0016644	logopenic progressive aphasia
MONDO:0016645	rare neoplastic disease
MONDO:0016646	autosomal dominant optic atrophy and peripheral neuropathy
MONDO:0016640	fibrous dysplasia of bone
MONDO:0016641	limb transversal defect-cardiac anomaly syndrome
MONDO:0016642	meningioma
MONDO:0004669	salivary gland cancer
MONDO:0002006	serous labyrinthitis
MONDO:0004668	fascioliasis
MONDO:0002007	VACTERL association
MONDO:0002008	labyrinthitis
MONDO:0002009	major depressive disorder
MONDO:0004665	nodular sclerosis classical Hodgkin lymphoma
MONDO:0002002	postsurgical hypothyroidism
MONDO:0028618	gastroenteric neuroendocrine neoplasm
MONDO:0004664	helminthiasis
MONDO:0002003	papilledema
MONDO:0004667	sublingual gland cancer
MONDO:0002004	atheroembolism of kidney
MONDO:0002005	acrodysostosis
MONDO:0004666	metagonimiasis
MONDO:0004661	trachea carcinoma in situ
MONDO:0004660	lung carcinoma in situ
MONDO:0004663	colon carcinoma in situ
MONDO:0002000	anaerobic meningitis
MONDO:0004662	heterophyiasis
MONDO:0002001	disease of cellular proliferation
MONDO:0016629	hemorrhagic disorder due to a platelet anomaly
MONDO:0016636	thrombotic disorder due to a constitutional platelet anomaly
MONDO:0016637	thrombotic disorder due to an acquired platelet anomaly
MONDO:0016638	familial hypodysfibrinogenemia
MONDO:0016639	lower limb deficiency-hypospadias syndrome
MONDO:0016632	thrombotic disorder due to a coagulation factors defect
MONDO:0016633	thrombotic disorder due to a constitutional coagulation factors defect
MONDO:0016634	thrombotic disorder due to an acquired coagulation factors defect
MONDO:0016635	thrombotic disorder due to a platelet anomaly
MONDO:0016630	isolated delta-storage pool disease
MONDO:0016631	hemorrhagic disorder due to an acquired platelet anomaly
MONDO:0100320	post-COVID-19 disorder
MONDO:0100321	viral disease or post-viral disorder
MONDO:0100322	non-Zellweger spectrum disorder
MONDO:0100325	odontochondrodysplasia 1
MONDO:0100326	Glanzmann thrombasthenia
MONDO:0100327	hypercholanemia, familial
MONDO:0100318	SARS-CoV-2-related disease
MONDO:0100319	COVID-19–associated multisystem inflammatory syndrome in adults
MONDO:0100330	disease arising from reactivation of latent virus
MONDO:0100332	disease has primary infectious agent
MONDO:0100333	disease caused by reactivation of latent infectious agent
MONDO:0100334	viral infectious disease or sequela
MONDO:0100336	infectious disease or post-infectious disorder
MONDO:0100337	SEC61A1 deficiency
MONDO:0100338	urinary tract infection
MONDO:0100328	microcephaly, epilepsy, and diabetes syndrome
MONDO:0100329	primary viral infectious disease
MONDO:0100340	Friedreich ataxia 1
MONDO:0100342	malignant glioma
MONDO:0100343	antenatal Bartter syndrome
MONDO:0100344	Bartter disease type 1
MONDO:0100345	lactose intolerance
MONDO:0100347	carcinoid syndrome
MONDO:0100348	neurodevelopmental disorder with microcephaly, impaired language, and gait abnormalities
MONDO:0100349	COACH syndrome
MONDO:0100339	Friedreich ataxia
MONDO:0100350	neuronopathy, distal hereditary motor, type 5
MONDO:0100352	episodic kinesigenic dyskinesia 1
MONDO:0100353	HHV-7 infectious disease
MONDO:0100354	megacystis-microcolon-intestinal hypoperistalsis syndrome 1
MONDO:0100355	classic or non-classic genetic disease presentation
MONDO:0100356	classic presentation
MONDO:0100357	non-classic presentation
MONDO:0100358	ectodermal dysplasia WNT10A related
MONDO:0100359	herpes simplex type 1 infectious disease
MONDO:0100360	herpes simplex type 2 infectious disease
MONDO:0100361	lip herpes simplex type 1 infectious disease
MONDO:0100362	lip herpes simplex type 2 infectious disease
MONDO:0100363	genital herpes simplex type 2 infectious disease
MONDO:0100364	genital herpes simplex type 1 infectious disease
MONDO:0100365	mucopolysaccharidosis or mucopolysaccharidosis-like disorder
MONDO:0100366	occupational disorder
MONDO:0100367	port-wine nevi-mega cisterna magna-hydrocephalus syndrome
MONDO:0100370	acute hepatitis B virus infection
MONDO:0100371	acute hepatitis C virus infection
MONDO:0100372	disorder of peroxisomal transporter
MONDO:0100373	acute myeloid leukemia, inv(16)(p13.1;q22)
MONDO:0100374	acute myeloid leukemia, t(16;16)(p13.1;q22)
MONDO:0100375	acute myeloid leukemia, t(15;17)(q24;q21)
MONDO:0100376	acute myeloid leukemia, t(9;11)(p21.3;q23.3)
MONDO:0100377	acute myeloid leukemia, t(10;11)(p12;q23)
MONDO:0100378	acute myeloid leukemia, t(10;11)(p11.2;q23)
MONDO:0100379	acute myeloid leukemia, t(1;11)(q21;q23)
MONDO:0100380	acute myeloid leukemia, t(4;11)(q21;q23)
MONDO:0100381	acute myeloid leukemia, t(6;11)(q27;q23)
MONDO:0100382	acute myeloid leukemia, t(6;9)(p23;q34.1)
MONDO:0100383	acute myeloid leukemia, t(11;19)(q23;p13)
MONDO:0100384	acute myeloid leukemia, t(11;19)(q23;p13.1)
MONDO:0100385	acute myeloid leukemia, t(11;19)(q23.3;p13.3)
MONDO:0100386	acute myeloid leukemia, t(v;11q23.3)
MONDO:0100387	acute myeloid leukemia, Monosomy 7
MONDO:0100388	acute myeloid leukemia, Monosomy 5
MONDO:0100389	acute myeloid leukemia, Trisomy 8
MONDO:0100390	acute myeloid leukemia, der12p
MONDO:0100391	acute myeloid leukemia, t(2;12)
MONDO:0100392	acute myeloid leukemia, t(11;17)
MONDO:0100393	acute myeloid leukemia, t(8;16)
MONDO:0100394	acute myeloid leukemia, t(1;22)
MONDO:0100395	acute myeloid leukemia, t(5;11)(q35;p15)
MONDO:0100396	acute myeloid leukemia, t(7;12)(q36;p13)
MONDO:0100397	acute myeloid leukemia, t(9;22)(q34.1;q11.2)
MONDO:0100398	acute myeloid leukemia, inv(3)(q21.3;q26.2)
MONDO:0100399	acute myeloid leukemia, t(3;3)(q21.3;q26.2)
MONDO:0004599	barbiturate abuse
MONDO:0004598	acute cor pulmonale
MONDO:0004595	acute pulmonary heart disease
MONDO:0004594	puerperal pulmonary embolism
MONDO:0004597	pulmonary embolism and infarction
MONDO:0004596	cor pulmonale
MONDO:0004591	impetigo herpetiformis
MONDO:0004590	fundus dystrophy
MONDO:0004593	Bartholin duct cyst
MONDO:0004592	impetigo
MONDO:0016588	infantile mercury poisoning
MONDO:0016589	progressive cerebello-cerebral atrophy
MONDO:0041535	mesenteric lymphadenitis due to Yersinia infection
MONDO:0041536	Far-East scarlet-like fever
MONDO:0016584	mandibuloacral dysplasia
MONDO:0016585	mansonelliasis
MONDO:0016586	systemic mastocytosis
MONDO:0016587	arrhythmogenic right ventricular cardiomyopathy
MONDO:0016580	congenital pulmonary airway malformation
MONDO:0016581	conotruncal heart malformations
MONDO:0016582	congenital mitral malformation
MONDO:0016583	familial intestinal malrotation-facial anomalies syndrome
MONDO:0016577	biliary atresia with splenic malformation syndrome
MONDO:0016578	mitochondrial oxidative phosphorylation disorder due to nuclear DNA anomalies
MONDO:0016579	dominant hypophosphatemia with nephrolithiasis or osteoporosis
MONDO:0016573	acute fatty liver of pregnancy
MONDO:0016574	hypo- and hypermelanotic cutaneous macules-retarded growth-intellectual disability syndrome
MONDO:0016575	primary ciliary dyskinesia
MONDO:0016576	split hand-foot malformation
MONDO:0016570	primary pulmonary lymphoma
MONDO:0016571	macrocephaly-short stature-paraplegia syndrome
MONDO:0016572	central bilateral macrogyria
MONDO:0004577	corneal ulcer
MONDO:0004576	pellagra
MONDO:0004579	retinoschisis
MONDO:0004578	flat retinoschisis
MONDO:0004573	ariboflavinosis
MONDO:0004572	cyclothymic disorder
MONDO:0004575	choline deficiency disease
MONDO:0004574	pyridoxine deficiency anemia
MONDO:0004571	intestinal impaction
MONDO:0004570	intestinal volvulus
MONDO:0016566	loiasis
MONDO:0016567	locked-in syndrome
MONDO:0016568	Lowe-Kohn-Cohen syndrome
MONDO:0016569	rare lymphatic malformation
MONDO:0016562	progressive supranuclear palsy-pure akinesia with gait freezing syndrome
MONDO:0016563	progressive supranuclear palsy-corticobasal syndrome
MONDO:0016564	progressive supranuclear palsy-progressive non-fluent aphasia syndrome
MONDO:0016565	syndromic genetic obesity
MONDO:0016560	ptosis-syndactyly-learning difficulties syndrome
MONDO:0016561	1q44 microdeletion syndrome
MONDO:0004588	night blindness
MONDO:0004587	hereditary night blindness
MONDO:0004589	hereditary retinal dystrophy
MONDO:0004584	maple bark strippers' lung
MONDO:0004583	transient retinal arterial occlusion
MONDO:0004586	rheumatoid lung disease
MONDO:0004585	polyhydramnios
MONDO:0004580	retinal degeneration
MONDO:0004582	rheumatic myocarditis
MONDO:0004581	localized scleroderma
MONDO:0016559	glaucoma secondary to spherophakia/ectopia lentis and megalocornea
MONDO:0016555	transient congenital hypothyroidism due to maternal factor
MONDO:0016556	transient congenital hypothyroidism due to neonatal factor
MONDO:0016557	leukonychia totalis
MONDO:0016558	familial congenital mirror movements
MONDO:0016551	congenital primary megaureter, refluxing form
MONDO:0016552	congenital primary megaureter, nonrefluxing and unobstructed form
MONDO:0016553	isolated congenital hypogonadotropic hypogonadism
MONDO:0016554	neonatal iodine exposure
MONDO:0016550	congenital primary megaureter, obstructed form
MONDO:0100304	disorder of bile acid aminotransferase
MONDO:0100305	bile acid CoA:amino acid N-acyltransferase deficiency
MONDO:0016590	collecting duct carcinoma
MONDO:0100310	hereditary cerebellar ataxia
MONDO:0100311	sensory ataxia
MONDO:0100312	vestibular ataxia
MONDO:0100315	isolated adrenal insufficiency
MONDO:0100316	long QT syndrome 1
MONDO:0100306	disorder of defective peroxisome oxidative status
MONDO:0041526	pregnancy disorder with abortive outcome
MONDO:0100307	adult Refsum disease due to PEX7 defect
MONDO:0100308	atactic disorder
MONDO:0100309	hereditary ataxia
MONDO:0016599	autosomal dominant secondary polycythemia
MONDO:0016595	inhalational anthrax
MONDO:0016596	hyperphosphatasia-intellectual disability syndrome
MONDO:0016597	generalized pustular psoriasis
MONDO:0016598	autosomal recessive secondary polycythemia not associated with VHL gene
MONDO:0016591	sporadic adult-onset ataxia of unknown etiology
MONDO:0016592	non-hereditary degenerative ataxia
MONDO:0016593	acquired ataxia
MONDO:0016594	superficial siderosis
MONDO:0004515	olfactory neural tumor
MONDO:0004514	chronic rhinitis
MONDO:0004517	ureter tuberculosis
MONDO:0004516	bulbomembranous urethral cancer
MONDO:0004511	lower clivus meningioma
MONDO:0004510	inflammatory liposarcoma
MONDO:0004513	adult pleomorphic rhabdomyosarcoma
MONDO:0004512	meningeal melanomatosis
MONDO:0016504	primary unilateral adrenal hyperplasia
MONDO:0016505	aldosterone-producing adrenal cortex adenoma
MONDO:0016506	ectopic aldosterone-producing tumor
MONDO:0016507	rare surgically correctable form of primary aldosteronism
MONDO:0016500	acute sensory ataxic neuropathy
MONDO:0016501	Hermansky-Pudlak syndrome with pulmonary fibrosis
MONDO:0016502	Hermansky-Pudlak syndrome without pulmonary fibrosis
MONDO:0016503	congenital erosive and vesicular dermatosis
MONDO:0004508	periapical periodontitis
MONDO:0004507	atypical breast papilloma
MONDO:0004509	intrahepatic biliary papillomatosis
MONDO:0004526	mixed endometrial stromal and smooth muscle tumor
MONDO:0004525	scabies
MONDO:0004528	lymph node palisaded myofibroblastoma
MONDO:0004527	congenital granular cell tumor
MONDO:0004522	peritonitis
MONDO:0004521	adult epithelioid sarcoma
MONDO:0004524	thyroid gland atypical follicular adenoma
MONDO:0004523	clear cell squamous cell skin carcinoma
MONDO:0004520	intratubular embryonal carcinoma
MONDO:0004519	synovial angioma
MONDO:0004518	anterior urethra cancer
MONDO:0004504	penile urethral cancer
MONDO:0004503	upper clivus meningioma
MONDO:0004506	microscopic breast papilloma
MONDO:0004505	central breast papilloma
MONDO:0004500	lung superior sulcus carcinoma
MONDO:0004502	parapharyngeal meningioma
MONDO:0004501	fallopian tube cystadenofibroma
MONDO:0004559	malignant glandular tumor of peripheral nerve sheath
MONDO:0004558	thyroid gland macrofollicular adenoma
MONDO:0004555	kidney angiomyolipoma
MONDO:0004554	childhood kidney angiomyolipoma
MONDO:0004557	congenital fibrosarcoma
MONDO:0004556	carcinoma arising in nasal papillomatosis
MONDO:0004551	Meckel diverticulitis
MONDO:0004550	malignant cornea melanoma
MONDO:0004553	extrinsic allergic alveolitis
MONDO:0004552	microinvasive cervical squamous cell carcinoma
MONDO:0016548	megacystis-megaureter syndrome
MONDO:0016549	primary megaureter, adult-onset form
MONDO:0016544	IgG4-related mesenteritis
MONDO:0016545	leukoencephalopathy-palmoplantar keratoderma syndrome
MONDO:0016546	primary orthostatic tremor
MONDO:0016547	Beckwith-Wiedemann syndrome due to NSD1 mutation
MONDO:0016540	congenital secondary polycythemia
MONDO:0016541	acquired secondary polycythemia
MONDO:0016542	immune dysregulation-inflammatory bowel disease-arthritis-recurrent infections syndrome
MONDO:0016543	hyperphenylalaninemia due to tetrahydrobiopterin deficiency
MONDO:0004569	brachial plexus neuropathy from injury
MONDO:0004566	postgastrectomy syndrome
MONDO:0004565	intestinal obstruction
MONDO:0004568	paralytic ileus
MONDO:0004567	ileus
MONDO:0004562	breast apocrine carcinoma in situ
MONDO:0004561	retinal melanoma
MONDO:0004564	thyroid malformation
MONDO:0004563	physiological polycythemia
MONDO:0004560	follicular infundibulum tumor
MONDO:0016537	lymphoproliferative syndrome
MONDO:0016538	hypotonia-cystinuria syndrome type 1
MONDO:0016539	atypical hypotonia-cystinuria syndrome
MONDO:0016533	apolipoprotein A-II amyloidosis
MONDO:0016534	infundibulo-neurohypophysitis
MONDO:0016535	hypohidrotic ectodermal dysplasia
MONDO:0016536	autosomal recessive lymphoproliferative disease
MONDO:0016530	laryngocele
MONDO:0016531	digestive duplication
MONDO:0016532	Lennox-Gastaut syndrome
MONDO:0004537	intestinal variant cervical mucinous adenocarcinoma
MONDO:0004536	villoglandular variant cervical mucinous adenocarcinoma
MONDO:0004539	aortic malignant tumor
MONDO:0004538	endocervical type cervical mucinous adenocarcinoma
MONDO:0004533	perineural angioma
MONDO:0004532	auditory system cancer
MONDO:0004535	childhood choriocarcinoma of the ovary
MONDO:0004534	microglandular adenosis of breast
MONDO:0004531	sclerosing adenosis of breast
MONDO:0004530	early invasive cervical adenocarcinoma
MONDO:0016519	keratosis follicularis spinulosa decalvans
MONDO:0016526	trisomy 9p
MONDO:0016527	glycogen storage disease due to lactate dehydrogenase deficiency
MONDO:0016528	limb body wall complex
MONDO:0016529	duplication of urethra
MONDO:0016522	Kousseff syndrome
MONDO:0016523	bronchogenic cyst
MONDO:0016524	congenital vascular bone syndrome
MONDO:0016525	familial hyperaldosteronism
MONDO:0016520	isolated Klippel-Feil syndrome
MONDO:0016521	muscular pseudohypertrophy-hypothyroidism syndrome
MONDO:0004529	non-ossifying fibromyxoid tumor
MONDO:0004548	adult type testicular granulosa cell tumor
MONDO:0004547	reticular pattern testicular yolk sac tumor
MONDO:0004549	cork-handlers' disease
MONDO:0004544	chordoid meningioma
MONDO:0004543	enteric pattern testicular yolk sac tumor
MONDO:0004546	lumbar plexus neoplasm
MONDO:0004545	adult malignant schwannoma
MONDO:0004540	epithelioid malignant peripheral nerve sheath tumor
MONDO:0004542	cervical adenosquamous carcinoma, glassy cell variant
MONDO:0004541	pseudoglandular variant testicular seminoma
MONDO:0016508	rare non surgically correctable form of primary aldosteronism
MONDO:0016509	microcornea-posterior megalolenticonus-persistent fetal vasculature-coloboma syndrome
MONDO:0016515	Kallmann syndrome-heart disease syndrome
MONDO:0016516	Kenny-Caffey syndrome
MONDO:0016517	rare genetic vascular disease
MONDO:0016518	isolated punctate palmoplantar keratoderma
MONDO:0016511	infectious embryofetopathy
MONDO:0016512	Kabuki syndrome
MONDO:0016513	alpha-thalassemia-related diseases
MONDO:0016514	epidermolysis bullosa simplex with anodontia/hypodontia
MONDO:0016510	epibulbar lipodermoid-preauricular appendage-polythelia syndrome
MONDO:0100280	Waldenstrom macroglobulinemia
MONDO:0100281	macroglobulinemia, Waldenstrom, 1
MONDO:0100282	SC phocomelia syndrome
MONDO:0100283	overgrowth syndrome and/or cerebral malformations due to abnormalities in MTOR pathway genes
MONDO:0100284	X-linked intellectual disability
MONDO:0100285	extrahepatic biliary atresia
MONDO:0100286	respiratory syncytial virus bronchiolitis
MONDO:0100288	enhanced S-cone syndrome
MONDO:0100289	Goldmann-Favre syndrome
MONDO:0100290	colon serrated polyposis
MONDO:0100291	early T cell progenitor acute lymphoblastic leukemia
MONDO:0100294	mitochondrial complex II deficiency, nuclear type 1
MONDO:0100296	Olmsted syndrome 1
MONDO:0100297	short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies 1
MONDO:0100203	parainfluenza virus type 1 infectious disease
MONDO:0100204	parainfluenza virus type 2 infectious disease
MONDO:0100205	parainfluenza virus type 4 infectious disease
MONDO:0100210	growth hormone insensitivity syndrome with immune dysregulation
MONDO:0100211	growth hormone insensitivity with immune dysregulation 1, autosomal recessive
MONDO:0100212	IFAP syndrome
MONDO:0100213	IFAP syndrome with or without BRESHECK syndrome
MONDO:0100214	Rajab interstitial lung disease with brain calcifications
MONDO:0100215	Rajab interstitial lung disease with brain calcifications 1
MONDO:0100209	X inactivation, familial skewed
MONDO:0100220	Rajab interstitial lung disease with brain calcifications 2
MONDO:0100221	IFAP syndrome 2
MONDO:0100222	A20 haploinsufficiency
MONDO:0100223	mitochondrial complex I deficiency, nuclear type
MONDO:0100224	mitochondrial complex I deficiency, nuclear type 1
MONDO:0100225	collagen 6-related myopathy
MONDO:0100226	parasomnia, sleepwalking type
MONDO:0100228	LAMA2-related muscular dystrophy
MONDO:0100218	arthrogryposis multiplex congenita 5
MONDO:0100219	growth hormone insensitivity syndrome with immune dysregulation 2, autosomal dominant
MONDO:0016390	familial hypoparathyroidism
MONDO:0016391	neonatal diabetes mellitus
MONDO:0016392	cerebellar hypoplasia-tapetoretinal degeneration syndrome
MONDO:0100230	fatty acyl-CoA reductase 1 dysregulation
MONDO:0100231	psoriatic arthritis, susceptibility to, 1
MONDO:0100232	psoriatic arthritis, susceptibility to
MONDO:0100233	long COVID-19
MONDO:0100234	paroxysmal familial ventricular fibrillation
MONDO:0100237	inherited cutis laxa
MONDO:0100238	inherited Fanconi renotubular syndrome
MONDO:0100239	inherited hypertrophic pyloric stenosis
MONDO:0100229	Heimler syndrome
MONDO:0016397	lysosomal disease with epilepsy
MONDO:0016398	peroxisomal disease with epilepsy
MONDO:0016399	amino acid or protein metabolism disease with epilepsy
MONDO:0016393	hyposmia-nasal and ocular hypoplasia-hypogonadotropic hypogonadism syndrome
MONDO:0016394	sporadic infantile bilateral striatal necrosis
MONDO:0016395	foveal hypoplasia-presenile cataract syndrome
MONDO:0016396	pontocerebellar hypoplasia type 1
MONDO:0100240	inherited thrombophilia
MONDO:0100241	inherited thrombocytopenia
MONDO:0100242	glioma susceptibility
MONDO:0100243	inherited paroxysmal nocturnal hemoglobinuria
MONDO:0100244	paroxysmal nocturnal hemoglobinuria
MONDO:0100245	acquired paroxysmal nocturnal hemoglobinuria
MONDO:0100246	migraine with or without aura, susceptibility to
MONDO:0100247	multiple congenital anomalies-hypotonia-seizures syndrome
MONDO:0100248	rapidly progressive primary central nervous system vasculitis
MONDO:0100249	46,XX testicular disorder of sex development
MONDO:0100250	46,XX sex reversal 1
MONDO:0100251	familial hyperphosphatemic tumoral calcinosis/hyperphosphatemic hyperostosis syndrome
MONDO:0100252	tumoral calcinosis, hyperphosphatemic, familial, 1
MONDO:0100253	Roberts-SC phocomelia syndrome
MONDO:0100255	adenosine kinase deficiency
MONDO:0100257	peroxisomal single enzyme/protein defect
MONDO:0100258	phytanoyl-CoA hydroxylase deficiency
MONDO:0100259	peroxisome biogenesis disorder due to PEX1 defect
MONDO:0100260	peroxisome biogenesis disorder due to PEX2 defect
MONDO:0100261	peroxisome biogenesis disorder due to PEX3 defect
MONDO:0100262	peroxisome biogenesis disorder due to PEX5 defect
MONDO:0100263	peroxisome biogenesis disorder due to PEX6 defect
MONDO:0100264	peroxisome biogenesis disorder due to PEX10 defect
MONDO:0100265	peroxisome biogenesis disorder due to PEX5 defect in the PEX7-binding domain
MONDO:0100266	peroxisome biogenesis disorder due to PEX12 defect
MONDO:0100267	peroxisome biogenesis disorder due to PEX13 defect
MONDO:0041366	acute epiglottitis
MONDO:0100268	peroxisome biogenesis disorder due to PEX14 defect
MONDO:0100269	peroxisome biogenesis disorder due to PEX16 defect
MONDO:0100270	peroxisome biogenesis disorder due to PEX19 defect
MONDO:0100271	peroxisome biogenesis disorder due to PEX26 defect
MONDO:0100272	peroxisome biogenesis disorder due to PEX7 defect
MONDO:0100273	glyceronephosphate O-acyltransferase deficiency
MONDO:0100274	alkylglycerone-phosphate synthase deficiency
MONDO:0100275	fatty acyl-CoA reductase defects
MONDO:0100276	disorder of defective peroxisomal and mitochondrial fission
MONDO:0100277	disorder of peroxisomal alpha oxidation
MONDO:0100278	alanine glyoxylate aminotransferase deficiency
MONDO:0100279	peroxisome biogenesis disorder due to PEX11B defect
MONDO:0004478	pregerminal center chronic lymphocytic leukemia/small lymphocytic lymphoma
MONDO:0004477	adrenal gland ganglioneuroblastoma
MONDO:0004479	malignant childhood germ cell neoplasm
MONDO:0004474	gallbladder lymphoma
MONDO:0004473	epiglottis cancer
MONDO:0004476	thymus sarcomatoid carcinoma
MONDO:0004475	thymus clear cell carcinoma
MONDO:0004470	osteochondrosis
MONDO:0004472	breast columnar cell mucinous carcinoma
MONDO:0004471	bacterial arthritis
MONDO:0016467	isotretinoin syndrome
MONDO:0016468	toxin-mediated infectious botulism
MONDO:0016469	Ehlers-Danlos syndrome, vascular-like type
MONDO:0016463	syndromic agammaglobulinemia
MONDO:0016464	insulin-resistance syndrome type B
MONDO:0016465	multiple intestinal atresia
MONDO:0016466	asbestosis
MONDO:0016460	polyvalvular heart disease syndrome
MONDO:0016461	5q35 microduplication syndrome
MONDO:0016462	isolated agammaglobulinemia
MONDO:0004489	fallopian tube gestational choriocarcinoma
MONDO:0004488	cervical atypical polypoid adenomyoma
MONDO:0004485	interstitial myocarditis
MONDO:0004484	gallbladder melanoma
MONDO:0004487	endometrial type cervical adenomyoma
MONDO:0004486	endocervical type cervical adenomyoma
MONDO:0004481	pancreatic intraductal papillary-mucinous neoplasm with an associated invasive carcinoma
MONDO:0004480	pancreatic invasive intraductal papillary-mucinous carcinoma
MONDO:0004483	thyroid gland oncocytic adenoma
MONDO:0004482	fibroosseous pseudotumor of the digits
MONDO:0016456	5q14.3 microdeletion syndrome
MONDO:0016457	ptosis-upper ocular movement limitation-absence of lacrimal punctum syndrome
MONDO:0016458	8q12 microduplication syndrome
MONDO:0016459	2q23.1 microdeletion syndrome
MONDO:0016452	idiopathic hypersomnia without long sleep time
MONDO:0016453	foodborne botulism
MONDO:0016454	severe early-onset axonal neuropathy due to NEFL deficiency
MONDO:0016455	virus-associated trichodysplasia spinulosa
MONDO:0016450	autoimmune hemolytic anemia, cold type
MONDO:0016451	idiopathic hypersomnia with long sleep time
MONDO:0004459	bladder hepatoid adenocarcinoma
MONDO:0004456	cocaine abuse
MONDO:0004455	classic congenital mesoblastic nephroma
MONDO:0004458	bladder mixed adenocarcinoma
MONDO:0004457	maxillary sinus Schneiderian papilloma
MONDO:0004452	childhood central nervous system germinoma
MONDO:0004451	sarcomatous intrahepatic cholangiocarcinoma
MONDO:0004454	cellular congenital mesoblastic nephroma
MONDO:0004453	testicular yolk sac tumor, myxomatous pattern
MONDO:0004450	carotid artery occlusion
MONDO:0041440	functional visual loss
MONDO:0016449	mid-dermal elastolysis
MONDO:0016445	familial anetoderma
MONDO:0016446	acquired cutis laxa
MONDO:0016447	white fibrous papulosis of the neck
MONDO:0016448	pseudoxanthoma elasticum-like papillary dermal elastolysis
MONDO:0016441	acquired pseudoxanthoma elasticum
MONDO:0016442	elastoma
MONDO:0016443	papular elastorrhexis
MONDO:0016444	primary anetoderma
MONDO:0016440	elastofibroma dorsi
MONDO:0004467	mature gastric teratoma
MONDO:0004466	neuronitis
MONDO:0004469	pseudovascular skin squamous cell carcinoma
MONDO:0004468	anal canal Paget disease
MONDO:0004463	cellular phase chronic idiopathic myelofibrosis
MONDO:0004462	extrahepatic bile duct cystadenoma
MONDO:0004465	periampullary adenocarcinoma
MONDO:0004464	nephrogenic adenoma of the urethra
MONDO:0004461	vaginal tubulovillous adenoma
MONDO:0004460	thyroid gland fetal adenoma
MONDO:0016438	linear focal dermal elastosis
MONDO:0016439	elastoderma
MONDO:0016434	acquired dermis elastic tissue disorder
MONDO:0016435	acquired dermis elastic tissue disorder with decreased elastic tissue
MONDO:0041447	metastatic malignant neoplasm in the colon
MONDO:0016436	acquired dermis elastic tissue disorder with increased elastic tissue
MONDO:0041448	metastasis from malignant tumor of colon
MONDO:0016437	late-onset focal dermal elastosis
MONDO:0016430	Balo concentric sclerosis
MONDO:0016431	autosomal dominant Charcot-Marie-Tooth disease type 2M
MONDO:0016432	heart-hand syndrome
MONDO:0016433	dysmorphism-short stature-deafness-disorder of sex development syndrome
MONDO:0016490	hemoglobin C-beta-thalassemia syndrome
MONDO:0016491	hemoglobin E-beta-thalassemia syndrome
MONDO:0016496	pharyngeal-cervical-brachial variant of Guillain-Barre syndrome
MONDO:0016497	paraparetic variant of Guillain-Barre syndrome
MONDO:0016498	acute pure sensory neuropathy
MONDO:0016499	acute pandysautonomia
MONDO:0016492	beta-thalassemia with other manifestations
MONDO:0016493	variant of Guillain-Barre syndrome
MONDO:0016494	regional variant of Guillain-Barre syndrome
MONDO:0016495	functional variant of Guillain-Barre syndrome
MONDO:0016480	silver-Russell syndrome due to an imprinting defect of 11p15
MONDO:0004499	lung hilum carcinoma
MONDO:0004496	myocarditis
MONDO:0004495	myotonic cataract
MONDO:0004498	sacral spinal canal and spinal cord meningioma
MONDO:0004497	tertiary syphilis
MONDO:0004492	mediastinitis
MONDO:0004491	uterine corpus choriocarcinoma
MONDO:0004494	testicular yolk sac tumor, hepatoid pattern
MONDO:0004493	testicular yolk sac tumor, papillary pattern
MONDO:0004490	gestational uterine corpus choriocarcinoma
MONDO:0016489	delta-beta-thalassemia
MONDO:0016485	Usher syndrome type 3
MONDO:0016486	beta-thalassemia major
MONDO:0016487	beta-thalassemia intermedia
MONDO:0016488	beta-thalassemia associated with another hemoglobin anomaly
MONDO:0016481	silver-Russell syndrome due to 11p15 microduplication
MONDO:0016482	silver-Russell syndrome due to maternal uniparental disomy of chromosome 11
MONDO:0016483	intracranial berry aneurysm
MONDO:0016484	Usher syndrome type 2
MONDO:0016478	Beckwith-Wiedemann syndrome due to 11p15 translocation/inversion
MONDO:0016479	silver-Russell syndrome due to 7p11.2p13 microduplication
MONDO:0041403	toxic amblyopia
MONDO:0016474	drug-induced lupus erythematosus
MONDO:0016475	Beckwith-Wiedemann syndrome due to imprinting defect of 11p15
MONDO:0016476	Beckwith-Wiedemann syndrome due to CDKN1C mutation
MONDO:0016477	Beckwith-Wiedemann syndrome due to 11p15 microdeletion
MONDO:0016470	Ehlers-Danlos/osteogenesis imperfecta syndrome
MONDO:0016471	pachyonychia congenita
MONDO:0016472	dracunculiasis
MONDO:0016473	familial rhabdoid tumor
MONDO:0004405	Barrett adenocarcinoma
MONDO:0004404	refractory precursor T-lymphoblastic lymphoma/leukemia
MONDO:0004407	stroma-dominant and stroma-poor composite ganglioneuroblastoma
MONDO:0004406	adult central nervous system mixed germ cell tumor
MONDO:0004401	testis refractory cancer
MONDO:0004400	malignant type A thymoma
MONDO:0004403	childhood precursor T-lymphoblastic lymphoma/leukemia
MONDO:0004402	testicular yolk sac tumor, glandular-alveolar pattern
MONDO:0004438	sporadic breast cancer
MONDO:0004437	gastric signet ring cell adenocarcinoma
MONDO:0004439	periocular meningioma
MONDO:0004434	glomangiomyoma
MONDO:0004433	papillary carcinoma of the penis
MONDO:0004436	ovarian myxoid liposarcoma
MONDO:0004435	liver fibrosarcoma
MONDO:0004430	penis mixed squamous cell carcinoma
MONDO:0004432	mature pericardial teratoma
MONDO:0004431	hemarthrosis
MONDO:0016427	coccidioidomycosis
MONDO:0016428	multiple sclerosis variant
MONDO:0016429	Marburg acute multiple sclerosis
MONDO:0016423	autoimmune polyendocrinopathy type 4
MONDO:0016424	progressive sensorineural hearing loss-hypertrophic cardiomyopathy syndrome
MONDO:0016425	Hughes-Stovin syndrome
MONDO:0016426	fusariosis
MONDO:0016420	familial flecked retinopathy
MONDO:0016421	toxic oil syndrome
MONDO:0016422	autoimmune polyendocrinopathy type 3
MONDO:0004449	intraductal breast myoepitheliosis
MONDO:0004448	frontal sinus inverted papilloma
MONDO:0004445	bladder papillary clear cell adenocarcinoma
MONDO:0004444	bladder tubulo-cystic clear cell adenocarcinoma
MONDO:0004447	pituitary stalk meningioma
MONDO:0004446	olfactory groove meningioma
MONDO:0004441	childhood ovarian embryonal carcinoma
MONDO:0004440	pineal region meningioma
MONDO:0004443	chest wall parachordoma
MONDO:0004442	testis polyembryoma
MONDO:0016409	primary congenital hypothyroidism
MONDO:0016416	diphallia
MONDO:0016417	congenital ichthyosis-microcephalus-tetraplegia syndrome
MONDO:0016418	multiple system atrophy, cerebellar type
MONDO:0016419	hereditary breast carcinoma
MONDO:0016412	peripheral hypothyroidism
MONDO:0016413	congenital hypothyroidism due to maternal intake of antithyroid drugs
MONDO:0016414	hypotrichosis-intellectual disability, Lopes type
MONDO:0016415	immunodeficiency-centromeric instability-facial anomalies syndrome
MONDO:0016410	central congenital hypothyroidism
MONDO:0016411	hypothyroidism due to deficient transcription factors involved in pituitary development or function
MONDO:0004416	plasmacytoid variant infiltrating bladder urothelial carcinoma
MONDO:0004415	lipid-cell variant infiltrating bladder urothelial carcinoma
MONDO:0004418	microcystic variant infiltrating bladder urothelial carcinoma
MONDO:0004417	nested variant infiltrating bladder urothelial carcinoma
MONDO:0004412	malignant spiradenoma
MONDO:0004411	duodenal gastrin-producing neuroendocrine tumor
MONDO:0004414	tamoxifen-related endometrial lesion
MONDO:0004413	cervical non-keratinizing squamous cell carcinoma
MONDO:0004410	sarcomatoid penile squamous cell carcinoma
MONDO:0016405	sterol metabolism disorder with epilepsy
MONDO:0016406	other metabolic disease with epilepsy
MONDO:0016407	oligomeganephronia
MONDO:0016408	permanent congenital hypothyroidism
MONDO:0016401	energy metabolism disorder with epilepsy
MONDO:0016402	mitochondrial disease with epilepsy
MONDO:0016403	mitochondrial disease with peripheral neuropathy
MONDO:0016404	metabolic neurotransmission anomaly with epilepsy
MONDO:0016400	metal transport or utilization disorder with epilepsy
MONDO:0004409	nipple duct carcinoma
MONDO:0004408	schwannian stroma-rich and stroma-poor composite ganglioneuroblastoma
MONDO:0004427	supraglottis neoplasm
MONDO:0004426	frontal convexity meningioma
MONDO:0004429	skin meningioma
MONDO:0004428	alveoli adenoma
MONDO:0004423	central nervous system extraskeletal osteosarcoma
MONDO:0004422	cerebral falx meningioma
MONDO:0004425	hyperthyroidism
MONDO:0004424	familial glomangioma
MONDO:0004421	sclerosing breast papilloma
MONDO:0004420	breast malignant eccrine spiradenoma
MONDO:0004419	lymphoma-like variant infiltrating bladder urothelial carcinoma
MONDO:0100160	alcoholic ketoacidosis
MONDO:0100161	hyperkalemic renal tubular acidosis
MONDO:0100163	COVID-19–associated multisystem inflammatory syndrome in children
MONDO:0100164	permanent neonatal diabetes mellitus
MONDO:0100165	permanent neonatal diabetes mellitus 1
MONDO:0100172	intellectual disability, autosomal dominant
MONDO:0100175	TTN-related myopathy
MONDO:0100176	AP-4 deficiency syndrome
MONDO:0100184	GTP cyclohydrolase I deficiency
MONDO:0100185	immune reconstitution inflammatory syndrome
MONDO:0100186	GTP cyclohydrolase I deficiency with hyperphenylalaninemia
MONDO:0100188	combined ApoA-I and ApoC-III deficiency
MONDO:0100189	apolipoprotein A-I deficiency
MONDO:0100192	liver failure
MONDO:0100193	chronic liver failure
MONDO:0100194	pregnancy associated osteoporosis
MONDO:0100195	X-linked intellectual disability with hypopituitarism
MONDO:0100196	TPM2-related myopathy
MONDO:0100197	parainfluenza infectious disease
MONDO:0006903	peroneal nerve paralysis
MONDO:0006904	phimosis
MONDO:0006901	peritoneal neoplasm
MONDO:0006902	periventricular leukomalacia
MONDO:0006900	perinephritis
MONDO:0041261	disorder of acid-base balance
MONDO:0041259	diphtheritic myocarditis
MONDO:0016290	Hernández-Aguirre Negrete syndrome
MONDO:0016291	craniosynostosis, Herrmann-Opitz type
MONDO:0016292	nodular neuronal heterotopia
MONDO:0016293	congenital stationary night blindness
MONDO:0016298	postlingual non-syndromic genetic deafness
MONDO:0016299	holoprosencephaly-caudal dysgenesis syndrome
MONDO:0016294	Hirschsprung disease-type D brachydactyly syndrome
MONDO:0016295	neuronal ceroid lipofuscinosis
MONDO:0016296	holoprosencephaly
MONDO:0016297	prelingual non-syndromic genetic deafness
MONDO:0016280	sarcoma of cervix uteri
MONDO:0016281	46,XX ovotesticular disorder of sex development
MONDO:0016282	rhabdomyosarcoma of the cervix uteri
MONDO:0100100	SELENON-related myopathy
MONDO:0004298	stomach disease
MONDO:0100101	fetal akinesia deformation sequence 1
MONDO:0004297	lymphoepithelioma-like thymic carcinoma
MONDO:0100102	fetal akinesia deformation sequence 2
MONDO:0100103	fetal akinesia deformation sequence 3
MONDO:0004299	infiltrating bladder lymphoepithelioma-like carcinoma
MONDO:0004294	gestational ovarian choriocarcinoma
MONDO:0100104	fetal akinesia deformation sequence 4
MONDO:0004293	supraglottis squamous cell carcinoma
MONDO:0041284	primary motor cortex epilepsy
MONDO:0100105	brain small vessel disease 3
MONDO:0004296	cervical lymphoepithelioma-like carcinoma
MONDO:0100106	neonatal epileptic encephalopathy
MONDO:0004295	asbestos-related lung carcinoma
MONDO:0100107	non-neonatal early infantile epileptic encephalopathy
MONDO:0004290	subglottis verrucous carcinoma
MONDO:0004292	supraglottis verrucous carcinoma
MONDO:0004291	subglottis squamous cell carcinoma
MONDO:0016287	adenoid basal carcinoma of the cervix uteri
MONDO:0016288	glassy cell carcinoma of the cervix uteri
MONDO:0016289	malignant germ cell tumor of cervix uteri
MONDO:0016283	leiomyosarcoma of the cervix uteri
MONDO:0016284	primitive neuroectodermal tumor of the cervix uteri
MONDO:0016285	papillary carcinoma of the cervix uteri
MONDO:0016286	adenoid cystic carcinoma of the cervix uteri
MONDO:0016270	low-grade neuroendocrine tumor of the corpus uteri
MONDO:0016271	adenoid cystic carcinoma of the corpus uteri
MONDO:0100110	adenovirus renal infection
MONDO:0100111	focal segmental glomerulosclerosis and neurodevelopmental syndrome
MONDO:0100112	acyl-CoA binding domain containing protein 5 deficiency
MONDO:0100113	hearing loss with skin disease
MONDO:0100114	dry age related macular degeneration
MONDO:0100115	acute flaccid myelitis
MONDO:0100116	Middle East respiratory syndrome
MONDO:0041295	acute papillary necrosis
MONDO:0100108	TPM3-related myopathy
MONDO:0100109	Zinner syndrome
MONDO:0016276	high-grade neuroendocrine carcinoma of the cervix uteri
MONDO:0016277	malignant mixed epithelial and mesenchymal tumor of cervix uteri
MONDO:0016278	carcinosarcoma of the cervix uteri
MONDO:0016279	adenosarcoma of the cervix uteri
MONDO:0016272	transitional cell carcinoma of the corpus uteri
MONDO:0016273	malignant germ cell tumor of corpus uteri
MONDO:0016274	rare cancer of cervix uteri
MONDO:0016275	adenocarcinoma of cervix uteri
MONDO:0100120	vector-borne disease
MONDO:0100121	SCN4A-related myopathy, autosomal recessive
MONDO:0100124	NAA10-related syndrome
MONDO:0043885	eye infectious disease
MONDO:0100125	hallucinogen-persisting perception disorder
MONDO:0100126	P5CS deficiency
MONDO:0100128	coinfection
MONDO:0043881	acute eosinophilic leukemia
MONDO:0100129	intracranial arachoid cyst
MONDO:0043878	hereditary optic atrophy
MONDO:0100130	adult acute respiratory distress syndrome
MONDO:0100131	pediatric acute respiratory distress syndrome
MONDO:0100132	intrahepatic bile duct adenosquamous carcinoma
MONDO:0043895	ankle injury
MONDO:0100133	mitochondrial complex I deficiency
MONDO:0100134	mitochondrial complex I deficiency, mitochondrial type
MONDO:0100135	Dravet syndrome
MONDO:0100136	Fanconia anemia complementation group M
MONDO:0100137	telomere syndrome
MONDO:0100138	X-linked recessive mitochondrial myopathy
MONDO:0100139	asymptomatic COVID-19 infection
MONDO:0043892	prosthesis-related infectious disease
MONDO:0100140	mild COVID-19 infection
MONDO:0100141	moderate COVID-19 infection
MONDO:0100142	severe COVID-19 infection
MONDO:0100143	critical COVID-19 infection
MONDO:0100144	Uner Tan Syndrome
MONDO:0100145	presymptomatic COVID-19 infection
MONDO:0100146	ATP6AP2-related disorder
MONDO:0100147	SATB2 associated disorder
MONDO:0100148	X-linked complex neurodevelopmental disorder
MONDO:0100150	RYR1-related myopathy
MONDO:0100151	nephropathic cystinosis
MONDO:0100152	DKC1-related disorder
MONDO:0100156	Imerslund-Grasbeck syndrome type 1
MONDO:0100157	Imerslund-Grasbeck syndrome type 2
MONDO:0004357	carcinoma of supraglottis
MONDO:0004356	childhood multilocular cystic kidney neoplasm
MONDO:0004359	delusional disorder
MONDO:0004358	subglottis carcinoma
MONDO:0004353	extrahepatic biliary papillomatosis
MONDO:0004352	adult brain ependymoma
MONDO:0004355	childhood leukemia
MONDO:0004354	neonatal leukemia
MONDO:0004351	intraocular lymphoma
MONDO:0004350	pediatric extraocular retinoblastoma
MONDO:0043959	pseudolymphoma
MONDO:0016346	hydrocephalus-obesity-hypogonadism syndrome
MONDO:0016347	rare cardiac rhythm disease
MONDO:0043953	burkholderia infectious disease
MONDO:0016348	non-genetic cardiac rhythm disease
MONDO:0016349	congenital hydrocephalus
MONDO:0016342	familial isolated arrhythmogenic right ventricular dysplasia
MONDO:0016343	unclassified cardiomyopathy
MONDO:0016344	hydranencephaly
MONDO:0016345	non-familial restrictive cardiomyopathy
MONDO:0016340	familial restrictive cardiomyopathy
MONDO:0016341	lysosomal disease with restrictive cardiomyopathy
MONDO:0004368	sphenoorbital meningioma
MONDO:0004367	petroclival meningioma
MONDO:0004369	renal infectious disease
MONDO:0004364	choroid necrotic melanoma
MONDO:0004363	adult spinal cord glioblastoma
MONDO:0004366	mixed astrocytoma-ependymoma-oligodendroglioma
MONDO:0004365	necrotic uveal melanoma
MONDO:0004360	breast extraskeletal osteosarcoma
MONDO:0004362	placenta disease
MONDO:0004361	adult spinal cord ependymoma
MONDO:0043969	nocturnal paroxysmal dystonia
MONDO:0016339	restrictive cardiomyopathy
MONDO:0018998	Leber congenital amaurosis
MONDO:0016335	mitochondrial disease with dilated cardiomyopathy
MONDO:0018997	Noonan syndrome
MONDO:0016336	fatty acid oxidation and ketogenesis disorder with dilated cardiomyopathy
MONDO:0016337	syndrome associated with dilated cardiomyopathy
MONDO:0018999	LCAT deficiency
MONDO:0016338	non-familial dilated cardiomyopathy
MONDO:0018994	Charcot-Marie-Tooth disease type X
MONDO:0016331	infantile systemic hyalinosis
MONDO:0016332	hypertrophic cardiomyopathy due to intensive athletic training
MONDO:0018993	Charcot-Marie-Tooth disease type 2
MONDO:0018996	spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 2
MONDO:0016333	familial dilated cardiomyopathy
MONDO:0018995	Charcot-Marie-Tooth disease type 4
MONDO:0016334	neuromuscular disease with dilated cardiomyopathy
MONDO:0018990	pulmonary blastoma
MONDO:0018992	IgG4-related thyroid disease
MONDO:0018991	hepatoportal sclerosis
MONDO:0016330	non-familial hypertrophic cardiomyopathy
MONDO:0004339	tuberculum sellae meningioma
MONDO:0004338	retinal cell cancer
MONDO:0006998	tonsil cancer
MONDO:0004335	digestive system disease
MONDO:0004334	non-functional pancreatic neuroendocrine tumor
MONDO:0006999	tooth disease
MONDO:0004337	perianal skin Paget disease
MONDO:0006996	thyroid crisis
MONDO:0006997	tibial neuropathy
MONDO:0004336	rectal signet ring cell adenocarcinoma
MONDO:0004331	bladder urachal adenocarcinoma
MONDO:0006994	tarsal tunnel syndrome
MONDO:0004330	leptomeningeal sarcoma
MONDO:0043982	cubital tunnel syndrome
MONDO:0006995	tethered spinal cord syndrome
MONDO:0043985	central nervous system lupus
MONDO:0006992	syphilitic aortitis
MONDO:0004333	pancreatic ACTH-producing neuroendocrine tumor
MONDO:0004332	lung hilum cancer
MONDO:0006993	systolic heart failure
MONDO:0006990	suppurative uveitis
MONDO:0006991	sympathetic ophthalmia
MONDO:0016328	fatty acid oxidation and ketogenesis disorder with hypertrophic cardiomyopathy
MONDO:0016329	familial syndrome associated with hypertrophic cardiomyopathy
MONDO:0018987	granulomatous mastitis
MONDO:0016324	hypertrophic cardiomyopathy
MONDO:0043975	autonomic dysreflexia
MONDO:0016325	glycogen storage disease with hypertrophic cardiomyopathy
MONDO:0018986	leiomyosarcoma
MONDO:0018989	recurrent acute pancreatitis
MONDO:0016326	lysosomal disease with hypertrophic cardiomyopathy
MONDO:0016327	mitochondrial disease with hypertrophic cardiomyopathy
MONDO:0018988	iridocorneal endothelial syndrome
MONDO:0018983	tolosa-Hunt syndrome
MONDO:0016320	rare hereditary thrombophilia
MONDO:0016321	pulmonary interstitial glycogenosis
MONDO:0018982	Niemann-Pick disease type C
MONDO:0016322	neuroendocrine cell hyperplasia of infancy
MONDO:0018985	trench fever
MONDO:0016323	chronic respiratory distress with surfactant metabolism deficiency
MONDO:0018984	Oroya fever
MONDO:0018981	benign idiopathic neonatal seizures
MONDO:0018980	acrofacial dysostosis, Kennedy-Teebi type
MONDO:0004349	retina lymphoma
MONDO:0004346	signet ring cell intrahepatic cholangiocarcinoma
MONDO:0004345	childhood malignant schwannoma
MONDO:0004348	retinal telangiectasia
MONDO:0043994	acute cholecystitis
MONDO:0004342	osteoclast-like giant cell neoplasm of the pancreas
MONDO:0004341	colloid carcinoma of the pancreas
MONDO:0004344	childhood malignant hemangiopericytoma
MONDO:0004343	pancreatic acinar cell cystadenocarcinoma
MONDO:0004340	mixed ductal-endocrine carcinoma of pancreas
MONDO:0016317	limbic encephalitis with NMDA receptor antibodies
MONDO:0016318	progressive multifocal leukoencephalopathy
MONDO:0018979	multifocal motor neuropathy
MONDO:0016319	congenital insensitivity to pain with hyperhidrosis
MONDO:0018976	schisis association
MONDO:0016313	renal cell carcinoma
MONDO:0016314	rare carcinoma of pancreas
MONDO:0018975	neurofibromatosis type 1
MONDO:0016315	mucopolysaccharidosis type 2, severe form
MONDO:0018978	IgG4-related mediastinitis
MONDO:0018977	polyneuropathy associated with IgM monoclonal gammapathy with anti-MAG
MONDO:0016316	mucopolysaccharidosis type 2, attenuated form
MONDO:0043988	zoster sine herpete
MONDO:0018972	rare epithelial tumor of stomach
MONDO:0016310	Niemann-Pick disease type C, adult neurologic onset
MONDO:0018971	isolated oxycephaly
MONDO:0018974	paraneoplastic pemphigus
MONDO:0016311	Bockenheimer syndrome
MONDO:0018973	patterned dystrophy of the retinal pigment epithelium
MONDO:0016312	5-fluorouracil poisoning
MONDO:0018970	pemphigoid gestationis
MONDO:0016380	acquired hypertrichosis lanuginosa
MONDO:0016381	hypertrichosis lanuginosa congenita
MONDO:0004397	benign mediastinal psammomatous neurilemmoma
MONDO:0004396	cervical spinal canal and spinal cord meningioma
MONDO:0004399	epithelial malignant thymoma
MONDO:0004398	mediastinal schwannoma
MONDO:0004393	mixed astrocytoma-ependymoma
MONDO:0004392	intracranial extraskeletal myxoid chondrosarcoma
MONDO:0004395	mixed oligodendroglioma-astrocytoma
MONDO:0004394	maxillary sinus squamous cell carcinoma
MONDO:0004391	adult extraosseous chondrosarcoma
MONDO:0004390	ocular hypotension
MONDO:0016386	hypogonadotropic hypogonadism-retinitis pigmentosa syndrome
MONDO:0016387	mitochondrial oxidative phosphorylation disorder
MONDO:0016388	bone sarcoma
MONDO:0016389	lymphoma
MONDO:0016382	hereditary poikiloderma
MONDO:0016383	nephrogenic diabetes insipidus
MONDO:0016384	hypogonadotropic hypogonadism-frontoparietal alopecia syndrome
MONDO:0016385	hypogonadism-mitral valve prolapse-intellectual disability syndrome
MONDO:0043919	radiation pneumonitis
MONDO:0016370	Marchiafava-Bignami disease
MONDO:0016379	erosive pustular dermatosis of the scalp
MONDO:0043923	lichen planus, oral
MONDO:0016375	acquired peripheral movement disorder
MONDO:0016376	confetti-like macular atrophy
MONDO:0016377	Pitt-Hopkins-like syndrome
MONDO:0016378	maternal hyperthermia induced birth defects
MONDO:0016371	combined hyperactive dysfunction syndrome of the cranial nerves
MONDO:0016372	glossopharyngeal neuralgia
MONDO:0016373	isolated facial myokymia
MONDO:0016374	cranial neuralgia
MONDO:0004379	female breast carcinoma
MONDO:0004378	pediatric cerebral ependymoblastoma
MONDO:0004375	end stage renal failure
MONDO:0004374	adult extraskeletal osteosarcoma
MONDO:0004377	pancreatic non-functioning delta cell tumor
MONDO:0004376	infiltrating nipple syringomatous adenoma
MONDO:0004371	spinal multifocal clear cell meningioma
MONDO:0004370	sphenocavernous meningioma
MONDO:0004373	adult papillary meningioma
MONDO:0004372	chronic toxic polyneuropathy
MONDO:0016368	Rothmund-Thomson syndrome type 1
MONDO:0016369	Rothmund-Thomson syndrome type 2
MONDO:0016364	Joubert syndrome with ocular defect
MONDO:0016365	familial primary hyperparathyroidism
MONDO:0016366	maternal phenylketonuria
MONDO:0016367	dermatomyositis
MONDO:0016360	marcothrombocytopenia with mitral valve insufficiency
MONDO:0016361	isolated hereditary giant platelet disorder
MONDO:0016362	attenuated familial adenomatous polyposis
MONDO:0016363	rare hereditary hemochromatosis
MONDO:0004389	mite infestation
MONDO:0004386	uterine corpus atypical polypoid adenomyoma
MONDO:0004385	adult xanthogranuloma
MONDO:0004388	testicular spermatocytic seminoma
MONDO:0004387	luteoma of pregnancy
MONDO:0004382	laryngeal disease
MONDO:0004381	pancreatic intraductal papillary-mucinous neoplasm with low grade dysplasia
MONDO:0004384	maxillary sinus inverted papilloma
MONDO:0004383	adult central nervous system germinoma
MONDO:0004380	dendritic cell sarcoma
MONDO:0016357	dysplastic cortical hyperostosis
MONDO:0016358	limited cutaneous systemic sclerosis
MONDO:0016359	limited systemic sclerosis
MONDO:0016353	palmoplantar keratoderma-spastic paralysis syndrome
MONDO:0016354	xeroderma pigmentosum-Cockayne syndrome complex
MONDO:0016355	semilobar holoprosencephaly
MONDO:0016356	diffuse cutaneous systemic sclerosis
MONDO:0016350	hydrocephalus-blue sclerae-nephropathy syndrome
MONDO:0016351	anti-HLA hyperimmunization
MONDO:0016352	idiopathic inherited hypercalciuria
MONDO:0006936	pulmonary valve stenosis
MONDO:0006937	pulpitis
MONDO:0006935	pulmonary subvalvular stenosis
MONDO:0006932	pulmonary edema
MONDO:0006933	pulmonary plasma cell granuloma
MONDO:0006930	pseudobulbar palsy
MONDO:0006931	pulmonary coin lesion
MONDO:0018918	carcinoma of gallbladder and extrahepatic biliary tract
MONDO:0018917	Marfan syndrome
MONDO:0018919	McCune-Albright syndrome
MONDO:0018925	familial or sporadic hemiplegic migraine
MONDO:0018924	microphthalmia, Lenz type
MONDO:0018927	SUNCT syndrome
MONDO:0018926	human prion disease
MONDO:0018921	Meckel syndrome
MONDO:0018920	peripartum cardiomyopathy
MONDO:0018923	22q11.2 deletion syndrome
MONDO:0018922	cold agglutinin disease
MONDO:0006929	Proteus infectious disease
MONDO:0006927	Rickettsiaceae infectious disease
MONDO:0006928	proliferative vitreoretinopathy
MONDO:0006947	renovascular hypertension
MONDO:0006948	retinal artery occlusion
MONDO:0006945	renal artery obstruction
MONDO:0006946	renal osteodystrophy
MONDO:0006943	relapsing polychondritis
MONDO:0006944	renal aminoaciduria
MONDO:0006941	rat-bite fever
MONDO:0006942	reflex epilepsy
MONDO:0006940	radial nerve lesion
MONDO:0018907	craniopharyngioma
MONDO:0018906	follicular lymphoma
MONDO:0018909	legionellosis
MONDO:0018908	non-Hodgkin lymphoma
MONDO:0018914	hypotrichosis simplex
MONDO:0018913	malakoplakia
MONDO:0018916	isolated anorectal malformation
MONDO:0018915	pneumococcal meningitis
MONDO:0018910	oculocutaneous albinism
MONDO:0018912	Cushing syndrome
MONDO:0018911	maturity-onset diabetes of the young
MONDO:0006938	pyelitis
MONDO:0006939	pyelonephritis
MONDO:0006914	POEMS syndrome
MONDO:0006915	polyradiculoneuropathy
MONDO:0006912	pneumatosis cystoides intestinalis
MONDO:0006913	pneumococcal meningitis
MONDO:0006910	pituitary-dependent Cushing disease
MONDO:0006911	placental site trophoblastic tumor
MONDO:0018903	sarcocystosis
MONDO:0018902	hepatocellular adenoma
MONDO:0018905	diffuse large B-cell lymphoma
MONDO:0018904	primary membranoproliferative glomerulonephritis
MONDO:0018901	left ventricular noncompaction
MONDO:0018900	corticosteroid-sensitive aseptic abscess syndrome
MONDO:0006909	pituitary dwarfism
MONDO:0006907	pilar sheath acanthoma
MONDO:0006908	pituitary apoplexy
MONDO:0006905	pigmented spindle cell nevus
MONDO:0006906	pigmented villonodular synovitis
MONDO:0006925	Fusobacteriaceae infectious disease
MONDO:0006926	haemophilus infectious disease
MONDO:0006923	Bacillaceae infectious disease
MONDO:0006924	Bartonellaceae infectious disease
MONDO:0006921	Actinomycetales infectious disease
MONDO:0006922	Anaplasmataceae infectious disease
MONDO:0006920	prediabetes syndrome
MONDO:0043905	pneumonitis
MONDO:0043904	leishmaniasis, diffuse cutaneous
MONDO:0006918	posterior uveitis
MONDO:0006919	potassium deficiency
MONDO:0006916	postcholecystectomy syndrome
MONDO:0006917	posterior cerebral artery infarction
MONDO:0004317	multiple spinal canal and spinal cord meningioma
MONDO:0004316	acantholytic squamous cell skin carcinoma
MONDO:0006978	splenic infarction
MONDO:0004319	hypercalcemic type ovarian small cell carcinoma
MONDO:0004318	pulmonary type ovarian small cell carcinoma
MONDO:0006979	steatitis
MONDO:0006976	somatostatinoma
MONDO:0004313	gasserian ganglion meningioma
MONDO:0006977	spermatocele
MONDO:0004312	suprasellar meningioma
MONDO:0006974	small cell sarcoma
MONDO:0004315	cholangiolocellular carcinoma
MONDO:0006975	smooth muscle tumor
MONDO:0004314	malignant cutaneous granular cell skin tumor
MONDO:0006972	silo filler disease
MONDO:0006973	skin appendage carcinoma
MONDO:0004311	carcinoma of Cowper glands
MONDO:0006970	sialolithiasis
MONDO:0006971	sigmoid neoplasm
MONDO:0004310	adult embryonal tumor with multilayered rosettes, c19mc-altered
MONDO:0018969	craniorachischisis
MONDO:0016306	Niemann-Pick disease type C, severe perinatal form
MONDO:0018968	iniencephaly
MONDO:0016307	Niemann-Pick disease type C, severe early infantile neurologic onset
MONDO:0016308	Niemann-Pick disease type C, late infantile neurologic onset
MONDO:0016309	Niemann-Pick disease type C, juvenile neurologic onset
MONDO:0018965	Alport syndrome
MONDO:0016302	isolated congenitally uncorrected transposition of the great arteries
MONDO:0016303	congenitally uncorrected transposition of the great arteries with cardiac malformation
MONDO:0018964	homocystinuria without methylmalonic aciduria
MONDO:0016304	classic pantothenate kinase-associated neurodegeneration
MONDO:0018967	short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinemia
MONDO:0018966	isolated growth hormone deficiency
MONDO:0016305	atypical pantothenate kinase-associated neurodegeneration
MONDO:0018961	familial melanoma
MONDO:0018960	congenital primary megaureter
MONDO:0018963	hereditary methemoglobinemia
MONDO:0016300	transposition of the great arteries
MONDO:0016301	congenitally corrected transposition of the great arteries
MONDO:0018962	common mesentery
MONDO:0004309	sarcomatosis
MONDO:0004328	maxillary sinus adenocarcinoma
MONDO:0004327	sphenoid sinus Schneiderian papilloma
MONDO:0006989	suppurative periapical periodontitis
MONDO:0004329	pancreatic intraductal papillary-mucinous neoplasm with high grade dysplasia
MONDO:0004324	testicular fibroma
MONDO:0006987	subvalvular aortic stenosis
MONDO:0006988	sulfhemoglobinemia
MONDO:0004323	muscular atrophy
MONDO:0004326	sphenoid sinus inverted papilloma
MONDO:0006985	subependymoma
MONDO:0006986	substernal goiter
MONDO:0004325	testicular thecoma
MONDO:0006983	subclavian steal syndrome
MONDO:0004320	adult infiltrating astrocytic neoplasm
MONDO:0006984	subdural empyema
MONDO:0006981	subacute bacterial endocarditis
MONDO:0004322	non-gestational ovarian choriocarcinoma
MONDO:0006982	subacute thyroiditis
MONDO:0004321	endometrial mixed adenocarcinoma
MONDO:0006980	struma ovarii
MONDO:0018958	nemaline myopathy
MONDO:0018957	pudendal neuralgia
MONDO:0018959	potassium-aggravated myotonia
MONDO:0018954	Loeys-Dietz syndrome
MONDO:0018953	parietal foramina
MONDO:0018956	idiopathic bronchiectasis
MONDO:0018955	recurrent respiratory papillomatosis
MONDO:0018950	3-methylcrotonyl-CoA carboxylase deficiency
MONDO:0018952	argyria
MONDO:0018951	distal myopathy with vocal cord weakness
MONDO:0006958	SAPHO syndrome
MONDO:0006959	Schnitzler syndrome
MONDO:0006956	Rickettsiosis
MONDO:0006957	root caries
MONDO:0006954	rheumatic fever
MONDO:0006955	rheumatic heart disease
MONDO:0006952	retinopathy of prematurity
MONDO:0006953	Rh isoimmunization
MONDO:0006950	retinal vasculitis
MONDO:0006951	retinal vein occlusion
MONDO:0018939	muscle-eye-brain disease
MONDO:0018947	centronuclear myopathy
MONDO:0018946	rhombencephalosynapsis
MONDO:0018949	distal myopathy
MONDO:0018948	multiminicore myopathy
MONDO:0018943	myofibrillar myopathy
MONDO:0018942	macrophagic myofasciitis
MONDO:0018945	McLeod neuroacanthocytosis syndrome
MONDO:0018944	gestational trophoblastic neoplasm
MONDO:0018941	furuncular myiasis
MONDO:0018940	congenital myasthenic syndrome
MONDO:0006949	retinal drusen
MONDO:0006969	sialadenitis
MONDO:0004306	childhood intracortical osteosarcoma
MONDO:0004305	parathyroid oncocytic adenoma
MONDO:0006967	septic abortion
MONDO:0004308	meningeal sarcoma
MONDO:0006968	shoulder impingement syndrome
MONDO:0004307	sarcomatosis of the meninges
MONDO:0004302	chief cell adenoma
MONDO:0006965	secondary hypertrophic osteoarthropathy
MONDO:0006966	secondary Parkinson disease
MONDO:0004301	fibrosarcomatous osteosarcoma
MONDO:0006963	sebaceous gland neoplasm
MONDO:0004304	mixed cell type adenoma of parathyroid
MONDO:0006964	secondary hyperparathyroidism
MONDO:0004303	parathyroid gland clear cell adenoma
MONDO:0006961	scrapie
MONDO:0006962	sebaceous adenocarcinoma
MONDO:0004300	intracortical osteogenic sarcoma
MONDO:0006960	sciatic neuropathy
MONDO:0018929	medial condensing osteitis of the clavicle
MONDO:0018928	rare hepatic disease
MONDO:0018936	osteoblastoma
MONDO:0018935	hairy cell leukemia
MONDO:0018938	mucopolysaccharidosis type 4
MONDO:0018937	mucopolysaccharidosis type 3
MONDO:0018932	cirrhotic cardiomyopathy
MONDO:0018931	mucolipidosis type III
MONDO:0018934	mucopolysaccharidosis type 1
MONDO:0018933	Mazabraud syndrome
MONDO:0018930	monosomy 21
MONDO:0100040	FOXG1 disorder
MONDO:0100041	secondary trimethylaminuria
MONDO:0100044	acrofrontofacionasal dysostosis 1
MONDO:0100050	Usher syndrome, type 1D/F
MONDO:0100051	idiopathic mast cell activation syndrome
MONDO:0100052	acetazolamide-responsive hereditary episodic ataxia
MONDO:0100053	anaphylaxis
MONDO:0100054	idiopathic anaphylaxis
MONDO:0100055	intraosseous spindle cell rhabdomyosarcoma with TFCP2/NCOA2 rearrangements
MONDO:0100056	exercise-induced anaphylaxis
MONDO:0100057	food-dependent exercise-induced anaphylaxis
MONDO:0100058	hypervalinemia and hyperleucine-isoleucinemia
MONDO:0100059	hypereosinophilia of undetermined significance
MONDO:0100060	congenital/infantile spindle cell rhabdomyosarcoma with VGLL2/NCOA2/CITED2 rearrangements
MONDO:0100061	PRPS1 deficiency disorder
MONDO:0100062	developmental and epileptic encephalopathy
MONDO:0100063	Pericytoma with t(7;12)
MONDO:0100064	tyrosine hydroxylase deficiency
MONDO:0100065	TH-deficient infantile parkinsonism and motor delay
MONDO:0100066	TH-deficient progressive infantile encephalopathy
MONDO:0100067	childhood spindle cell rhabdomyosarcoma
MONDO:0100068	SLC10A7-CDG
MONDO:0100069	hearing impairment and infertile male syndrome
MONDO:0100070	neuroendocrine disease
MONDO:0100071	cardiocutaneous syndrome
MONDO:0100072	neonatal diabetes, congenital sensorineural hearing loss and congenital cataracts
MONDO:0100073	methicillin-resistant staphylococcus aureus infectious disease
MONDO:0100074	norovirus infectious disease
MONDO:0100075	jaw fracture
MONDO:0100076	juvenile idiopathic scoliosis
MONDO:0100077	congenital alveolar dysplasia
MONDO:0100078	resistant hypertension
MONDO:0100079	developmental and epileptic encephalopathy, 6
MONDO:0100081	sleep disorder
MONDO:0100082	LEOPARD syndrome 1
MONDO:0041182	polymorphic light eruption
MONDO:0100083	hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1
MONDO:0100084	alpha-actinopathy
MONDO:0100085	cancer of long bone of upper limb
MONDO:0100086	perinatal disease
MONDO:0100087	familial Alzheimer disease
MONDO:0100088	late-onset familial alzheimer disease
MONDO:0100089	GATA1-Related X-Linked Cytopenia
MONDO:0041186	Rowell syndrome
MONDO:0100080	cardioectodermal syndrome
MONDO:0100092	myoclonus, familial, 2
MONDO:0100093	myoclonus, familial, 1
MONDO:0100094	cannabinoid hyperemesis syndrome
MONDO:0100095	neurodegeneration, childhood-onset, stress-induced, with variable ataxia and seizures
MONDO:0100096	COVID-19
MONDO:0100097	congenital alveolar dysplasia due to TBX4
MONDO:0100099	retrograde cricopharyngeus dysfunction
MONDO:0100090	congenital alveolar dysplasia due to FGF10
MONDO:0100091	inherited pseudoxanthoma elasticum
MONDO:0016180	hematological disease associated with an acquired peripheral neuropathy
MONDO:0016181	solid tumor associated with an acquired peripheral neuropathy
MONDO:0016182	qualitative or quantitative defects of protein O-mannose beta1,2N-acetylglucosaminyltransferase
MONDO:0016183	qualitative or quantitative defects of protein glycosyltransferase-like
MONDO:0004199	vulvar keratinizing squamous cell carcinoma
MONDO:0004198	testicular yolk sac tumor, solid pattern
MONDO:0004195	thymic dysplasia
MONDO:0004194	ovarian stromal hyperthecosis
MONDO:0004197	male urethral cancer
MONDO:0004196	rectal sarcomatoid carcinoma
MONDO:0004191	nephrogenic adenoma
MONDO:0004190	nephrogenic adenoma of urinary bladder
MONDO:0004193	pediatric ovarian dysgerminoma
MONDO:0004192	urethra cancer
MONDO:0016188	qualitative or quantitative defects of alphaB-cristallin
MONDO:0016189	qualitative or quantitative defects of filamin C
MONDO:0016184	qualitative or quantitative defects of protein O-mannosyltransferase 1
MONDO:0016185	qualitative or quantitative defects of protein O-mannosyltransferase 2
MONDO:0016186	qualitative or quantitative defects of myofibrillar proteins
MONDO:0016187	qualitative or quantitative defects of desmin
MONDO:0016170	chronic polyradiculoneuropathy
MONDO:0016171	polyradiculoneuropathy associated with IgG/IgA/IgM monoclonal gammopathy without known antibodies
MONDO:0016172	acquired sensory ganglionopathy
MONDO:0041154	disease of neck of urinary bladder
MONDO:0016177	systemic inflammatory disease associated with an acquired peripheral neuropathy
MONDO:0016178	peripheral neuropathy associated with monoclonal gammopathy
MONDO:0016179	acquired amyloid peripheral neuropathy
MONDO:0016173	non-paraneoplastic sensory ganglionopathy
MONDO:0016174	paraneoplastic sensory ganglionopathy
MONDO:0016175	cutis laxa
MONDO:0016176	axonal polyneuropathy associated with IgG/IgM/IgA monoclonal gammopathy
MONDO:0016160	X-linked intellectual disability-epilepsy syndrome
MONDO:0016161	cerebral gigantism-jaw cysts syndrome
MONDO:0041161	endometrial hyperplasia
MONDO:0004177	benign urethral neoplasm
MONDO:0004176	childhood extraosseous osteosarcoma
MONDO:0041167	carcinoid crisis
MONDO:0004179	astroblastoma
MONDO:0004178	testicular yolk sac tumor, endodermal sinus pattern
MONDO:0004173	adenocarcinoma of skene gland origin
MONDO:0004172	uterine corpus adenocarcinofibroma
MONDO:0004175	mucin-rich endometrial endometrioid adenocarcinoma
MONDO:0004174	secretory uterine corpus endometrioid adenocarcinoma
MONDO:0004171	congenital epulis
MONDO:0004170	nodular episcleritis
MONDO:0016166	genetic hyperparathyroidism
MONDO:0016167	optic pathway glioma
MONDO:0016168	cryopyrin-associated periodic syndrome
MONDO:0016169	chronic acquired demyelinating polyneuropathy
MONDO:0016162	bilateral frontal polymicrogyria
MONDO:0016163	autosomal dominant cerebellar ataxia type II
MONDO:0016164	herpetiform pemphigus
MONDO:0016165	genetic hypoparathyroidism
MONDO:0016150	qualitative or quantitative defects of integrin alpha-7
MONDO:0004188	iris spindle cell melanoma
MONDO:0004187	nodular fasciitis
MONDO:0004189	esophageal tuberculosis
MONDO:0004184	urethral disease
MONDO:0004183	axonal neuropathy
MONDO:0004186	cranial nodular fasciitis
MONDO:0004185	ovarian serous cystadenofibroma
MONDO:0004180	benign urinary system neoplasm
MONDO:0004182	stage IVb bladder cancer
MONDO:0004181	breast adenomyoepithelial adenosis
MONDO:0016159	Gemignani syndrome
MONDO:0016155	qualitative or quantitative defects of protein involved in O-glycosylation of alpha-dystroglycan
MONDO:0016156	qualitative or quantitative defects of FKRP
MONDO:0016157	qualitative or quantitative defects of fukutin
MONDO:0016158	narcolepsy-cataplexy syndrome
MONDO:0016151	qualitative or quantitative defects of perlecan
MONDO:0016152	qualitative or quantitative defects of calpain
MONDO:0016153	qualitative or quantitative defects of TRIM32
MONDO:0016154	qualitative or quantitative defects of myotubularin
MONDO:0100000	MED12-related intellectual disability syndrome
MONDO:0100001	alpha-gal syndrome
MONDO:0043762	tubal pregnancy
MONDO:0100002	food protein-induced allergic proctocolitis
MONDO:0100003	susceptibility to angioedema induced by ACE inhibitors
MONDO:0043765	presbycusis
MONDO:0100004	mast cell activation syndrome
MONDO:0100005	primary mast cell activation syndrome
MONDO:0100006	secondary mast cell activation syndrome
MONDO:0100007	chronic inflammatory demyelinating polyneuropathy
MONDO:0100008	food protein-induced enterocolitis syndrome
MONDO:0043759	abdominal ectopic pregnancy
MONDO:0100010	tendinopathy
MONDO:0100011	tendinosis
MONDO:0100012	paratenonitis
MONDO:0100013	paratenonitis with tendinosis
MONDO:0100014	autoimmune retinopathy
MONDO:0041114	peripheral ischemia
MONDO:0100015	adult-onset segmental dystonia
MONDO:0043775	respiratory paralysis
MONDO:0100016	early-onset generalized dystonia
MONDO:0100017	pityriasis rubra pilaris
MONDO:0100018	adult onset pityriasis rubra pilaris
MONDO:0043771	radiodermatitis
MONDO:0100019	ECHS1-related paroxysmal dyskinesia
MONDO:0043768	thrombocytopenic purpura
MONDO:0100020	atypical childhood epilepsy with centrotemporal spikes
MONDO:0100021	photosensitive occipital lobe epilepsy
MONDO:0100022	neonatal/infantile epilepsy syndrome
MONDO:0100023	self-limited familial and non-familial neonatal seizures
MONDO:0100024	self-limited familial and non-familial infantile seizures
MONDO:0100025	epilepsy of infancy with migrating focal seizures
MONDO:0043786	serositis
MONDO:0100026	myoclonic encephalopathy in non-progressive disorder
MONDO:0100027	febrile seizures plus, genetic epilepsy with febrile seizures plus
MONDO:0100028	immune epilepsy
MONDO:0043783	sclerema neonatorum
MONDO:0100029	antibody mediated epilepsy
MONDO:0043777	rhinophyma
MONDO:0016191	qualitative or quantitative defects of titin
MONDO:0016192	qualitative or quantitative defects of telethonin
MONDO:0016193	qualitative or quantitative defects of alpha-actin
MONDO:0016194	qualitative or quantitative defects of nebulin
MONDO:0100030	adolescent/adult-onset epilepsy syndrome
MONDO:0100031	adolescent/adult onset autosomal dominant epilepsy with auditory features
MONDO:0100032	familial temporal lobe epilepsy syndrome
MONDO:0100033	metabolic epilepsy
MONDO:0016190	qualitative or quantitative defects of protein ZASP
MONDO:0100034	cerebral folate deficiency
MONDO:0100035	structural epilepsy
MONDO:0100036	variable age onset epilepsy
MONDO:0043797	spinal cord injury
MONDO:0100037	juvenile onset pityriasis rubra pilaris
MONDO:0100038	complex neurodevelopmental disorder
MONDO:0100039	CDKL5 disorder
MONDO:0043789	serum sickness
MONDO:0016199	qualitative or quantitative defects of protein SERCA1
MONDO:0016195	qualitative or quantitative defects of beta-myosin heavy chain (MYH7)
MONDO:0016196	qualitative or quantitative defects of emerin
MONDO:0016197	qualitative or quantitative defects of selenoprotein N1
MONDO:0016198	qualitative or quantitative defects of plectin
MONDO:0004239	cervical keratinizing squamous cell carcinoma
MONDO:0004236	duodenal somatostatinoma
MONDO:0006899	pericoronitis
MONDO:0004235	diverticulitis
MONDO:0006897	periapical granuloma
MONDO:0004238	petrous apex meningioma
MONDO:0006898	periarthritis
MONDO:0004237	large cell carcinoma with rhabdoid phenotype
MONDO:0006895	penile neoplasm
MONDO:0004232	large cell keratinizing variant squamous cell breast carcinoma
MONDO:0004231	spindle cell variant squamous cell breast carcinoma
MONDO:0006896	peptic esophagitis
MONDO:0004234	chronic lymphoproliferative disorder of NK-cells
MONDO:0006893	Pasteurella hemorrhagic septicemia
MONDO:0004233	childhood pleomorphic rhabdomyosarcoma
MONDO:0006894	patellofemoral pain syndrome
MONDO:0006891	partial motor epilepsy
MONDO:0006892	partial sensory epilepsy
MONDO:0004230	adenomatoid tumor
MONDO:0006890	parathyroid gland adenoma
MONDO:0016229	genetic vascular anomaly
MONDO:0043836	tuberculosis, spinal
MONDO:0043839	ulcer disease
MONDO:0018888	congenital cornea plana
MONDO:0016225	specific learning disability
MONDO:0018887	rare cutaneous lupus erythematosus
MONDO:0016226	specific language disorder
MONDO:0016227	hereditary episodic ataxia
MONDO:0016228	rare vascular tumor
MONDO:0018889	hyaline body myopathy
MONDO:0018884	Roch-Leri mesosomatous lipomatosis
MONDO:0016221	temporomandibular joint anomaly
MONDO:0018883	Berardinelli-Seip congenital lipodystrophy
MONDO:0016222	spindle cell hemangioma
MONDO:0018886	listeriosis
MONDO:0016223	infantile hemangioma of rare localization
MONDO:0018885	orbital leiomyoma
MONDO:0016224	autosomal dominant proximal spinal muscular atrophy
MONDO:0018880	rare teratologic disease
MONDO:0018882	vasculitis
MONDO:0018881	myelodysplastic syndrome
MONDO:0016220	congenital temporomandibular joint ankylosis
MONDO:0004247	peptic ulcer disease
MONDO:0004246	lymphatic system disease
MONDO:0004249	pediatric supratentorial ependymoma
MONDO:0004248	pediatric infratentorial ependymoma
MONDO:0004243	vulvar proximal-type epithelioid sarcoma
MONDO:0004242	active peptic ulcer disease
MONDO:0004245	ependymal tumor of brain
MONDO:0004244	proximal-type epithelioid sarcoma
MONDO:0004241	Osgood-Schlatter disease
MONDO:0004240	posterior urethra cancer
MONDO:0016218	Guillain-Barre syndrome
MONDO:0016219	dysmorphism-pectus carinatum-joint laxity syndrome
MONDO:0016214	pulmonary fibrosis-hepatic hyperplasia-bone marrow hypoplasia syndrome
MONDO:0018877	retinitis punctata albescens
MONDO:0018876	mantle cell lymphoma
MONDO:0016215	spastic quadriplegic cerebral palsy
MONDO:0016216	adult hepatocellular carcinoma
MONDO:0018879	lichen planopilaris
MONDO:0016217	mal de Debarquement
MONDO:0018878	branchiootic syndrome
MONDO:0018873	anterior cutaneous nerve entrapment syndrome
MONDO:0016210	alternating hemiplegia
MONDO:0018872	acute megakaryoblastic leukemia
MONDO:0016211	non-papillary transitional cell carcinoma of the bladder
MONDO:0018875	Li-Fraumeni syndrome
MONDO:0016212	cyclosporosis
MONDO:0018874	acute myeloid leukemia
MONDO:0016213	leukonychia totalis-acanthosis-nigricans-like lesions-abnormal hair syndrome
MONDO:0018871	acute myelomonocytic leukemia M4
MONDO:0018870	arterial calcification of infancy
MONDO:0004218	childhood germ cell brain tumor
MONDO:0004217	childhood brain germinoma
MONDO:0006879	optic papillitis
MONDO:0004219	polyvesicular vitelline pattern testicular yolk sac tumor
MONDO:0006877	oophoritis
MONDO:0004214	ovarian endometrioid cystadenofibroma
MONDO:0006878	Moraxellaceae infectious disease
MONDO:0004213	vulvar non-keratinizing squamous cell carcinoma
MONDO:0006875	ocular hypertension
MONDO:0004216	pineal region germinoma
MONDO:0006876	ocular tuberculosis
MONDO:0004215	cutaneous anthrax
MONDO:0043862	voice disorders
MONDO:0004210	colonic L-cell glucagon-like peptide producing tumor
MONDO:0006873	nutritional deficiency disease
MONDO:0006874	obstructive jaundice
MONDO:0006871	non-gestational choriocarcinoma
MONDO:0004212	vulvar keratoacanthoma-like carcinoma
MONDO:0006872	nut allergic reaction
MONDO:0004211	L-cell glucagon-like peptide-producing neuroendocrine tumor
MONDO:0006870	noma
MONDO:0016207	phacoanaphylactic uveitis
MONDO:0016208	solitary rectal ulcer syndrome
MONDO:0018869	cobblestone lissencephaly
MONDO:0016209	benign familial nocturnal alternating hemiplegia of childhood
MONDO:0016203	hypercholesterolemia due to cholesterol 7alpha-hydroxylase deficiency
MONDO:0018866	Aicardi-Goutieres syndrome
MONDO:0016204	idiopathic copper-associated cirrhosis
MONDO:0018865	striate palmoplantar keratoderma
MONDO:0018868	metachromatic leukodystrophy
MONDO:0016205	IRVAN syndrome
MONDO:0016206	idiopathic uveal effusion syndrome
MONDO:0018867	maple syrup urine disease
MONDO:0018862	cat-scratch disease
MONDO:0016200	qualitative or quantitative defects of glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase -
MONDO:0018861	Zellweger-like syndrome without peroxisomal anomalies
MONDO:0018864	Kikuchi-Fujimoto disease
MONDO:0016201	qualitative or quantitative defects of myotilin
MONDO:0016202	autosomal dominant rhegmatogenous retinal detachment
MONDO:0018863	leptospirosis
MONDO:0018860	microlissencephaly-micromelia syndrome
MONDO:0004229	acantholytic variant squamous cell breast carcinoma
MONDO:0004228	hypogonadotropism
MONDO:0006888	paraneoplastic polyneuropathy
MONDO:0004225	monoclonal gammopathy of uncertain significance
MONDO:0006889	paraphimosis
MONDO:0004224	chronic metabolic polyneuropathy
MONDO:0004227	epididymal adenomatoid tumor
MONDO:0006886	thyroid gland papillary and follicular carcinoma
MONDO:0004226	diffuse intraductal papillomatosis
MONDO:0006887	parametritis
MONDO:0004221	uterine corpus perivascular epithelioid cell tumor
MONDO:0006884	panophthalmitis
MONDO:0004220	endometrial endometrioid adenocarcinoma with spindled epithelial cells
MONDO:0004223	polyp of middle ear
MONDO:0043875	tumor lysis syndrome
MONDO:0006882	orchitis
MONDO:0006883	malignant superior sulcus neoplasm
MONDO:0004222	ovarian clear cell cystadenocarcinoma
MONDO:0006880	oral leukoedema
MONDO:0006881	orbital cellulitis
MONDO:0018859	Leigh disease
MONDO:0018858	Graham Little-Piccardi-Lassueur syndrome
MONDO:0018855	keratosis pilaris atrophicans
MONDO:0018854	acquired purpura fulminans
MONDO:0018857	creeping myiasis
MONDO:0018856	lichen amyloidosis
MONDO:0018851	familial keratoacanthoma
MONDO:0018850	proliferating trichilemmal cyst
MONDO:0018853	transgrediens et progrediens palmoplantar keratoderma
MONDO:0018852	achromatopsia
MONDO:0016260	uterine corpus rhabdomyosarcoma
MONDO:0004279	glossopharyngeal motor neuropathy
MONDO:0004276	ceruminoma
MONDO:0004275	osteosarcoma arising in bone Paget disease
MONDO:0004278	infiltrating bladder urothelial carcinoma sarcomatoid variant
MONDO:0004277	gonorrhea
MONDO:0004272	urinary bladder tuberculosis
MONDO:0004271	pregnancy adenoma
MONDO:0004274	mixed epithelial/mesenchymal metaplastic breast carcinoma
MONDO:0004273	breast apocrine adenoma
MONDO:0004270	breast ductal adenoma
MONDO:0016269	high-grade neuroendocrine carcinoma of the corpus uteri
MONDO:0016265	endometrial stromal sarcoma
MONDO:0016266	squamous cell carcinoma of the corpus uteri
MONDO:0016267	undifferentiated carcinoma of the corpus uteri
MONDO:0016268	papillary carcinoma of the corpus uteri
MONDO:0016261	sarcoma of the corpus uteri
MONDO:0016262	leiomyosarcoma of the corpus uteri
MONDO:0016263	primitive neuroectodermal tumor of the corpus uteri
MONDO:0016264	autoimmune hepatitis
MONDO:0004287	pancreatic foamy gland adenocarcinoma
MONDO:0004286	pancreatic intraductal papillary-mucinous neoplasm
MONDO:0004289	glottis verrucous carcinoma
MONDO:0004288	scirrhous breast carcinoma
MONDO:0004283	vulvar clear cell hidradenocarcinoma
MONDO:0004282	eccrine porocarcinoma
MONDO:0004285	pancreatic intraductal papillary-mucinous carcinoma
MONDO:0004284	malignant cystic nephroma
MONDO:0004281	vulvar eccrine porocarcinoma
MONDO:0004280	asymmetric motor neuropathy
MONDO:0016258	uterine corpus carcinofibroma
MONDO:0016259	carcinosarcoma of the corpus uteri
MONDO:0016254	rare variants of adenocarcinoma of the corpus uteri
MONDO:0016255	uterine corpus mixed epithelial and mesenchymal neoplasm
MONDO:0016256	Hennekam syndrome
MONDO:0016257	adenosarcoma of the corpus uteri
MONDO:0016250	rare adenocarcinoma of the breast
MONDO:0016251	salivary gland type cancer of the breast
MONDO:0016252	rare uterine cancer
MONDO:0016253	rare cancer of corpus uteri
MONDO:0028226	autosomal recessive severe congenital neutropenia
MONDO:0004258	female orgasmic disorder
MONDO:0004257	childhood central nervous system mixed germ cell tumor
MONDO:0004259	endocervical carcinoma
MONDO:0004254	focal intraductal papillomatosis
MONDO:0004253	intraductal breast papillomatosis
MONDO:0004256	lumbar spinal canal and spinal cord meningioma
MONDO:0004255	Wolffian adnexal tumor
MONDO:0004250	extrahepatic bile duct papillary adenoma
MONDO:0004252	small intestinal L-cell glucagon-like peptide producing tumor
MONDO:0004251	small intestine neoplasm
MONDO:0016248	familial ovarian cancer
MONDO:0016249	hereditary site-specific ovarian cancer syndrome
MONDO:0016243	hemoglobin E disease
MONDO:0016244	atypical hemolytic-uremic syndrome
MONDO:0016245	ovarian cancer
MONDO:0016246	adenocarcinoma of ovary
MONDO:0016240	hemimelia
MONDO:0016241	alternating hemiplegia of childhood
MONDO:0016242	hemoglobin C disease
MONDO:0004269	breast cystic hypersecretory carcinoma
MONDO:0004268	subareolar duct papillomatosis
MONDO:0004265	acute endometritis
MONDO:0004264	acute gonococcal endometritis
MONDO:0004267	squamous papillomatosis
MONDO:0004266	anal gland adenocarcinoma
MONDO:0004261	periductal breast myoepitheliosis
MONDO:0004260	peptic ulcer perforation
MONDO:0004263	pediatric infratentorial ependymoblastoma
MONDO:0004262	breast myoepitheliosis
MONDO:0016236	kaposiform hemangioendothelioma
MONDO:0018899	posterior cortical atrophy
MONDO:0018898	primary cutaneous lymphoma
MONDO:0016237	diffuse neonatal hemangiomatosis
MONDO:0016238	solitary fibrous tumor
MONDO:0016239	cystinosis
MONDO:0018895	Plummer-Vinson syndrome
MONDO:0016232	rare venous malformation
MONDO:0016233	rare lymphatic system malformation
MONDO:0018894	distal hereditary motor neuropathy
MONDO:0018897	primary cutaneous CD30+ T-cell lymphoproliferative disease
MONDO:0016234	rare arteriovenous malformation
MONDO:0016235	complex vascular malformation with associated anomalies
MONDO:0018896	thrombotic thrombocytopenic purpura
MONDO:0018891	familial tumoral calcinosis
MONDO:0018890	Lyell syndrome
MONDO:0018893	Cobb syndrome
MONDO:0016230	simple vascular malformation
MONDO:0018892	Wyburn-Mason syndrome
MONDO:0016231	capillary malformation
MONDO:0006815	jejunal cancer
MONDO:0006816	arthropathy
MONDO:0006813	intradermal nevus
MONDO:0006814	iritis
MONDO:0006811	intracranial hypotension
MONDO:0006812	intracranial vasospasm
MONDO:0006810	intracranial hypertension
MONDO:0018804	MYO5B-related progressive familial intrahepatic cholestasis
MONDO:0018806	primary intrahepatic lithiasis
MONDO:0018805	bile duct cyst
MONDO:0018800	Kallmann syndrome
MONDO:0018801	congenital bilateral absence of vas deferens
MONDO:0006808	intracranial arterial disease
MONDO:0006809	intracranial embolism
MONDO:0006806	intermediate uveitis
MONDO:0006807	intestinal perforation
MONDO:0006826	kwashiorkor
MONDO:0006827	lateral medullary syndrome
MONDO:0006824	Krebs 2 carcinoma
MONDO:0006825	kuru
MONDO:0006822	Klatskin's tumor
MONDO:0006823	Klinefelter syndrome
MONDO:0006820	kidney cortex necrosis
MONDO:0006821	kidney papillary necrosis
MONDO:0006819	kernicterus
MONDO:0006817	juxtacortical osteosarcoma
MONDO:0006818	keratoconjunctivitis sicca
MONDO:0006804	inflammatory breast carcinoma
MONDO:0006805	intermediate coronary syndrome
MONDO:0006802	inappropriate ADH syndrome
MONDO:0006803	inferior myocardial infarction
MONDO:0006800	ideomotor apraxia
MONDO:0006801	ileal neoplasm
MONDO:0006859	mucinous cystadenoma
MONDO:0006857	middle cerebral artery infarction
MONDO:0006858	mouth disease
MONDO:0006855	mesenteric vascular occlusion
MONDO:0006856	mesothelial neoplasm
MONDO:0006853	mesenchymal chondrosarcoma
MONDO:0006854	mesenchymoma
MONDO:0006851	meconium aspiration syndrome
MONDO:0006852	meningococcal meningitis
MONDO:0006850	maxillary sinus neoplasm
MONDO:0018848	IgG4-related retroperitoneal fibrosis
MONDO:0018847	omphalomesenteric cyst
MONDO:0018849	dentinogenesis imperfecta
MONDO:0018844	urachal cyst
MONDO:0018843	embryonal carcinoma of the central nervous system
MONDO:0018846	penile agenesis
MONDO:0018845	focal myositis
MONDO:0018840	isolated congenital hepatic fibrosis
MONDO:0018842	primary effusion lymphoma
MONDO:0018841	congenital bile acid synthesis defect
MONDO:0004207	pulmonary artery leiomyosarcoma
MONDO:0004206	pulmonary vein leiomyosarcoma
MONDO:0004209	cerebral primitive neuroectodermal tumor
MONDO:0006868	neurogenic bowel
MONDO:0006869	nodular goiter
MONDO:0004208	superior vena cava leiomyosarcoma
MONDO:0006866	neonatal myasthenia gravis
MONDO:0004203	female urethral cancer
MONDO:0004202	adrenal medulla carcinoma
MONDO:0006867	neovascular glaucoma
MONDO:0004205	lymphohistiocytoid mesothelioma
MONDO:0006864	necrotizing sialometaplasia
MONDO:0006865	necrotizing ulcerative gingivitis
MONDO:0004204	squamous cell skin papilloma
MONDO:0006862	myofascial pain syndrome
MONDO:0006863	myxosarcoma
MONDO:0004201	pituitary hypoplasia
MONDO:0006860	mucoepidermoid tumor
MONDO:0006861	myeloid sarcoma
MONDO:0004200	superficial urinary bladder carcinoma
MONDO:0018829	familial schizencephaly
MONDO:0018837	postinfectious vasculitis
MONDO:0018836	subcorneal pustular dermatosis
MONDO:0018839	acquired schizencephaly
MONDO:0018838	lissencephaly spectrum disorders
MONDO:0018833	rare idiopathic macular telangiectasia
MONDO:0018832	HTRA1-related autosomal dominant cerebral small vessel disease
MONDO:0018835	nodular regenerative hyperplasia of the liver
MONDO:0018834	adenylosuccinate synthetase-like 1-related distal myopathy
MONDO:0018831	HTRA1-related cerebral small vessel disease
MONDO:0018830	Kimura disease
MONDO:0006837	low tension glaucoma
MONDO:0006838	lupus vulgaris
MONDO:0006835	lipoid nephrosis
MONDO:0006836	Listeria meningitis
MONDO:0006833	lingual goiter
MONDO:0006834	lip cancer
MONDO:0006831	leukostasis
MONDO:0006832	limited scleroderma
MONDO:0006830	leukoplakia of penis
MONDO:0018819	fibular aplasia-tibial campomelia-oligosyndactyly syndrome
MONDO:0018818	facial diplegia with paresthesias
MONDO:0018826	Lewis-Sumner syndrome
MONDO:0018825	PYCR2-related microcephaly-progressive leukoencephalopathy
MONDO:0018828	pseudo-TORCH syndrome 2
MONDO:0018827	familial chilblain lupus
MONDO:0018822	global developmental delay-visual anomalies-progressive cerebellar atrophy-truncal hypotonia syndrome
MONDO:0018821	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability
MONDO:0018824	pyoderma gangrenosum
MONDO:0018823	X-linked intellectual disability-global development delay-facial dysmorphism-sacral caudal remnant syndrome
MONDO:0018820	recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome
MONDO:0006828	nasal cavity and paranasal sinus lethal midline granuloma
MONDO:0006829	leukemoid reaction
MONDO:0006848	marasmus
MONDO:0006849	mastitis
MONDO:0006846	malignant hypertension
MONDO:0006847	malignant lymphatic vessel tumor
MONDO:0006844	magnesium deficiency
MONDO:0006845	male genital tuberculosis
MONDO:0006842	lymphangiomyoma
MONDO:0006843	macular holes
MONDO:0006840	lymphangiectasis
MONDO:0006841	lymphangioendothelioma
MONDO:0018808	Caroli syndrome
MONDO:0018807	idiopathic ductopenia
MONDO:0018809	idiopathic peliosis hepatis
MONDO:0018815	aneurysmal bone cyst
MONDO:0018814	non-severe combined immunodeficiency
MONDO:0018816	isolated neonatal sclerosing cholangitis
MONDO:0018811	congenital portosystemic shunt
MONDO:0018810	lethal hydranencephaly-diaphragmatic hernia syndrome
MONDO:0018813	high grade B-cell lymphoma with MYC and/ or BCL2 and/or BCL6 rearrangement
MONDO:0018812	MSH3-related attenuated familial adenomatous polyposis
MONDO:0006839	Lutembacher syndrome
MONDO:0041086	mixed anxiety and depressive disorder
MONDO:0041093	central retinal vein occlusion with macular edema
MONDO:0041095	malignant otitis externa caused by Pseudomonas aeruginosa
MONDO:0016060	laryngotracheoesophageal cleft
MONDO:0016061	immunodeficiency with factor H anomaly
MONDO:0016062	median cleft lip/mandibule
MONDO:0004078	mucinous intrahepatic cholangiocarcinoma
MONDO:0004077	lumbosacral lipoma
MONDO:0004079	lung mucous gland adenoma
MONDO:0004074	ovarian mucinous cystadenofibroma
MONDO:0004073	dentin dysplasia
MONDO:0004076	tendon sheath lipoma
MONDO:0043683	Leriche syndrome
MONDO:0004075	infiltrating lipoma
MONDO:0004070	gemistocytic astrocytoma
MONDO:0004072	protoplasmic astrocytoma
MONDO:0004071	childhood cerebral astrocytoma
MONDO:0043678	chromosome inversion
MONDO:0016067	Crandall syndrome
MONDO:0016068	fibrochondrogenesis
MONDO:0016063	Cowden disease
MONDO:0016064	cleft palate
MONDO:0016065	cleft palate-short stature-vertebral anomalies syndrome
MONDO:0016066	sternal cleft
MONDO:0016050	thiamine-responsive encephalopathy
MONDO:0016051	cleft lip-retinopathy syndrome
MONDO:0004089	basaloid carcinoma of the penis
MONDO:0004088	cervical basaloid carcinoma
MONDO:0004085	choroid epithelioid cell melanoma
MONDO:0043693	alcoholic liver diseases
MONDO:0004084	uveal epithelioid cell melanoma
MONDO:0004087	basaloid large cell lung carcinoma
MONDO:0004086	ciliary body epithelioid cell melanoma
MONDO:0004081	extrahepatic bile duct clear cell adenocarcinoma
MONDO:0004080	glottis squamous cell carcinoma
MONDO:0004083	Borst-Jadassohn intraepidermal carcinoma
MONDO:0004082	childhood immature teratoma of ovary
MONDO:0016056	isolated congenital microcephaly
MONDO:0016057	isolated encephalocele
MONDO:0016058	paroxysmal dystonia
MONDO:0016059	cleft lip/palate-deafness-sacral lipoma syndrome
MONDO:0016052	atypical autism
MONDO:0016053	isolated cerebellar vermis hypoplasia
MONDO:0016054	cerebral malformation
MONDO:0016055	syndrome with corpus callosum agenesis /dysgenesis as a major feature
MONDO:0016040	harlequin syndrome
MONDO:0004059	dentin sensitivity
MONDO:0004056	bladder papillary urothelial carcinoma
MONDO:0004055	acute inflammation of lacrimal passage
MONDO:0004058	pancreatic cholera
MONDO:0004057	micropapillary variant infiltrating bladder urothelial carcinoma
MONDO:0004052	rectal cloacogenic carcinoma
MONDO:0004051	aleukemic monocytic leukemia cutis
MONDO:0004054	acute canaliculitis
MONDO:0004053	bartholin gland squamous cell carcinoma
MONDO:0004050	telangiectatic osteogenic sarcoma
MONDO:0016049	congenital myopathy, Paradas type
MONDO:0016045	tetragametic chimerism
MONDO:0016046	familial clubfoot with or without associated lower limb anomalies
MONDO:0016047	endophthalmitis
MONDO:0016048	isolated autosomal dominant hypomagnesemia, Glaudemans type
MONDO:0016041	congenital microgastria
MONDO:0016042	late-onset isolated ACTH deficiency
MONDO:0016043	isolated cleft lip
MONDO:0016044	cleft lip/palate
MONDO:0018691	endometrioid carcinoma of ovary
MONDO:0018690	Holmes-Adie syndrome
MONDO:0004067	gallbladder mucinous adenocarcinoma
MONDO:0004066	intermediate cell type ciliary body melanoma
MONDO:0004069	inborn mitochondrial metabolism disorder
MONDO:0004068	disease of anatomical entity
MONDO:0041052	postherpetic neuralgia
MONDO:0004063	intermediate cell type iris melanoma
MONDO:0004062	intermediate cell type uveal melanoma
MONDO:0004065	intermediate cell type choroid melanoma
MONDO:0004064	iris melanoma
MONDO:0004061	mitochondrial myopathy
MONDO:0004060	peripheral epithelioid sarcoma
MONDO:0016038	calcified aponeurotic fibroma
MONDO:0016039	infantile digital fibromatosis
MONDO:0018697	1p35.2 microdeletion syndrome
MONDO:0016034	cleft lip with or without cleft palate
MONDO:0016035	Nelson syndrome
MONDO:0018696	corticobasal syndrome
MONDO:0016036	Ledderhose disease
MONDO:0018699	pseudohypoparathyroidism with Albright hereditary osteodystrophy
MONDO:0018698	hereditary neuroendocrine tumor of small intestine
MONDO:0016037	superficial Fibromatosis
MONDO:0016030	Evans syndrome
MONDO:0018693	kuru
MONDO:0016031	facial dysmorphism-anorexia-cachexia-eye and skin anomalies syndrome
MONDO:0018692	variably protease-sensitive prionopathy
MONDO:0018695	avian influenza
MONDO:0016032	femoral agenesis/hypoplasia
MONDO:0016033	Cornelia de Lange syndrome
MONDO:0018694	isolated tracheo-esophageal fistula
MONDO:0016092	serous or mucinous cystadenoma of childhood
MONDO:0016093	borderline epithelial tumor of ovary
MONDO:0016094	vaginal germ cell malignant tumor
MONDO:0016095	vaginal rhabdomyosarcoma
MONDO:0016090	late-infantile/juvenile Krabbe disease
MONDO:0016091	adult Krabbe disease
MONDO:0043653	herpes labialis
MONDO:0016096	malignant non-dysgerminomatous germ cell tumor of ovary
MONDO:0016097	symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers
MONDO:0016098	immune-mediated necrotizing myopathy
MONDO:0016099	overlap myositis
MONDO:0016081	coronary arterial fistulas
MONDO:0016082	tracheo-esophageal fistula-hypospadias syndrome
MONDO:0016083	FLOTCH syndrome
MONDO:0016084	Crigler-Najjar syndrome
MONDO:0016080	congenital bronchobiliary fistula
MONDO:0004099	adult cystic teratoma
MONDO:0004096	spinal cord dermoid cyst
MONDO:0004095	B-cell neoplasm
MONDO:0004098	malignant melanocytic peripheral nerve sheath tumor of mediastinum
MONDO:0004097	lipid-rich breast carcinoma
MONDO:0004092	thymic basaloid carcinoma
MONDO:0004091	skin basaloid carcinoma
MONDO:0004094	multiple skull base meningioma
MONDO:0004093	esophageal basaloid carcinoma
MONDO:0004090	vulvar basaloid squamous cell carcinoma
MONDO:0016089	infantile Krabbe disease
MONDO:0016085	Cole-Carpenter syndrome
MONDO:0016086	osteochondritis of tarsal/metatarsal bone
MONDO:0016087	progressive non-infectious anterior vertebral fusion
MONDO:0016088	hypoxanthine-guanine phosphoribosyltransferase deficiency
MONDO:0016070	hereditary gingival fibromatosis
MONDO:0016071	juvenile hyaline fibromatosis
MONDO:0016072	anomaly of puberty or/and menstrual cycle of genetic origin
MONDO:0016073	syndromic microphthalmia
MONDO:0041008	contact dermatitis caused by poison oak
MONDO:0016078	congenital systemic arteriovenous fistula
MONDO:0016079	sporadic Creutzfeldt-Jakob disease
MONDO:0016074	fibrosarcoma
MONDO:0016075	filariasis
MONDO:0016076	lymphatic filariasis
MONDO:0016077	congenital aortopulmonary window
MONDO:0004119	endometrial small cell carcinoma
MONDO:0004118	cystitis cystica
MONDO:0006778	halo nevus
MONDO:0004115	gallbladder small cell carcinoma
MONDO:0004114	urinary bladder small cell neuroendocrine carcinoma
MONDO:0006779	heart aneurysm
MONDO:0004117	ampulla of vater small cell neuroendocrine carcinoma
MONDO:0006776	hairy cell leukemia
MONDO:0004116	esophageal small cell neuroendocrine carcinoma
MONDO:0006777	hairy tongue
MONDO:0004111	refractory hematologic cancer
MONDO:0006774	habitual spontaneous abortion
MONDO:0004110	refractory hairy cell leukemia
MONDO:0006775	haemophilus influenzae meningitis
MONDO:0004113	HCL-v
MONDO:0006772	glycogen storage disease VIII
MONDO:0006773	gonadal tissue neoplasm
MONDO:0004112	radiation cystitis
MONDO:0006770	giant cell reparative granuloma
MONDO:0006771	glossitis
MONDO:0016108	autosomal dominant distal myopathy
MONDO:0016109	autosomal recessive distal myopathy
MONDO:0018767	severe primary trimethylaminuria
MONDO:0016104	infectious disease with peripheral neuropathy
MONDO:0016105	acquired skeletal muscle disease
MONDO:0018766	chronic enteropathy associated with SLCO2A1 gene
MONDO:0018769	isosporiasis
MONDO:0016106	progressive muscular dystrophy
MONDO:0016107	myotonic dystrophy
MONDO:0018768	familial cold autoinflammatory syndrome
MONDO:0016100	rippling muscle disease with myasthenia gravis
MONDO:0018763	Tubulinopathy-associated dysgyria
MONDO:0016101	neurolymphomatosis
MONDO:0018762	non-acquired combined pituitary hormone deficiency
MONDO:0018765	cryptogenic multifocal ulcerous stenosing enteritis
MONDO:0016102	subacute inflammatory demyelinating polyneuropathy
MONDO:0016103	isolated asymptomatic elevation of creatine phosphokinase
MONDO:0018764	microcephalic primordial dwarfism due to RTTN deficiency
MONDO:0018761	SMARCA4-deficient sarcoma of thorax
MONDO:0018760	WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome
MONDO:0004129	cloacogenic carcinoma
MONDO:0004126	thyroiditis
MONDO:0006789	hyperamylasemia
MONDO:0004125	rectum leiomyoma
MONDO:0006787	hidrocystoma
MONDO:0004128	lung occult large cell carcinoma
MONDO:0004127	lung occult adenocarcinoma
MONDO:0006788	hydrophthalmos
MONDO:0004122	thymus small cell carcinoma
MONDO:0006785	Henoch-Schoenlein purpura
MONDO:0006786	hepatic vein thrombosis
MONDO:0004121	prostate small cell carcinoma
MONDO:0004124	prostate stromal sarcoma
MONDO:0006783	hemopneumothorax
MONDO:0043731	lytic metastatic bone lesion
MONDO:0004123	laryngeal small cell carcinoma
MONDO:0006784	hemorrhagic disease of newborn
MONDO:0006781	Helicobacter pylori infectious disease
MONDO:0006782	hemometra
MONDO:0004120	Bartholin gland small cell carcinoma
MONDO:0006780	heartwater disease
MONDO:0043726	multiple organ dysfunction syndrome
MONDO:0018759	childhood-onset progressive contractures-limb-girdle weakness-muscle dystrophy syndrome
MONDO:0043723	Monteggia's fracture
MONDO:0018756	euthyroid Graves orbitopathy
MONDO:0018755	scorpion envenomation
MONDO:0018758	familial patent arterial duct
MONDO:0018757	supratip dysplasia
MONDO:0018752	exercise-induced malignant hyperthermia
MONDO:0018751	genetic otorhinolaryngologic disease
MONDO:0018754	cyanide poisoning
MONDO:0018753	rare disease with malignant hyperthermia
MONDO:0018750	class I glucose-6-phosphate dehydrogenase deficiency
MONDO:0006758	female genital tuberculosis
MONDO:0006759	femoral neuropathy
MONDO:0006756	extracutaneous mastocytoma
MONDO:0006757	extrahepatic cholestasis
MONDO:0006754	esophageal diverticulosis
MONDO:0006755	euthyroid sick syndrome
MONDO:0006752	Erysipelothrix rhusiopathiae infectious disease
MONDO:0006753	Escherichia coli meningitis
MONDO:0006750	Erdheim-Chester disease
MONDO:0006751	Erysipelothrix infectious disease
MONDO:0018749	hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome
MONDO:0018748	linear IgA Dermatosis
MONDO:0018745	superficial pemphigus
MONDO:0018744	oligodendroglial tumor
MONDO:0018747	acquired epidermolysis bullosa
MONDO:0018746	mucous membrane pemphigoid
MONDO:0043735	osteoradionecrosis
MONDO:0018741	paracetamol poisoning
MONDO:0018740	drug-induced methemoglobinemia
MONDO:0018743	immune-mediated acquired neuromuscular junction disease
MONDO:0018742	familial gastric type 1 neuroendocrine tumor
MONDO:0004108	diaphragma sellae meningioma
MONDO:0004107	splenic manifestation of leukemia
MONDO:0006769	gastroparesis
MONDO:0004109	epiglottis neoplasm
MONDO:0006767	gastric antral vascular ectasia
MONDO:0004104	splenic manifestation of hairy cell leukemia
MONDO:0004103	tall cell variant thyroid gland papillary carcinoma
MONDO:0006768	gastric outlet obstruction
MONDO:0006765	Fusobacterium infectious disease
MONDO:0004106	testicular yolk sac tumor, macrocystic pattern
MONDO:0006766	gait apraxia
MONDO:0004105	childhood epithelioid sarcoma
MONDO:0004100	lung mixed small cell and squamous cell carcinoma
MONDO:0006763	frozen shoulder
MONDO:0006764	fungal meningitis
MONDO:0004102	columnar cell variant thyroid gland papillary carcinoma
MONDO:0006761	fibromuscular dysplasia
MONDO:0006762	freemartinism
MONDO:0004101	multicentric papillary thyroid carcinoma
MONDO:0006760	fetal erythroblastosis
MONDO:0018738	benign metanephric tumour
MONDO:0018737	catastrophic antiphospholipid syndrome
MONDO:0018739	neonatal alloimmune neutropenia
MONDO:0018734	verrucous hemangioma
MONDO:0018733	intellectual disability syndrome due to a DYRK1A point mutation
MONDO:0018736	kaposiform lymphangiomatosis
MONDO:0018735	multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome
MONDO:0018730	rare genetic venous malformation
MONDO:0018731	lethal multiple congenital anomalies/dysmorphic syndrome
MONDO:0004159	pancreatic non-invasive mucinous cystadenocarcinoma
MONDO:0004158	pancreatic mucinous-cystic neoplasm with an associated invasive carcinoma
MONDO:0004155	adult central nervous system embryonal carcinoma
MONDO:0004154	central nervous system embryonal carcinoma
MONDO:0004157	pancreatic mucinous cystadenoma
MONDO:0004156	pancreatic mucinous cystadenocarcinoma
MONDO:0004151	spinal meninges cancer
MONDO:0004150	breast giant fibroadenoma
MONDO:0004153	childhood central nervous system embryonal carcinoma
MONDO:0004152	chronic lymphocytic leukemia/small lymphocytic lymphoma with immunoglobulin heavy chain variable-region gene somatic hypermutation
MONDO:0016148	qualitative or quantitative defects of collagen 6
MONDO:0016149	qualitative or quantitative defects of merosin
MONDO:0016144	qualitative or quantitative defects of delta-sarcoglycan
MONDO:0016145	qualitative or quantitative defects of dysferlin
MONDO:0016146	caveolinopathy
MONDO:0016147	qualitative or quantitative defects of dystrophin
MONDO:0016140	sarcoglycanopathy
MONDO:0016141	qualitative or quantitative defects of alpha-sarcoglycan
MONDO:0016142	qualitative or quantitative defects of beta-sarcoglycan
MONDO:0016143	qualitative or quantitative defects of gamma-sarcoglycan
MONDO:0018790	COL4A1 or COL4A2-related cerebral small vessel disease with hemorrhagic tendancy
MONDO:0004169	premenstrual tension
MONDO:0004166	hereditary fallopian tube carcinoma
MONDO:0004165	selective IgD deficiency disease
MONDO:0004168	cribriform variant testicular seminoma
MONDO:0004167	lung clear cell carcinoma
MONDO:0004162	uterine corpus cellular leiomyoma
MONDO:0004161	uterine corpus apoplectic leiomyoma
MONDO:0004164	lymphoepithelioma-like acinar prostate adenocarcinoma
MONDO:0004163	bladder urachal urothelial carcinoma
MONDO:0004160	female stress incontinence
MONDO:0016137	acute and subacute inflammatory demyelinating polyneuropathy
MONDO:0018799	rare hypercholesterolemia
MONDO:0016138	malignant lymphoma with peripheral neuropathy
MONDO:0016139	qualitative or quantitative protein defects in neuromuscular diseases
MONDO:0016133	rare hereditary metabolic disease with peripheral neuropathy
MONDO:0018796	isolated constitutional thrombocytopenia
MONDO:0016134	rare hereditary systemic disease with peripheral neuropathy
MONDO:0018795	syndromic constitutional thrombocytopenia
MONDO:0018798	other genetic dermis disorder
MONDO:0016135	rare hereditary neurologic disease with peripheral neuropathy
MONDO:0018797	genetic cardiac malformation
MONDO:0016136	cerebellar ataxia with peripheral neuropathy
MONDO:0018792	Moyamoya syndrome
MONDO:0016130	fungal myositis
MONDO:0018791	Moyomoya angiopathy
MONDO:0016131	spinal muscular atrophy associated with central nervous system anomaly
MONDO:0018794	cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder
MONDO:0018793	primary condylar hyperplasia
MONDO:0016132	rare hereditary disease with peripheral neuropathy
MONDO:0004136	ovarian endometrioid cystadenoma
MONDO:0006798	hypervitaminosis A
MONDO:0004139	normocytic anemia
MONDO:0006799	hypothalamic neoplasm
MONDO:0004138	maxillary sinus adenoid cystic carcinoma
MONDO:0006796	hypertensive encephalopathy
MONDO:0004133	pituitary gland mixed eosinophil-basophil adenoma
MONDO:0004132	anal canal squamous cell carcinoma
MONDO:0006797	hypertensive retinopathy
MONDO:0006794	hypersensitivity vasculitis
MONDO:0004135	subacute lymphocytic thyroiditis
MONDO:0006795	hypersplenism
MONDO:0004134	benign dermal neurilemmoma
MONDO:0006792	hyperglobulinemic purpura
MONDO:0006793	hyperpituitarism
MONDO:0004131	anal verrucous carcinoma
MONDO:0006790	hypercementosis
MONDO:0004130	anus basaloid carcinoma
MONDO:0006791	hyperemesis gravidarum
MONDO:0016126	viral myositis
MONDO:0018789	COL4A1 or COL4A2-related cerebral small vessel disease with ischemic tendancy
MONDO:0018788	COL4A1 or COL4A2-related cerebral small vessel disease
MONDO:0016127	bacterial myositis
MONDO:0016128	parasitic myositis
MONDO:0016129	eosinophilic gastroenteritis
MONDO:0016122	periodic paralysis
MONDO:0018785	nodular fasciitis
MONDO:0018784	pediatric multiple sclerosis
MONDO:0016123	muscular tumor
MONDO:0018787	genetic cerebral small vessel disease
MONDO:0016124	drug and/or toxic myopathy
MONDO:0018786	pontine autosomal dominant microangiopathy with leukoencephalopathy
MONDO:0016125	infectious, fungal or parasitic myopathy
MONDO:0018781	KID syndrome
MONDO:0018780	congenital generalized hypercontractile muscle stiffness syndrome
MONDO:0016120	myotonic syndrome
MONDO:0018783	fibroblastic rheumatism
MONDO:0016121	congenital myotonia
MONDO:0018782	type 1 interferonopathy
MONDO:0004148	gallbladder papillary neoplasm with an associated invasive carcinoma
MONDO:0004147	noninvasive malignant thymoma
MONDO:0004149	gallbladder pleomorphic giant cell adenocarcinoma
MONDO:0004144	fibrous meningioma
MONDO:0004143	psammomatous meningioma
MONDO:0004146	transitional meningioma
MONDO:0004145	meningothelial meningioma
MONDO:0004140	intermediate malignant teratoma
MONDO:0004142	lung combined large cell neuroendocrine carcinoma
MONDO:0004141	melanomatosis
MONDO:0016119	mitochondrial myopathy
MONDO:0043707	mediastinal disease
MONDO:0016115	bulbospinal muscular atrophy of adulthood
MONDO:0018778	intermediate Charcot-Marie-Tooth disease
MONDO:0016116	generalized bulbospinal muscular atrophy
MONDO:0018777	autosomal dominant preaxial polydactyly-upperback hypertrichosis syndrome
MONDO:0016117	muscular lipidosis
MONDO:0018779	hypercontractile muscle stiffness syndrome
MONDO:0016118	muscular glycogenosis
MONDO:0018774	erythrokeratodermia-cardiomyopathy syndrome
MONDO:0016111	non-dystrophic myopathy with collagen 6 anomaly
MONDO:0018773	autosomal dominant distal axonal motor neuropathy-myofibrillar myopathy syndrome
MONDO:0016112	inclusion myopathy
MONDO:0018776	demyelinating hereditary motor and sensory neuropathy
MONDO:0016113	bulbospinal muscular atrophy
MONDO:0016114	bulbospinal muscular atrophy of childhood
MONDO:0018775	axonal hereditary motor and sensory neuropathy
MONDO:0018770	Jeune syndrome
MONDO:0018772	Joubert syndrome
MONDO:0018771	congenital anomaly of ventricular septum
MONDO:0016110	non-dystrophic myopathy
MONDO:0006705	Bacteroidaceae infectious disease
MONDO:0006706	Bifidobacteriales infectious disease
MONDO:0006703	chronic interstitial cystitis
MONDO:0006704	CNS demyelinating autoimmune disease
MONDO:0006701	chromophobe adenoma
MONDO:0006702	chronic inflammatory demyelinating polyradiculoneuropathy
MONDO:0006700	choroid cancer
MONDO:0006738	eccrine acrospiroma
MONDO:0006739	Ehrlich tumor carcinoma
MONDO:0006736	dysplasia of cervix
MONDO:0006737	dystocia
MONDO:0006734	benign duodenal neoplasm
MONDO:0006735	duodenogastric reflux
MONDO:0006732	drug-induced dyskinesia
MONDO:0006733	dry eye syndrome
MONDO:0006730	drug psychosis
MONDO:0006731	drug-induced akathisia
MONDO:0018719	obsolete rare capillary malformation with associated anomalies
MONDO:0018727	immunodeficiency due to a complement regulatory deficiency
MONDO:0018726	immunodeficiency due to a complement cascade component deficiency
MONDO:0018729	genetic vascular tumor
MONDO:0018728	rare genetic capillary malformation
MONDO:0018723	rare vascular malformation of major vessels
MONDO:0018722	primary lymphedema with associated anomalies
MONDO:0018725	corpus callosum agenesis-macrocephaly-hypertelorism syndrome
MONDO:0018724	X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome
MONDO:0018721	rare combined vascular malformation
MONDO:0018720	common cystic lymphatic malformation
MONDO:0006729	discrete subaortic stenosis
MONDO:0006749	mixed epithelioid and spindle cell melanoma
MONDO:0006747	enterotoxemia
MONDO:0006748	epilepsia partialis continua
MONDO:0006745	endometrioid stromal sarcoma
MONDO:0006746	endomyocardial fibrosis
MONDO:0006743	endocrine tuberculosis
MONDO:0006744	endolymphatic hydrops
MONDO:0006741	encephalomalacia
MONDO:0006742	endemic goiter
MONDO:0006740	empty sella syndrome
MONDO:0018709	X-linked intellectual disability-hypotonia-movement disorder syndrome
MONDO:0018708	squamous cell carcinoma of the oral tongue
MONDO:0018716	partially involuting congenital hemangioma
MONDO:0018715	congenital hemangioma
MONDO:0018718	vascular tumor with associated anomalies
MONDO:0018717	mixed cystic lymphatic malformation
MONDO:0018712	composite hemangioendothelioma
MONDO:0018711	intellectual disability-muscle weakness-short stature-facial dysmorphism syndrome
MONDO:0018714	primary intralymphatic angioendothelioma
MONDO:0018713	retiform hemangioendothelioma
MONDO:0018710	megalencephaly-severe kyphoscoliosis-overgrowth syndrome
MONDO:0006716	coronary thrombosis
MONDO:0006717	cutaneous fibrous histiocytoma
MONDO:0006714	coronary aneurysm
MONDO:0006715	coronary stenosis
MONDO:0006712	corneal edema
MONDO:0006713	corneal neovascularization
MONDO:0006710	complex partial epilepsy
MONDO:0006711	constrictive pericarditis
MONDO:0018705	infantile-onset axonal motor and sensory neuropathy-optic atrophy-neurodegenerative syndrome
MONDO:0018704	actinomycosis
MONDO:0018707	clear cell sarcoma of kidney
MONDO:0018706	syndromic sensorineural deafness due to combined oxidative phosphorylation defect
MONDO:0018701	congenital nemaline myopathy
MONDO:0018700	pseudohypoparathyroidism without Albright hereditary osteodystrophy
MONDO:0018703	isolated splenogonadal fusion
MONDO:0018702	Castleman-Kojima disease
MONDO:0006709	common bile duct neoplasm
MONDO:0006708	Desulfovibrionaceae infectious disease
MONDO:0006727	diastolic heart failure
MONDO:0006728	discitis
MONDO:0006725	diabetic angiopathy
MONDO:0006726	diaphragmatic eventration
MONDO:0006723	denture stomatitis
MONDO:0006724	desmoplastic small round cell tumor
MONDO:0006721	de Quervain disease
MONDO:0006722	dental fluorosis
MONDO:0006720	cystic, mucinous, and serous neoplasm
MONDO:0006718	cutaneous syphilis
MONDO:0006719	cystic lymphangioma
MONDO:0018590	ABeta2M amyloidosis
MONDO:0018592	cutaneous polyarteritis nodosa
MONDO:0018591	ITM2B amyloidosis
MONDO:0043576	endarteritis
MONDO:0018598	neonatal adrenoleukodystrophy
MONDO:0018597	plastic bronchitis
MONDO:0018599	congenital oculomotor nerve palsy
MONDO:0018594	secondary polyarteritis nodosa
MONDO:0018593	primary polyarteritis nodosa
MONDO:0018596	systemic polyarteritis nodosa
MONDO:0018595	single-organ polyarteritis nodosa
MONDO:0018581	progressive encephalomyelitis with rigidity and myoclonus
MONDO:0018580	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome
MONDO:0006598	phototoxic dermatitis
MONDO:0006599	physical urticaria
MONDO:0006596	photoallergic dermatitis
MONDO:0043589	femoral neck fracture
MONDO:0006597	photosensitivity disease
MONDO:0006594	pemphigus
MONDO:0006595	perinatal jaundice due to hepatocellular damage
MONDO:0006592	parapsoriasis
MONDO:0006593	pelvic lipomatosis
MONDO:0006590	palmoplantar keratosis
MONDO:0006591	panniculitis
MONDO:0043579	enteritis
MONDO:0018587	non-recovering obstetric brachial plexus lesion
MONDO:0018586	zinc-responsive necrolytic acral erythema
MONDO:0018589	AApoAIV amyloidosis
MONDO:0018588	ALECT2 amyloidosis
MONDO:0018583	human infection by orthopoxvirus
MONDO:0018582	GCGR-related hyperglucagonemia
MONDO:0018585	pediatric arterial ischemic stroke
MONDO:0018584	placental insufficiency
MONDO:0018570	hypophosphatasia
MONDO:0018579	disorder of ketone body transport
MONDO:0018576	non-progressive predominantly posterior cavitating leukoencephalopathy with peripheral neuropathy
MONDO:0018575	microcephalic primordial dwarfism-insulin resistance syndrome
MONDO:0018578	hypophosphatemic rickets
MONDO:0018577	pseudoxanthoma elasticum-like skin manifestations with retinitis pigmentosa
MONDO:0018572	severe intellectual disability-hypotonia-strabismus-coarse face-planovalgus syndrome
MONDO:0018571	contractures-developmental delay-Pierre Robin syndrome
MONDO:0018574	intellectual disability-expressive aphasia-facial dysmorphism syndrome
MONDO:0018573	intrauterine growth restriction-short stature-early adult-onset diabetes syndrome
MONDO:0043523	cadmium poisoning
MONDO:0043519	burn
MONDO:0043529	carcinoid heart disease
MONDO:0043543	iatrogenic disease
MONDO:0043544	nosocomial infection
MONDO:0043541	viral conjunctivitis
MONDO:0043537	cluster headache syndrome
MONDO:0043555	infantile diarrhea
MONDO:0800001	delayed sleep phase syndrome, susceptibility to
MONDO:0043549	crush syndrome
MONDO:0006659	arteriosclerosis obliterans
MONDO:0006657	apparent mineralocorticoid excess syndrome
MONDO:0006658	arteriolosclerosis
MONDO:0006655	aortic valve prolapse
MONDO:0006656	aortitis
MONDO:0006653	anthracosilicosis
MONDO:0006654	anthracosis
MONDO:0006651	anterior uveitis
MONDO:0006652	anterolateral myocardial infarction
MONDO:0006650	anterior spinal artery syndrome
MONDO:0018649	cerebral visual impairment
MONDO:0018646	sclerosing cholangitis
MONDO:0018645	IgG4-related sclerosing cholangitis
MONDO:0018648	Keratocystic odontogenic tumor
MONDO:0018647	secondary sclerosing cholangitis
MONDO:0018642	NIK deficiency
MONDO:0018641	paroxysmal nocturnal hemoglobinuria
MONDO:0018644	autosomal dominant complex spastic paraplegia type 9B
MONDO:0018643	susceptibility to localized juvenile periodontitis
MONDO:0018640	secondary vasculitis
MONDO:0004009	kidney pelvis sarcomatoid transitional cell carcinoma
MONDO:0004008	flat ductal epithelial atypia
MONDO:0004005	rete ovarii adenoma
MONDO:0006668	bacterial conjunctivitis
MONDO:0004004	motor nerve neuritis
MONDO:0006669	bacterial endocarditis
MONDO:0004007	breast intraductal proliferative lesion
MONDO:0006666	atrophy of thyroid
MONDO:0006667	B- and T-cell mixed leukemia
MONDO:0004006	rete ovarii cystadenofibroma
MONDO:0006664	atrial septal defect
MONDO:0004001	compartment syndrome
MONDO:0006665	chronic atrophic gastritis
MONDO:0004000	childhood pilocytic astrocytoma
MONDO:0006662	aseptic meningitis
MONDO:0004003	pancreatic solid pseudopapillary carcinoma
MONDO:0006663	perinatal asphyxia
MONDO:0004002	pancreatoblastoma
MONDO:0006660	arthus reaction
MONDO:0006661	ascorbic acid deficiency
MONDO:0043606	pathologic fracture
MONDO:0018639	caudal regression-sirenomelia spectrum
MONDO:0018638	pseudohypoaldosteronism
MONDO:0018635	idiopathic phalangeal acro-osteolysis
MONDO:0018634	hereditary amyloidosis
MONDO:0018637	familial chylomicronemia syndrome
MONDO:0018636	autoimmune hemolytic anemia-autoimmune thrombocytopenia-primary immunodeficiency syndrome
MONDO:0018631	Marie Unna hereditary hypotrichosis
MONDO:0018630	hereditary nonpolyposis colon cancer
MONDO:0018633	20q11.2 microdeletion syndrome
MONDO:0018632	11q22.2q22.3 microdeletion syndrome
MONDO:0006639	adrenal cortex carcinoma
MONDO:0006637	acute kidney tubular necrosis
MONDO:0006638	acute retinal necrosis syndrome
MONDO:0006635	Acinetobacter infectious disease
MONDO:0006636	Actinobacillus infectious disease
MONDO:0006633	acalculous cholecystitis
MONDO:0006634	pituitary gland acidophil adenoma
MONDO:0006631	osteoarthritis, toe
MONDO:0006632	osteoarthritis, hand
MONDO:0006630	osteoarthritis, spine
MONDO:0018628	HIV-associated cancer
MONDO:0018627	ACTH-independent Cushing syndrome due to rare cortisol-producing adrenal tumor
MONDO:0018629	focal stiff limb syndrome
MONDO:0018624	spontaneous intracranial hypotension
MONDO:0018623	postpartum psychosis
MONDO:0018626	paratyphoid fever
MONDO:0018625	classic stiff person syndrome
MONDO:0018620	hypothalamic adipsic hypernatraemia syndrome
MONDO:0018622	nut midline carcinoma
MONDO:0018621	lymphoplasmacytic lymphoma without IgM production
MONDO:0006648	anterior compartment syndrome
MONDO:0006649	anterior ischemic optic neuropathy
MONDO:0006646	angioleiomyoma
MONDO:0006647	anterior cerebral artery infarction
MONDO:0006644	alcoholic liver cirrhosis
MONDO:0006645	alcoholic polyneuropathy
MONDO:0006642	alcohol withdrawal delirium
MONDO:0006643	alcoholic cardiomyopathy
MONDO:0006640	adrenal gland hyperfunction
MONDO:0006641	afferent loop syndrome
MONDO:0018609	syndromic hereditary optic neuropathy
MONDO:0018617	baroreflex failure
MONDO:0018616	central serous chorioretinopathy
MONDO:0018619	hyperinsulinemic hypoglycaemia
MONDO:0018618	46,XY disorder of sexual development due to dihydrotestosterone backdoor pathway biosynthesis defect
MONDO:0018613	AH amyloidosis
MONDO:0018612	congenital hypothyroidism
MONDO:0018615	hemicrania continua
MONDO:0018614	undetermined early-onset epileptic encephalopathy
MONDO:0018611	early-onset lamellar cataract
MONDO:0018610	early-onset posterior subcapsular cataract
MONDO:0018680	cutaneous pseudolymphoma
MONDO:0004038	dental enamel hypoplasia
MONDO:0004037	retinal edema
MONDO:0006699	choledocholithiasis
MONDO:0004039	papillary extrahepatic bile duct adenocarcinoma
MONDO:0004034	eye lymphoma
MONDO:0006697	Chlamydophila infectious disease
MONDO:0006698	cholecystolithiasis
MONDO:0004033	familial ovarian carcinoma
MONDO:0006695	cervical rib syndrome
MONDO:0006696	cervix erosion
MONDO:0004035	glomangiomatosis
MONDO:0004030	ureter transitional cell carcinoma
MONDO:0006693	cerebral arterial disease
MONDO:0006694	cerebral atherosclerosis
MONDO:0004032	ovarian seromucinous carcinoma
MONDO:0006691	causalgia
MONDO:0006692	central pontine myelinolysis
MONDO:0004031	ovary mixed epithelial carcinoma
MONDO:0006690	carotid artery thrombosis
MONDO:0016027	benign neonatal seizures
MONDO:0018689	plasma cell leukemia
MONDO:0016028	erythromelalgia
MONDO:0016029	esthesioneuroblastoma
MONDO:0018686	acquired Creutzfeldt-Jakob disease
MONDO:0016023	ocular coloboma
MONDO:0016024	shoulder and thorax deformity-congenital heart disease syndrome
MONDO:0018685	incessant infant ventricular tachycardia
MONDO:0018688	anti-p200 pemphigoid
MONDO:0016025	myoclonic-astastic epilepsy
MONDO:0018687	progressive muscular atrophy
MONDO:0016026	infant epilepsy with migrant focal crisis
MONDO:0018682	congenital insensitivity to pain with severe intellectual disability
MONDO:0018681	neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-hip dysplasia syndrome
MONDO:0016020	frontal encephalocele
MONDO:0018684	idiopathic neonatal atrial flutter
MONDO:0016021	early infantile epileptic encephalopathy
MONDO:0018683	acquired ichthyosis
MONDO:0016022	early myoclonic encephalopathy
MONDO:0004049	combat disorder
MONDO:0004048	immature gastric teratoma
MONDO:0004045	pediatric intraocular retinoblastoma
MONDO:0004044	ureter urothelial papilloma
MONDO:0004047	sphenoidal sinus neoplasm
MONDO:0004046	childhood brain meningioma
MONDO:0004041	urothelial papilloma
MONDO:0004040	urinary bladder inverted papilloma
MONDO:0004043	ureter inverted papilloma
MONDO:0004042	urethra inverted papilloma
MONDO:0018679	primary cutaneous plasmacytosis
MONDO:0016016	toluene embryopathy
MONDO:0018678	polyclonal hyperviscosity syndrome
MONDO:0016017	methimazole embryofetopathy
MONDO:0016018	diabetic embryopathy
MONDO:0016019	Rasmussen subacute encephalitis
MONDO:0016012	diethylstilbestrol syndrome
MONDO:0018675	IgG4-related ophthalmic disease
MONDO:0016013	fetal methylmercury syndrome
MONDO:0018674	IgG4-related submandibular gland disease
MONDO:0018677	visceral heterotaxy
MONDO:0016014	fetal minoxidil syndrome
MONDO:0016015	phenobarbital embryopathy
MONDO:0018676	eosinophilic angiocentric fibrosis
MONDO:0018671	IgG4-related kidney disease
MONDO:0018670	symptomatic form of fragile X syndrome in female carrier
MONDO:0018673	IgG4-related pachymeningitis
MONDO:0016010	vitamin K-antagonist embryofetopathy
MONDO:0016011	fetal alcohol syndrome
MONDO:0018672	IgG4-related aortitis
MONDO:0004019	oxyphilic endometrial endometrioid adenocarcinoma
MONDO:0006679	bladder neck obstruction
MONDO:0004016	pineal region mature teratoma
MONDO:0004015	pineal region teratoma
MONDO:0006677	bile reflux
MONDO:0004018	liver carcinoma
MONDO:0006678	bladder calculus
MONDO:0004017	pineal region immature teratoma
MONDO:0004012	adult botryoid rhabdomyosarcoma
MONDO:0006675	benign monoclonal gammopathy
MONDO:0006676	beriberi
MONDO:0004011	familial melanoma
MONDO:0006673	pituitary gland basophil adenoma
MONDO:0004014	ethmoid sinus ectopic meningioma
MONDO:0006674	benign fibrous mesothelioma
MONDO:0004013	adult vagina botryoid embryonal rhabdomyosarcoma
MONDO:0006671	Bacteroides infectious disease
MONDO:0006672	balanitis
MONDO:0004010	infiltrating renal pelvis/ureter urothelial carcinoma
MONDO:0006670	bacterial meningitis
MONDO:0016009	fetal trimethadione syndrome
MONDO:0018668	scedosporiosis
MONDO:0016005	indomethacin embryofetopathy
MONDO:0016006	Cockayne syndrome
MONDO:0018667	pleural empyema
MONDO:0016007	cocaine embryofetopathy
MONDO:0016008	fetal hydantoin syndrome
MONDO:0018669	snakebite envenomation
MONDO:0018664	ectopia cordis
MONDO:0016001	2-hydroxyglutaric aciduria
MONDO:0018663	regressive spondylometaphyseal dysplasia
MONDO:0016002	Ehlers-Danlos syndrome, kyphoscoliotic type 1
MONDO:0016003	ehrlichiosis
MONDO:0018666	hepatoblastoma
MONDO:0018665	X-linked acrogigantism due to a point mutation
MONDO:0016004	aminopterin/methotrexate embryofetopathy
MONDO:0018660	hemophilia
MONDO:0018662	autosomal recessive brachyolmia
MONDO:0018661	Zika virus infectious disease
MONDO:0016000	familial isolated hypoparathyroidism due to impaired PTH secretion
MONDO:0004027	embryonal cancer
MONDO:0004026	skin tag
MONDO:0006688	byssinosis
MONDO:0004029	ureter small cell carcinoma
MONDO:0004028	small intestinal fibrosarcoma
MONDO:0006689	carcinoid syndrome
MONDO:0006686	brain stem infarction
MONDO:0004023	hepatoblastoma
MONDO:0006687	burning mouth syndrome
MONDO:0004022	parasagittal meningioma
MONDO:0004025	spinal cord embryonal tumor, not otherwise specified
MONDO:0006684	brain edema
MONDO:0006685	brain hypoxia - ischemia
MONDO:0004024	spinal cord neuroblastoma
MONDO:0006682	brachial plexus neuritis
MONDO:0006683	brachial plexus neuropathy
MONDO:0006680	blue nevus
MONDO:0004021	mediastinal malignant lymphoma
MONDO:0004020	mediastinal gray zone lymphoma
MONDO:0006681	Borrelia infectious disease
MONDO:0018657	pigmentation defects-palmoplantar keratoderma-skin carcinoma syndrome
MONDO:0018656	tremor-ataxia-central hypomyelination syndrome
MONDO:0018659	partial duplication of the short arm of chromosome 19
MONDO:0018658	19p13.3 microduplication syndrome
MONDO:0018653	Polymerase proofreading-related adenomatous polyposis
MONDO:0018652	biological anomaly without phenotypic characterization
MONDO:0018655	hypomyelination-cerebellar atrophy-hypoplasia of the corpus callosum syndrome
MONDO:0018654	idiopathic dropped head syndrome
MONDO:0018651	lipoyl transferase 2 deficiency
MONDO:0018650	hemochromatosis type 5
MONDO:0006617	vesiculobullous skin disease
MONDO:0006618	vibratory urticaria
MONDO:0006615	sweat gland disease
MONDO:0006616	toxicodendron dermatitis
MONDO:0006613	stromal corneal pigmentation
MONDO:0006614	subcorneal pustular dermatosis
MONDO:0006611	skin sarcoidosis
MONDO:0006612	steroid lipomatosis
MONDO:0006610	skin atrophy
MONDO:0018606	extensive peripapillary myelinated nerve fibers
MONDO:0018605	disorders of pentose/polyol metabolism
MONDO:0018608	pure autonomic failure
MONDO:0018607	combined hamartoma of the retina and retinal pigment epithelium
MONDO:0018602	necrotizing soft tissue infection
MONDO:0018601	autosomal dominant myopia-midfacial retrusion-sensorineural hearing loss-rhizomelic dysplasia syndrome
MONDO:0018604	familial colorectal cancer type X
MONDO:0018603	interstitial lung disease due to SP-C deficiency
MONDO:0018600	congenital abducens nerve palsy
MONDO:0006608	seborrheic dermatitis
MONDO:0006609	seborrheic infantile dermatitis
MONDO:0006628	Sezary disease
MONDO:0006629	osteoarthritis, hip
MONDO:0006626	diabetic neuropathy
MONDO:0006627	microscopic polyangiitis
MONDO:0006624	overactive bladder
MONDO:0006625	altitude sickness
MONDO:0006622	vulvar seborrheic keratosis
MONDO:0006623	autoimmune pancreatitis type 1
MONDO:0006620	vulva fibroepithelial polyp
MONDO:0006621	vulvar inverted follicular keratosis
MONDO:0006619	viral exanthem
MONDO:0006606	scleredema adultorum
MONDO:0006607	sebaceous gland disease
MONDO:0006604	rosacea
MONDO:0006605	scalp dermatosis
MONDO:0006602	porokeratosis
MONDO:0006603	reactive cutaneous fibrous lesion
MONDO:0006600	pigmentation disease
MONDO:0006601	pityriasis rosea
MONDO:0001642	hordeolum externum
MONDO:0001641	severe pre-eclampsia
MONDO:0001640	gonococcal spondylitis
MONDO:0001646	benign secondary hypertension
MONDO:0001645	crescentic glomerulonephritis
MONDO:0001644	acute proliferative glomerulonephritis
MONDO:0001643	exophthalmic ophthalmoplegia
MONDO:0013628	hyperphosphatasia with intellectual disability syndrome 3
MONDO:0013629	intellectual disability, autosomal recessive 16
MONDO:0013626	psoriasis 14, pustular
MONDO:0013627	3M syndrome 3
MONDO:0013631	lung cancer susceptibility 5
MONDO:0013632	autosomal dominant nonsyndromic deafness 33
MONDO:0013630	Meckel syndrome, type 9
MONDO:0013635	Adams-Oliver syndrome 2
MONDO:0013636	primary biliary cholangitis 4
MONDO:0013633	encephalopathy, acute, infection-induced, susceptibility to, 4
MONDO:0013634	neuropathy, hereditary sensory, type 2C
MONDO:0001639	deficiency anemia
MONDO:0001638	protein-deficiency anemia
MONDO:0001637	cicatricial entropion
MONDO:0001636	mechanical entropion
MONDO:0001653	prepuce cancer
MONDO:0001652	scrotum melanoma
MONDO:0001651	scrotum squamous cell carcinoma
MONDO:0001650	acute cystitis
MONDO:0001657	brain cancer
MONDO:0001656	megaesophagus
MONDO:0001655	dissociated nystagmus
MONDO:0001654	spermatic cord cancer
MONDO:0013617	overgrowth-macrocephaly-facial dysmorphism syndrome
MONDO:0013618	craniofacial anomalies and anterior segment dysgenesis syndrome
MONDO:0013615	craniosynostosis and dental anomalies
MONDO:0013616	pigmented nodular adrenocortical disease, primary, 3
MONDO:0013619	nephrotic syndrome, type 6
MONDO:0013620	congenital myasthenic syndrome 16
MONDO:0013621	LAMB2-related infantile-onset nephrotic syndrome
MONDO:0013624	Rafiq syndrome
MONDO:0013625	Parkinson disease 17
MONDO:0013622	platelet-type bleeding disorder 9
MONDO:0013623	platelet-type bleeding disorder 11
MONDO:0001649	fungal esophagitis
MONDO:0001648	esophageal candidiasis
MONDO:0001647	benign renovascular hypertension
MONDO:0001620	louse-borne relapsing fever
MONDO:0001624	acute sphenoidal sinusitis
MONDO:0001623	cicatricial lagophthalmos
MONDO:0001622	mechanical lagophthalmos
MONDO:0001621	tick-borne relapsing fever
MONDO:0013606	Hermansky-Pudlak syndrome 9
MONDO:0013607	monocytopenia with susceptibility to infections
MONDO:0013604	myopia 21, autosomal dominant
MONDO:0013605	brittle cornea syndrome 2
MONDO:0013608	Joubert syndrome 13
MONDO:0013609	Meckel syndrome, type 10
MONDO:0013610	retinitis pigmentosa 61
MONDO:0013613	Leber congenital amaurosis 16
MONDO:0013614	hypertelorism-preauricular sinus-punctual pits-deafness syndrome
MONDO:0013611	retinitis pigmentosa 62
MONDO:0013612	Geleophysic dysplasia 2
MONDO:0001617	transient global amnesia
MONDO:0001616	lobomycosis
MONDO:0001615	epidemic keratoconjunctivitis
MONDO:0001614	intra-abdominal lymph node mast cell malignancy
MONDO:0001619	relapsing fever
MONDO:0001618	balanoposthitis
MONDO:0001631	vertebral artery insufficiency
MONDO:0001630	branch retinal artery occlusion
MONDO:0001635	bladder squamous papilloma
MONDO:0001634	bladder leiomyoma
MONDO:0001633	central retinal artery occlusion
MONDO:0001632	intracranial arteriosclerosis
MONDO:0013602	paragangliomas 5
MONDO:0013603	myopia 20, autosomal dominant
MONDO:0013600	insomnia
MONDO:0013601	gluthathione peroxidase deficiency
MONDO:0001628	tinea unguium
MONDO:0001627	dementia
MONDO:0001626	traumatic glaucoma
MONDO:0001625	corpus luteum cyst
MONDO:0001629	Jaccoud syndrome
MONDO:0001686	anatomical narrow angle borderline glaucoma
MONDO:0001685	chronic follicular conjunctivitis
MONDO:0001684	exocrine pancreatic insufficiency
MONDO:0001683	pancreatic mucinous ductal ectasia
MONDO:0001689	hypertrophy of tongue papillae
MONDO:0001688	toxic optic neuropathy
MONDO:0001687	diabetic cataract
MONDO:0011009	muscular dystrophy, congenital, with severe central nervous system atrophy and absence of large myelinated fibers
MONDO:0011008	cleft lip/palate-intestinal malrotation-cardiopathy syndrome
MONDO:0001682	diphtheritic peritonitis
MONDO:0001681	diphtheritic cystitis
MONDO:0001680	vaginal mullerian papilloma
MONDO:0013675	multiple mitochondrial dysfunctions syndrome 2
MONDO:0011012	African iron overload
MONDO:0011011	skeletal dysplasia-epilepsy-short stature syndrome
MONDO:0013676	hypermethioninemia due to adenosine kinase deficiency
MONDO:0013673	Wolfram-like syndrome
MONDO:0011014	pleuropulmonary blastoma
MONDO:0011013	autosomal dominant hypocalcemia 1
MONDO:0013674	neurodegeneration with brain iron accumulation 4
MONDO:0013679	sclerosteosis 2
MONDO:0011016	type 1 diabetes mellitus 11
MONDO:0011015	cataract 24
MONDO:0011018	brachyolmia-amelogenesis imperfecta syndrome
MONDO:0013677	Emery-Dreifuss muscular dystrophy 7, autosomal dominant
MONDO:0013678	EDICT syndrome
MONDO:0011017	Naxos disease
MONDO:0013671	hydatidiform mole, recurrent, 2
MONDO:0013672	chromosome 15q25 deletion syndrome
MONDO:0011010	Matthew-Wood syndrome
MONDO:0013670	myopia, high, with cataract and vitreoretinal degeneration
MONDO:0001697	reading disorder
MONDO:0001696	Ehlers-Danlos syndrome
MONDO:0001695	senile ectropion
MONDO:0001694	diffuse interstitial keratitis
MONDO:0001699	tinea manuum
MONDO:0001698	tinea profunda
MONDO:0013659	microcephaly-capillary malformation syndrome
MONDO:0001693	ego-dystonic sexual orientation
MONDO:0001692	pedophilia
MONDO:0001691	laryngeal cartilage cancer
MONDO:0001690	parasitic conjunctivitis
MONDO:0011001	Brugada syndrome 1
MONDO:0013664	46,XY disorder of sex development due to testicular 17,20-desmolase deficiency
MONDO:0013665	epilepsy, juvenile myoclonic, susceptibility to, 9
MONDO:0011000	guanylate cyclase 2E
MONDO:0013662	Barrett esophagus
MONDO:0011003	dilated cardiomyopathy 1E
MONDO:0011002	neuropathy, hereditary motor and sensory, type 6A
MONDO:0013663	platelet-activating factor acetylhydrolase deficiency
MONDO:0013668	tetrasomy 18p
MONDO:0011005	trisomy 18-like syndrome
MONDO:0011004	lissencephaly type 3-metacarpal bone dysplasia syndrome
MONDO:0013669	breast-ovarian cancer, familial, susceptibility to, 4
MONDO:0013666	Stickler syndrome, type 5
MONDO:0011007	diaphragmatic defect-limb deficiency-skull defect syndrome
MONDO:0011006	hereditary spastic paraplegia 9A
MONDO:0013667	myelodysplastic syndrome
MONDO:0013660	arthrogryposis, Perthes disease, and upward gaze palsy
MONDO:0013661	combined malonic and methylmalonic acidemia
MONDO:0001664	submucous uterine fibroid
MONDO:0001663	hole retinal cyst
MONDO:0001662	right bundle branch block
MONDO:0001661	background diabetic retinopathy
MONDO:0001668	internal pathological resorption of tooth
MONDO:0001667	streptobacillus infectious disease
MONDO:0001666	retinal dystrophies primarily involving Bruch's membrane
MONDO:0001665	oculoglandular tularemia
MONDO:0013648	familial progressive hyperpigmentation
MONDO:0013649	hypotrichosis 9
MONDO:0001660	proliferative diabetic retinopathy
MONDO:0013653	Parkinson disease 18, autosomal dominant, susceptibility to
MONDO:0013654	aneurysm, intracranial berry, 11
MONDO:0013651	intellectual disability, autosomal recessive 18
MONDO:0013652	narcolepsy 7
MONDO:0013657	intellectual disability, autosomal dominant 10
MONDO:0013658	intellectual disability, autosomal dominant 11
MONDO:0013655	intellectual disability, autosomal dominant 8
MONDO:0013656	intellectual disability, autosomal dominant 9
MONDO:0001658	nontoxic goiter
MONDO:0013650	hypotrichosis 10
MONDO:0001675	porphyria
MONDO:0001674	diverticulitis of colon
MONDO:0001673	diarrheal disease
MONDO:0025622	Charcot-Marie-Tooth disease, axonal, mitochondrial form, 1
MONDO:0001672	bronchus cancer
MONDO:0001679	crater-like holes of optic disc
MONDO:0001678	intestinal tuberculosis
MONDO:0001677	Rift valley fever
MONDO:0001676	erythropoietic protoporphyria
MONDO:0013639	narcolepsy 6, susceptibility to
MONDO:0013637	primary biliary cholangitis 5
MONDO:0013638	Warburg micro syndrome 3
MONDO:0001671	mucocele of appendix
MONDO:0001670	tooth resorption
MONDO:0013642	holoprosencephaly 11
MONDO:0013643	hyperuricemic nephropathy, familial juvenile type 3
MONDO:0013640	familial retinal arterial macroaneurysm
MONDO:0013641	Warburg micro syndrome 2
MONDO:0013646	chromosome 8q21.11 deletion syndrome
MONDO:0013647	primary microcephaly-epilepsy-permanent neonatal diabetes syndrome
MONDO:0013644	Charcot-Marie-Tooth disease axonal type 2O
MONDO:0013645	autosomal recessive spinocerebellar ataxia 11
MONDO:0001669	lung cancer
MONDO:0001602	labia minora carcinoma
MONDO:0001601	Plasmodium ovale malaria
MONDO:0001600	mucocele of salivary gland
MONDO:0001613	vertebrobasilar insufficiency
MONDO:0001612	carotid stenosis
MONDO:0001611	phlegmonous dacryocystitis
MONDO:0001610	acute dacryocystitis
MONDO:0001606	central nervous system leukemia
MONDO:0001604	lagophthalmos
MONDO:0001603	paralytic lagophthalmos
MONDO:0001609	agranulocytosis
MONDO:0001608	vagus nerve neoplasm
MONDO:0001607	intrapelvic lymph node leukemic reticuloendotheliosis
MONDO:0023093	exertional headache
MONDO:0023094	exogenous ochronosis
MONDO:0023097	exostoses anetodermia brachydactyly type E
MONDO:0023098	extrasystoles short stature hyperpigmentation microcephaly
MONDO:0023099	FRAXD syndrome
MONDO:0023091	esophageal atresia coloboma talipes
MONDO:0023089	erythroplakia
MONDO:0023083	epimetaphyseal dysplasia cataract
MONDO:0023084	epiphyseal dysplasia dysmorphism camptodactyly
MONDO:0023035	Eagle syndrome
MONDO:0025699	Coffin-Siris syndrome 12
MONDO:0023037	elongated styloid process syndrome
MONDO:0023038	eccentrochondrodysplasia
MONDO:0023039	eccrine mucinous carcinoma
MONDO:0025691	dystonia 30
MONDO:0025690	microcephaly, epilepsy, and diabetes syndrome 2
MONDO:0023030	dysmorphism cleft palate loose skin
MONDO:0023031	dysostosis acral with facial and genital abnormalities
MONDO:0011056	Wilms tumor 4
MONDO:0011055	distal monosomy 10p
MONDO:0011058	autosomal dominant nonsyndromic deafness 9
MONDO:0011057	cerebrovascular disorder
MONDO:0011059	holoprosencephaly-craniosynostosis syndrome
MONDO:0011050	microcephaly-cardiac defect-lung malsegmentation syndrome
MONDO:0011052	amelia cleft lip palate hydrocephalus iris coloboma
MONDO:0011051	lethal short-limb skeletal dysplasia, Al Gazali type
MONDO:0011054	autosomal recessive amelia
MONDO:0011053	intellectual disability-sparse hair-brachydactyly syndrome
MONDO:0023023	neonatal dacryocystitis
MONDO:0023020	dwarfism deafness retinitis pigmentosa
MONDO:0023021	dwarfism lethal type advanced bone age
MONDO:0023022	dwarfism thin bones multiple fractures
MONDO:0011045	MMEP syndrome
MONDO:0011044	ectrodactyly of lower limbs, congenital heart defect, and micrognathia
MONDO:0011047	deafness-epiphyseal dysplasia-short stature syndrome
MONDO:0011046	short stature, Brussels type
MONDO:0011049	fine-Lubinsky syndrome
MONDO:0011048	epilepsy-microcephaly-skeletal dysplasia syndrome
MONDO:0011041	ectodermal dysplasia with natal teeth, Turnpenny type
MONDO:0011040	spinal dysplasia, Anhalt type
MONDO:0011043	myelodysplasia, immunodeficiency, facial dysmorphism, short stature, and psychomotor delay
MONDO:0011042	Martinez-Frias syndrome
MONDO:0023013	Duker-Weiss-Siber syndrome
MONDO:0023015	duodenal atresia tetralogy of fallot
MONDO:0023016	duplication of leg mirror foot
MONDO:0023017	duplication of the thumb unilateral biphalangeal
MONDO:0023018	dupont sellier chochillon syndrome
MONDO:0023019	dwarfism bluish sclerae
MONDO:0023011	Wilson-Mikity syndrome
MONDO:0011034	odontomicronychial dysplasia
MONDO:0013697	intellectual disability, autosomal recessive 29
MONDO:0013698	arthrogryposis, distal, type 1B
MONDO:0011033	type 1 diabetes mellitus 13
MONDO:0011036	porencephaly-cerebellar hypoplasia-internal malformations syndrome
MONDO:0013695	colorectal cancer, hereditary nonpolyposis, type 6
MONDO:0011035	neurofibromatosis-Noonan syndrome
MONDO:0013696	chromosome 2P16.3 deletion syndrome
MONDO:0011038	cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome
MONDO:0011037	renal dysplasia, cystic, susceptibility to
MONDO:0013699	colorectal cancer, hereditary nonpolyposis, type 4
MONDO:0011039	atrophia maculosa varioliformis cutis, familial
MONDO:0013690	Pitt-Hopkins-like syndrome 2
MONDO:0013693	inflammatory skin and bowel disease, neonatal, 1
MONDO:0011030	epithelial basolateral chloride conductance regulator, rabbit, homolog of
MONDO:0013694	intellectual disability, autosomal recessive 31
MONDO:0011032	autosomal dominant nonsyndromic deafness 11
MONDO:0013691	Feingold syndrome type 2
MONDO:0011031	autosomal dominant nonsyndromic deafness 10
MONDO:0013692	BAP1-related tumor predisposition syndrome
MONDO:0023002	double discordia
MONDO:0023003	double fingernail of fifth finger
MONDO:0023005	double uterus-hemivagina-renal agenesis
MONDO:0025667	limbal stem cell deficiency
MONDO:0023006	doxorubicin induced cardiomyopathy
MONDO:0023007	Drachtman Weinblatt Sitarz syndrome
MONDO:0023008	drachtman weinblatt sitarz syndrome
MONDO:0011019	alopecia-intellectual disability-hypergonadotropic hypogonadism syndrome
MONDO:0023000	dobrow syndrome
MONDO:0013686	distal myopathy, Tateyama type
MONDO:0011023	hereditary mixed polyposis syndrome
MONDO:0011022	Potocki-Shaffer syndrome
MONDO:0013687	autosomal recessive spinocerebellar ataxia 12
MONDO:0013684	vesicoureteral reflux 6
MONDO:0011025	Cayman type cerebellar ataxia
MONDO:0013685	pancreatic cancer, susceptibility to, 4
MONDO:0011024	dermatitis herpetiformis, familial
MONDO:0011027	diabetes mellitus, noninsulin-dependent, 1
MONDO:0011026	autosomal recessive congenital ichthyosis 4A
MONDO:0013688	linear and whorled nevoid hypermelanosis
MONDO:0011029	myeloid tumor suppressor
MONDO:0013689	ovarian dysgenesis 3
MONDO:0011028	autosomal recessive limb-girdle muscular dystrophy type 2F
MONDO:0013682	vesicoureteral reflux 4
MONDO:0013683	vesicoureteral reflux 5
MONDO:0011021	neuronal intestinal dysplasia, type B
MONDO:0013680	cognitive impairment with or without cerebellar ataxia
MONDO:0013681	alpha-methylacyl-CoA racemase deficiency
MONDO:0011020	osteoporosis-oculocutaneous hypopigmentation syndrome
MONDO:0023079	epidermal nevus vitamin D resistant rickets
MONDO:0011090	isolated hereditary congenital facial paralysis
MONDO:0023071	enterovirus antenatal infection
MONDO:0023072	envenomization by Bothrops lanceolatus
MONDO:0023073	eosinophilic cryptitis
MONDO:0023076	eosinophilic pustular folliculitis
MONDO:0011099	human HOXA1 syndromes
MONDO:0011092	ribbing disease
MONDO:0011091	Charcot-Marie-Tooth disease type 2D
MONDO:0011094	dilated cardiomyopathy 1C
MONDO:0011093	mucopolysaccharidosis type 9
MONDO:0011096	autosomal agammaglobulinemia
MONDO:0011095	dilated cardiomyopathy 1D
MONDO:0011098	prostate cancer, hereditary, 1
MONDO:0011097	Axenfeld-Rieger syndrome type 2
MONDO:0023067	endemic Kaposi sarcoma
MONDO:0023068	engelhard yatziv syndrome
MONDO:0023069	enlarged vestibular aqueduct syndrome
MONDO:0023061	enamel hypoplasia cataract hydrocephaly
MONDO:0023062	encephalocele anencephaly
MONDO:0023065	encephalopathy recurrent of childhood
MONDO:0023066	enchondromatosis dwarfism deafness
MONDO:0011089	patent ductus venosus
MONDO:0011088	congenital myasthenic syndrome 1A
MONDO:0011081	dislocation of the hip-dysmorphism syndrome
MONDO:0011080	progressive deafness with stapes fixation
MONDO:0011083	trichodental syndrome
MONDO:0011082	oculoauriculofrontonasal syndrome
MONDO:0011085	Charcot-Marie-Tooth disease type 4D
MONDO:0011084	psoriasis 3, susceptibility to
MONDO:0011087	inflammatory bowel disease 2
MONDO:0011086	severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-positive
MONDO:0023059	Elliott ludman Teebi syndrome
MONDO:0023050	ectrodactyly cardiopathy dysmorphism
MONDO:0023052	ectrodactyly polydactyly
MONDO:0023054	klumpke's paralysis
MONDO:0011078	anterior chamber cleavage disorder, cerebellar hypoplasia, hypothyroidism, and tracheal stenosis
MONDO:0011077	microcephaly, corpus callosum dysgenesis, and cleft lip/palate
MONDO:0011079	rhizomelic dysplasia, Patterson-Lowry type
MONDO:0011070	van Maldergem syndrome 1
MONDO:0035009	isolated mesenteric vein thrombosis
MONDO:0035008	isolated splenic vein thrombosis
MONDO:0011072	diabetes mellitus, noninsulin-dependent, 2
MONDO:0011071	hereditary thrombocytopenia and hematologic cancer predisposition syndrome
MONDO:0011074	autosomal dominant nonsyndromic deafness 7
MONDO:0011073	diabetes mellitus, transient neonatal, 1
MONDO:0035004	serine biosynthesis pathway deficiency, infantile/juvenile form
MONDO:0011076	myofibrillar myopathy 1
MONDO:0011075	retinitis pigmentosa 18
MONDO:0023045	ectodermal dysplasia arthrogryposis diabetes mellitus
MONDO:0023046	ectodermal dysplasia blindness
MONDO:0023048	ectodermal dysplasia neurosensory deafness
MONDO:0023040	ectodermal dysplasia Bartalos type
MONDO:0023041	ectodermal dysplasia Berlin type
MONDO:0023042	ectodermal dysplasia margarita type
MONDO:0023043	ectodermal dysplasia alopecia preaxial polydactyly
MONDO:0011067	autosomal recessive nonsyndromic deafness 12
MONDO:0011066	Charcot-Marie-Tooth disease type 4B1
MONDO:0011069	cervical ribs, Sprengel anomaly, anal atresia, and urethral obstruction
MONDO:0011068	type 1 diabetes mellitus 12
MONDO:0011061	chorea, remitting, with nystagmus and cataract
MONDO:0011060	early-onset non-syndromic cataract
MONDO:0011063	hidrotic ectodermal dysplasia, Christianson-Fourie type
MONDO:0011062	aprosencephaly cerebellar dysgenesis
MONDO:0011065	Hunter-McAlpine craniosynostosis
MONDO:0011064	lethal chondrodysplasia, Seller type
MONDO:0001521	intermittent explosive disorder
MONDO:0001520	kleptomania
MONDO:0001525	thyrocalcitonin secretion disease
MONDO:0001524	globe disease
MONDO:0001523	luxation of globe
MONDO:0001522	pyromania
MONDO:0013507	granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 3
MONDO:0013508	myopia 19, autosomal dominant
MONDO:0013505	spermatogenic failure 9
MONDO:0013506	schizophrenia 16
MONDO:0013509	intellectual disability, autosomal dominant 6
MONDO:0013510	melanoma, cutaneous malignant, susceptibility to, 6
MONDO:0013511	cyanosis, transient neonatal
MONDO:0013514	hypotrichosis 3
MONDO:0013515	osteogenesis imperfecta type 6
MONDO:0013512	hemoglobin H disease
MONDO:0013513	atrial fibrillation, familial, 9
MONDO:0001518	spastic entropion
MONDO:0001517	dysentery
MONDO:0001516	spinal muscular atrophy
MONDO:0001515	corneal degeneration
MONDO:0001519	entropion
MONDO:0001532	capillariasis
MONDO:0001531	blood coagulation disease
MONDO:0001530	secondary hyperparathyroidism of renal origin
MONDO:0001536	vaginal leiomyoma
MONDO:0001535	vagus nerve disease
MONDO:0001534	ocular hyperemia
MONDO:0001533	pes anserinus tendinitis or bursitis
MONDO:0013500	immunodeficiency 51
MONDO:0013503	candidiasis, familial, 6
MONDO:0013504	spermatogenic failure 8
MONDO:0013501	frontotemporal dementia and/or amyotrophic lateral sclerosis 6
MONDO:0013502	amyloidosis, primary localized cutaneous, 2
MONDO:0001529	pancytopenia
MONDO:0001528	vulva cancer
MONDO:0001527	conjugate gaze palsy
MONDO:0001526	labia minora cancer
MONDO:0001503	primary eye hypotony
MONDO:0001502	retroperitoneum carcinoma
MONDO:0001501	retroperitoneal sarcoma
MONDO:0001500	gender identity disorder
MONDO:0001510	lateral displacement of eye
MONDO:0001514	prolapse of urethra
MONDO:0001513	pulsating exophthalmos
MONDO:0001512	intermittent proptosis
MONDO:0001511	thyrotoxic exophthalmos
MONDO:0001507	viral labyrinthitis
MONDO:0001506	prostatocystitis
MONDO:0001505	alcoholic hepatitis
MONDO:0001504	fetishism
MONDO:0001509	endocrine exophthalmos
MONDO:0001508	patulous eustachian tube
MONDO:0001565	abnormal retinal correspondence
MONDO:0001564	binocular vision disease
MONDO:0001563	vestibulocochlear nerve disease
MONDO:0001562	displacement of cardia through esophageal hiatus
MONDO:0001569	acoustic neuroma
MONDO:0001568	mixed receptive-expressive language disorder
MONDO:0001567	nephrocalcinosis
MONDO:0001566	hypercalcemia disease
MONDO:0013549	N-acetylaspartate deficiency
MONDO:0001561	pyloric stenosis
MONDO:0001560	hypertrophic pyloric stenosis
MONDO:0013554	psoriasis 13, susceptibility to
MONDO:0013555	Hermansky-Pudlak syndrome 3
MONDO:0013552	hereditary spastic paraplegia 52
MONDO:0013553	immunodeficiency-centromeric instability-facial anomalies syndrome 2
MONDO:0013558	Hermansky-Pudlak syndrome 6
MONDO:0013559	Hermansky-Pudlak syndrome 7
MONDO:0013556	Hermansky-Pudlak syndrome 4
MONDO:0013557	Hermansky-Pudlak syndrome 5
MONDO:0001559	perineocele
MONDO:0013550	distal myopathy with posterior leg and anterior hand involvement
MONDO:0013551	hereditary spastic paraplegia 47
MONDO:0001576	telangiectasis
MONDO:0001575	chronic gonococcal salpingitis
MONDO:0001574	capillary disease
MONDO:0001573	Friedreich ataxia
MONDO:0001579	corneal staphyloma
MONDO:0001578	hernia of ovary and fallopian tube
MONDO:0001577	respiratory syncytial virus infectious disease
MONDO:0013538	alpha-2-macroglobulin deficiency
MONDO:0013539	hypotonia-failure to thrive-microcephaly syndrome
MONDO:0001572	leiomyoma
MONDO:0001571	gynecomastia
MONDO:0001570	locked-in syndrome
MONDO:0013543	trypsinogen deficiency
MONDO:0013544	atrial fibrillation, familial, 11
MONDO:0013541	complex cortical dysplasia with other brain malformations 1
MONDO:0013542	Moyamoya disease 5
MONDO:0013547	mitochondrial complex V (ATP synthase) deficiency nuclear type 3
MONDO:0013548	acetyl-CoA acetyltransferase-2 deficiency
MONDO:0013545	atrial fibrillation, familial, 12
MONDO:0013546	mitochondrial complex V (ATP synthase) deficiency nuclear type 2
MONDO:0025518	aspirin allergy
MONDO:0025517	shrimp allergy
MONDO:0013540	deafness-lymphedema-leukemia syndrome
MONDO:0025510	pythiosis
MONDO:0001543	lesion of sciatic nerve
MONDO:0001542	common peroneal nerve lesion
MONDO:0001541	plantar nerve lesion
MONDO:0025512	type II hypersensitivity reaction disease
MONDO:0025511	inherited neuroendocrine tumor
MONDO:0001540	bagassosis
MONDO:0025514	livedoid vasculopathy
MONDO:0001547	atrophic nonflaccid tympanic membrane
MONDO:0001546	hypermobility of coccyx
MONDO:0025513	autoimmune urticaria
MONDO:0001545	von willebrand disease
MONDO:0001544	tibial nerve palsy
MONDO:0013529	catecholaminergic polymorphic ventricular tachycardia 3
MONDO:0013527	lissencephaly 4
MONDO:0013528	intellectual disability, autosomal recessive 14
MONDO:0013532	protein Z deficiency
MONDO:0013533	hyperlipidemia due to hepatic triglyceride lipase deficiency
MONDO:0013530	atrial fibrillation, familial, 10
MONDO:0013531	PSPH deficiency
MONDO:0013536	heme oxygenase 1 deficiency
MONDO:0013537	autosomal recessive nonsyndromic deafness 29
MONDO:0013534	apolipoprotein c-III deficiency
MONDO:0013535	hydroxyacyl glutathione hydrolase deficiency
MONDO:0025506	porcine postweaning multisystemic wasting syndrome
MONDO:0001539	retinal perforation
MONDO:0001538	retinal ischemia
MONDO:0001537	tuberculous epididymitis
MONDO:0001554	phacogenic glaucoma
MONDO:0001553	phacolytic glaucoma
MONDO:0001552	dyscalculia
MONDO:0001551	ulceration of vulva
MONDO:0001558	Potter sequence
MONDO:0001557	olecranon bursitis
MONDO:0001556	urethral obstruction
MONDO:0025505	mink viral enteritis
MONDO:0001555	neonatal thyrotoxicosis
MONDO:0013518	pituitary hormone deficiency, combined, 6
MONDO:0013519	dyskeratosis congenita, autosomal recessive 2
MONDO:0013516	retinitis pigmentosa 60
MONDO:0013517	beta-thalassemia HBB/LCRB
MONDO:0001550	Duane retraction syndrome
MONDO:0013521	dyskeratosis congenita, autosomal dominant 2
MONDO:0013522	dyskeratosis congenita, autosomal dominant 3
MONDO:0013520	dyskeratosis congenita, autosomal recessive 3
MONDO:0013525	primary ciliary dyskinesia 16
MONDO:0013526	progressive myoclonic epilepsy type 6
MONDO:0013523	Nestor-Guillermo progeria syndrome
MONDO:0013524	bleeding diathesis due to thromboxane synthesis deficiency
MONDO:0001549	hemolytic-uremic syndrome
MONDO:0001548	hepatic coma
MONDO:0013598	myostatin-related muscle hypertrophy
MONDO:0013599	autoimmune enteropathy and endocrinopathy - susceptibility to chronic infections syndrome
MONDO:0013596	nonsyndromic congenital nail disorder 10
MONDO:0013597	platelet-type bleeding disorder 14
MONDO:0013590	Stickler syndrome, type 4
MONDO:0013591	epiphyseal dysplasia, multiple, 6
MONDO:0013594	spinocerebellar ataxia type 36
MONDO:0013595	hyperbiliverdinemia
MONDO:0013592	nonsyndromic congenital nail disorder 9
MONDO:0013593	autosomal dominant nonsyndromic deafness 64
MONDO:0013587	glycogen storage disease due to lactate dehydrogenase H-subunit deficiency
MONDO:0013588	Perrault syndrome 3
MONDO:0013585	hydrolethalus syndrome 2
MONDO:0013586	Chitotriosidase deficiency
MONDO:0013589	focal segmental glomerulosclerosis 6
MONDO:0013580	pyruvate dehydrogenase E1-beta deficiency
MONDO:0013583	occipital pachygyria and polymicrogyria
MONDO:0013584	hereditary sensory neuropathy-deafness-dementia syndrome
MONDO:0013581	intellectual disability, autosomal dominant 2
MONDO:0013582	mosaic variegated aneuploidy syndrome 2
MONDO:0001587	mucopolysaccharidosis type 4
MONDO:0001586	mucopolysaccharidosis type 1
MONDO:0001585	hallucinogen abuse
MONDO:0025556	isocyanate induced asthma
MONDO:0001584	ocular motility disease
MONDO:0001589	vaginal enterocele
MONDO:0001588	chronic lacrimal gland enlargement
MONDO:0001583	diabetic polyneuropathy
MONDO:0001582	cicatricial ectropion
MONDO:0001581	tolosa-hunt syndrome
MONDO:0001580	lacrimal duct cancer
MONDO:0013576	recurrent infections associated with rare immunoglobulin isotypes deficiency
MONDO:0013577	Lipedema
MONDO:0013574	cutis laxa - Marfanoid syndrome
MONDO:0013575	plasma fibronectin deficiency
MONDO:0013578	DYRK1A-related intellectual disability syndrome
MONDO:0013579	methylmalonate semialdehyde dehydrogenase deficiency
MONDO:0013572	Keppen-Lubinsky syndrome
MONDO:0013573	cranioectodermal dysplasia 3
MONDO:0013570	combined oxidative phosphorylation defect type 8
MONDO:0013571	acatalasia
MONDO:0001598	benign lymphoepithelial lesion of salivary gland
MONDO:0001597	submandibular gland disease
MONDO:0001596	hypochondriasis
MONDO:0001595	choreatic disease
MONDO:0001599	Mikulicz disease
MONDO:0001590	quadriplegia
MONDO:0001594	Achilles bursitis
MONDO:0001593	rectal disease
MONDO:0001592	prolapse of female genital organ
MONDO:0001591	senile entropion
MONDO:0013565	Fanconi anemia complementation group G
MONDO:0013566	Fanconi anemia complementation group L
MONDO:0013563	multiple congenital anomalies-hypotonia-seizures syndrome 1
MONDO:0013564	anhaptoglobinemia
MONDO:0013569	short-rib thoracic dysplasia 7 with or without polydactyly
MONDO:0013567	atrial septal defect 3
MONDO:0013568	sick sinus syndrome 3, susceptibility to
MONDO:0013561	chondrodysplasia with joint dislocations, gPAPP type
MONDO:0013562	aspergillosis, susceptibility to
MONDO:0013560	Hermansky-Pudlak syndrome 8
MONDO:0025598	pneumonia caused by chlamydia
MONDO:0001400	schwannoma of ureter
MONDO:0001404	ecthyma
MONDO:0001403	labium majus cancer
MONDO:0001402	vaginal cancer
MONDO:0001401	female breast nipple and areola cancer
MONDO:0001411	synostosis
MONDO:0001410	postmenopausal atrophic vaginitis
MONDO:0001415	atrophy of testis
MONDO:0001414	osteopoikilosis
MONDO:0001413	ulceroglandular tularemia
MONDO:0001412	conjunctival concretion
MONDO:0001408	ischemic neuropathy
MONDO:0001407	tracheal cancer
MONDO:0001406	peripheral nervous system neoplasm
MONDO:0001405	dermatophytosis of groin and perianal area
MONDO:0001409	esophagitis
MONDO:0001444	Chagas disease
MONDO:0001443	tympanosclerosis
MONDO:0001442	dysthymic disorder
MONDO:0025412	feline panleukopenia
MONDO:0001441	pica disease
MONDO:0001448	alveolar echinococcosis
MONDO:0001447	detrusor sphincter dyssynergia
MONDO:0025417	fowlpox
MONDO:0001446	low compliance bladder
MONDO:0001445	neurogenic bladder
MONDO:0013428	Meier-Gorlin syndrome 2
MONDO:0013429	retinitis pigmentosa 40
MONDO:0001440	neurotrophic keratoconjunctivitis
MONDO:0013433	primary sclerosing cholangitis
MONDO:0013434	primary ciliary dyskinesia 14
MONDO:0013431	Meier-Gorlin syndrome 4
MONDO:0013432	Meier-Gorlin syndrome 5
MONDO:0013437	retinitis pigmentosa 43
MONDO:0013438	pontocerebellar hypoplasia type 2D
MONDO:0013435	primary ciliary dyskinesia 15
MONDO:0013436	retinitis pigmentosa 39
MONDO:0001439	episcleritis periodica fugax
MONDO:0001438	postinflammatory pulmonary fibrosis
MONDO:0013430	Meier-Gorlin syndrome 3
MONDO:0001455	retinal lattice degeneration
MONDO:0001454	Blessig's cysts
MONDO:0001453	senile reticular retinal degeneration
MONDO:0001452	pseudoretinitis pigmentosa
MONDO:0025404	coronaviral enteritis of turkeys
MONDO:0001459	radial neuropathy
MONDO:0001458	ulnar nerve lesion
MONDO:0001457	secondary vitreoretinal degeneration
MONDO:0001456	cobblestone retinal degeneration
MONDO:0013419	complement component C1s deficiency
MONDO:0013417	complement component 3 deficiency
MONDO:0013418	aortic aneurysm, familial thoracic 7
MONDO:0001451	peripheral retinal degeneration
MONDO:0001450	arachnoiditis
MONDO:0013422	type I complement component 8 deficiency
MONDO:0013423	immunodeficiency due to MASP-2 deficiency
MONDO:0013420	age related macular degeneration 12
MONDO:0013421	type II complement component 8 deficiency
MONDO:0013426	aneurysm-osteoarthritis syndrome
MONDO:0013427	immunodeficiency 31B
MONDO:0013424	3p- syndrome
MONDO:0013425	retinitis pigmentosa 20
MONDO:0001449	lymphocytic choriomeningitis
MONDO:0001422	primary aldosteronism
MONDO:0001421	frontal lobe neoplasm
MONDO:0001420	trigeminal nerve neoplasm
MONDO:0001426	mediastinum neurofibroma
MONDO:0001425	Rett syndrome
MONDO:0001424	sarcoid meningitis
MONDO:0001423	drug-induced mental disorder
MONDO:0013408	FADD-related immunodeficiency
MONDO:0013409	age related macular degeneration 5
MONDO:0013406	age related macular degeneration 6
MONDO:0013407	retinitis pigmentosa 47
MONDO:0013411	cataract 16 multiple types
MONDO:0013412	hypertrophic cardiomyopathy 9
MONDO:0013410	46,XY sex reversal 6
MONDO:0013415	chromosome 17p13.1 deletion syndrome
MONDO:0013416	age related macular degeneration 8
MONDO:0013413	retinitis pigmentosa 45
MONDO:0013414	retinitis pigmentosa 44
MONDO:0001419	trachea squamous cell carcinoma
MONDO:0001418	trachea sarcoma
MONDO:0001417	tracheal lymphoma
MONDO:0001416	female reproductive organ cancer
MONDO:0001433	vaginal disease
MONDO:0001432	sodoku disease
MONDO:0001431	toxic or nutritional optic neuropathy
MONDO:0001430	deep corneal vascularisation
MONDO:0001437	pulmonary alveolar proteinosis
MONDO:0001436	hemosiderosis
MONDO:0001435	bullous retinoschisis
MONDO:0001434	inflammatory spondylopathy
MONDO:0013400	Congenital adrenal insuffiency with 46, XY sex reversal OR 46,XY disorder of sex development-adrenal insufficiency due to CYP11A1 deficiency
MONDO:0013401	hereditary spastic paraplegia 51
MONDO:0013404	hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase
MONDO:0013405	retinitis pigmentosa 49
MONDO:0013402	retinitis pigmentosa 27
MONDO:0013403	heterotaxy, visceral, 4, autosomal
MONDO:0001429	transient arthropathy
MONDO:0001428	pylorospasm
MONDO:0001427	Dieulafoy lesion
MONDO:0001488	anterior corneal pigmentation
MONDO:0001487	intrahepatic bile duct cancer
MONDO:0025457	pulmonary adenomatosis, ovine
MONDO:0001486	Vogt-Koyanagi-Harada disease
MONDO:0001485	atypical depressive disorder
MONDO:0025459	rinderpest
MONDO:0001489	urticaria pigmentosa
MONDO:0001480	malignant tumor of undescended testis
MONDO:0001484	paranoid schizophrenia
MONDO:0001483	Crimean-Congo hemorrhagic fever
MONDO:0025453	pneumonia, progressive interstitial, of sheep
MONDO:0001482	testicular leukemia
MONDO:0001481	femoral vein thrombophlebitis
MONDO:0013477	hypertrophic cardiomyopathy 20
MONDO:0013478	PLIN1-related familial partial lipodystrophy
MONDO:0013475	hypertrophic cardiomyopathy 18
MONDO:0013476	hypertrophic cardiomyopathy 19
MONDO:0013479	dilated cardiomyopathy 1HH
MONDO:0013470	generalized epilepsy with febrile seizures plus, type 7
MONDO:0013473	Hirschsprung disease, cardiac defects, and autonomic dysfunction
MONDO:0013474	hypertrophic cardiomyopathy 17
MONDO:0013471	autosomal recessive nonsyndromic deafness 61
MONDO:0013472	fatal infantile hypertonic myofibrillar myopathy
MONDO:0001499	retroperitoneal lymphoma
MONDO:0001498	varicocele
MONDO:0001497	male genital organ vascular disease
MONDO:0001496	male genital organ stricture
MONDO:0025445	Wieacker-Wolff syndrome (spectrum)
MONDO:0025449	paratuberculosis
MONDO:0001491	cough variant asthma
MONDO:0001490	corneal granular dystrophy
MONDO:0001495	hematocele of tunica vaginalis testis
MONDO:0001494	transvestism
MONDO:0001493	chronic pulmonary heart disease
MONDO:0001492	kyphoscoliotic heart disease
MONDO:0013466	orofacial cleft 13
MONDO:0013467	immunodeficiency due to ficolin3 deficiency
MONDO:0013464	episodic ataxia type 5
MONDO:0013465	achromatopsia 4
MONDO:0013468	retinitis pigmentosa 59
MONDO:0013469	retinitis pigmentosa 38
MONDO:0013462	fucosyltransferase 6 deficiency
MONDO:0013463	dextro-looped transposition of the great arteries 3
MONDO:0013460	osteogenesis imperfecta type 12
MONDO:0013461	inosine triphosphatase deficiency
MONDO:0001466	punctate epithelial keratoconjunctivitis
MONDO:0001465	superficial keratitis
MONDO:0001464	sigmoid colon cancer
MONDO:0001463	splenic flexure cancer
MONDO:0001469	cascade stomach
MONDO:0001468	synovial plica syndrome
MONDO:0001467	specific bursitis often of occupational origin
MONDO:0001462	descending colon cancer
MONDO:0001461	tinea corporis
MONDO:0001460	dyshormonogenic goiter
MONDO:0025431	keratoconjunctivitis, infectious
MONDO:0013455	hypertrophic cardiomyopathy 16
MONDO:0013456	constitutional megaloblastic anemia with severe neurologic disease
MONDO:0013453	Leber congenital amaurosis 8
MONDO:0013454	Leber congenital amaurosis 11
MONDO:0013459	osteogenesis imperfecta type 10
MONDO:0013457	Leber congenital amaurosis 15
MONDO:0013458	hyperuricemia-pulmonary hypertension-renal failure-alkalosis syndrome
MONDO:0013451	progressive myoclonic epilepsy type 5
MONDO:0013452	multisystemic smooth muscle dysfunction syndrome
MONDO:0013450	congenital stationary night blindness 1D
MONDO:0001477	aniridia
MONDO:0001476	coloboma
MONDO:0001475	neutropenia
MONDO:0001474	chronic salpingo-oophoritis
MONDO:0025425	hepatitis, infectious canine
MONDO:0001479	cutaneous diphtheria
MONDO:0001478	anisometropia
MONDO:0013439	congenital bile acid synthesis defect 3
MONDO:0001473	medulloadrenal hyperfunction
MONDO:0001472	testicular lymphoma
MONDO:0025420	gastroenteritis, transmissible, of swine
MONDO:0001471	histoplasmosis meningitis
MONDO:0001470	anal margin squamous cell carcinoma
MONDO:0013444	nephronophthisis 9
MONDO:0013445	complement component 9 deficiency
MONDO:0013442	nephronophthisis 12
MONDO:0013443	Seckel syndrome 5
MONDO:0013448	generalized epilepsy with febrile seizures plus, type 8
MONDO:0013449	Leber congenital amaurosis 7
MONDO:0013446	Leber congenital amaurosis 6
MONDO:0013447	retinitis pigmentosa 48
MONDO:0025419	furunculosis
MONDO:0013440	autosomal recessive limb-girdle muscular dystrophy type 2P
MONDO:0013441	asphyxiating thoracic dystrophy 4
MONDO:0025491	feline infectious peritonitis
MONDO:0025494	porcine reproductive and respiratory syndrome
MONDO:0025488	leukemia, feline
MONDO:0025487	murine acquired immunodeficiency syndrome
MONDO:0025489	enzootic bovine leukosis
MONDO:0025481	zoonosis
MONDO:0025484	simian acquired immunodeficiency syndrome
MONDO:0025483	mammary neoplasms, animal
MONDO:0025485	feline acquired immunodeficiency syndrome
MONDO:0025478	venereal tumors, veterinary
MONDO:0013499	Fanconi anemia complementation group P
MONDO:0013497	Okt4 epitope deficiency
MONDO:0013498	schizophrenia 15
MONDO:0013491	megalencephalic leukoencephalopathy with subcortical cysts 2B, remitting, with or without intellectual disability
MONDO:0013492	alopecia-intellectual disability syndrome 3
MONDO:0013490	megalencephalic leukoencephalopathy with subcortical cysts 2A
MONDO:0013495	autosomal recessive congenital ichthyosis 8
MONDO:0013496	IgA nephropathy, susceptibility to, 2
MONDO:0013493	acetyl-coa carboxylase deficiency
MONDO:0013494	PSMNSW
MONDO:0013488	lipodystrophy, partial, acquired, with low complement component c3, with or without glomerulonephritis
MONDO:0013489	autosomal recessive nonsyndromic deafness 89
MONDO:0013486	spinocerebellar ataxia type 32
MONDO:0013487	recurrent Neisseria infections due to factor D deficiency
MONDO:0013480	renal hypomagnesemia 6
MONDO:0013481	chromosome 13q14 deletion syndrome
MONDO:0013484	cataract 36
MONDO:0013485	spinocerebellar ataxia type 35
MONDO:0013482	Meckel syndrome, type 8
MONDO:0013483	obesity, hyperphagia, and developmental delay
MONDO:0003942	eosinophilic variant of chromophobe renal cell carcinoma
MONDO:0003943	central nervous system hibernoma
MONDO:0003944	endobronchial leiomyoma
MONDO:0003945	bone epithelioid hemangioma
MONDO:0003940	Kummell disease
MONDO:0003941	classic variant of chromophobe renal cell carcinoma
MONDO:0015928	secondary interstitial lung disease in childhood and adulthood associated with a connective tissue disease
MONDO:0015927	idiopathic eosinophilic pneumonia
MONDO:0015926	pneumoconiosis
MONDO:0015925	interstitial lung disease
MONDO:0015929	thoracic malformation
MONDO:0015931	rare urogenital tumor
MONDO:0015930	respiratory malformation
MONDO:0015935	extragonadal germinoma
MONDO:0015934	non-syndromic urogenital tract malformation of male and female
MONDO:0015933	non-syndromic urogenital tract malformation of male
MONDO:0015932	non-syndromic urogenital tract malformation of female
MONDO:0003939	muscle tissue disease
MONDO:0003935	oncocytic breast carcinoma
MONDO:0003936	invasive tubular breast carcinoma
MONDO:0003937	spondylitis
MONDO:0003938	bladder colonic type adenocarcinoma
MONDO:0003953	pediatric CNS choriocarcinoma
MONDO:0003954	angiokeratoma of Fordyce
MONDO:0003955	juvenile breast papillomatosis
MONDO:0003956	Baastrup syndrome
MONDO:0003950	nipple carcinoma
MONDO:0003951	scrotal hemangioma
MONDO:0003952	adult central nervous system choriocarcinoma
MONDO:0015917	malignant glioma
MONDO:0015916	rare neuroinflammatory or neuroimmunological disease
MONDO:0015915	cerebellar malformation
MONDO:0015914	primary orthostatic hypotension
MONDO:0015919	syndromic neurometabolic disease with non-X-linked intellectual disability
MONDO:0015918	rare neurodegenerative disease
MONDO:0015920	syndromic neurometabolic disease with X-linked intellectual disability
MONDO:0015924	pulmonary arterial hypertension
MONDO:0015923	acquired peripheral neuropathy
MONDO:0015922	channelopathy with epilepsy
MONDO:0015921	ARX-related epileptic encephalopathy
MONDO:0003946	vaginal villous adenoma
MONDO:0003947	hyper-IgM syndrome
MONDO:0003948	cerebral hemangioma
MONDO:0003949	cervical adenoma malignum
MONDO:0003920	gastric small cell carcinoma
MONDO:0003921	posterior foramen magnum meningioma
MONDO:0003922	ovarian clear cell malignant adenofibroma
MONDO:0003923	ethmoid sinus Schneiderian papilloma
MONDO:0015906	rare disorder with hypergonadotropic hypogonadism
MONDO:0015905	syndromic dyslipidemia
MONDO:0015904	rare hypolipidemia
MONDO:0015903	hyperalphalipoproteinemia
MONDO:0015909	aplastic anemia
MONDO:0015908	chromomycosis
MONDO:0015907	epimetaphyseal skeletal dysplasia
MONDO:0015913	rare thrombotic disease of hematologic origin
MONDO:0015912	macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss
MONDO:0015911	rare acquired hemolytic anemia
MONDO:0015910	rare constitutional hemolytic anemia
MONDO:0003917	heart lymphoma
MONDO:0003918	angiomatous meningioma
MONDO:0003919	inherited metabolic disorder
MONDO:0003913	choroid mixed cell melanoma
MONDO:0003914	inborn purine-pyrimidine metabolic disorder
MONDO:0003915	cortical thymoma
MONDO:0003916	overnutrition
MONDO:0003931	childhood optic tract astrocytoma
MONDO:0003932	childhood optic nerve glioma
MONDO:0003933	chest wall bone cancer
MONDO:0003934	breast apocrine carcinoma
MONDO:0003930	non-invasive bladder urothelial carcinoma
MONDO:0015902	major hypertriglyceridemia
MONDO:0015901	rare inherited hyperlipidemia
MONDO:0015900	hypoaldosteronism disease
MONDO:0003928	uterine corpus myxoid leiomyosarcoma
MONDO:0003929	vestibular micropapillomatosis
MONDO:0003924	adrenal cortex adenoma
MONDO:0003925	ethmoid sinus inverted papilloma
MONDO:0003926	neurilemmoma of the pleura
MONDO:0003927	posterior uveal melanoma
MONDO:0001323	infant gynecomastia
MONDO:0001322	pericardium cancer
MONDO:0003987	lung lymphoma
MONDO:0001321	scleral staphyloma
MONDO:0003988	sternum lymphoma
MONDO:0003989	polyembryoma of the ovary
MONDO:0001320	ring staphyloma
MONDO:0001327	pelvic muscle wasting
MONDO:0003982	bilateral breast carcinoma
MONDO:0003983	synchronous bilateral breast carcinoma
MONDO:0001326	dental pulp necrosis
MONDO:0001325	penile cancer
MONDO:0003984	internal auditory canal lipoma
MONDO:0003985	chest wall lymphoma
MONDO:0001324	hyperandrogenism
MONDO:0013309	chromosome 2p12-p11.2 deletion syndrome
MONDO:0013307	myopathy, lactic acidosis, and sideroblastic anemia 2
MONDO:0003980	schwannoma of jugular foramen
MONDO:0015969	rare genetic thyroid disease
MONDO:0013308	CBL-related disorder
MONDO:0003981	cervix small cell carcinoma
MONDO:0013312	retinitis pigmentosa 55
MONDO:0015975	hyper-IgM syndrome with susceptibility to opportunistic infections
MONDO:0015974	severe combined immunodeficiency
MONDO:0013313	ectodermal dysplasia-cutaneous syndactyly syndrome
MONDO:0013310	congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency
MONDO:0015973	rare genetic coagulation disorder
MONDO:0015972	rare constitutional anemia
MONDO:0013311	ectodermal dysplasia-syndactyly syndrome
MONDO:0013316	occult macular dystrophy
MONDO:0015979	hereditary predisposition to infections
MONDO:0013317	torsade-de-pointes syndrome with short coupling interval
MONDO:0015978	functional neutrophil defect
MONDO:0013314	retinitis pigmentosa 56
MONDO:0015977	agammaglobulinemia
MONDO:0013315	retinitis pigmentosa 57
MONDO:0015976	hyper-IgM syndrome without susceptibility to opportunistic infections
MONDO:0001319	bladder lateral wall cancer
MONDO:0001318	functional gastric disease
MONDO:0001317	phlyctenulosis
MONDO:0015971	rare genetic adrenal disease
MONDO:0003979	intrahepatic bile duct cystadenoma
MONDO:0015970	rare genetic parathyroid disease and phosphocalcic metabolism disorder
MONDO:0003997	colon Kaposi sarcoma
MONDO:0001334	hypertrichosis of eyelid
MONDO:0003998	vaginal tubular adenoma
MONDO:0001333	Patau syndrome
MONDO:0003999	juvenile pilocytic astrocytoma
MONDO:0001332	palindromic rheumatism
MONDO:0001331	conjunctival deposit
MONDO:0003993	childhood vagina botryoid rhabdomyosarcoma
MONDO:0001338	acute apical periodontitis
MONDO:0003994	botryoid-type embryonal rhabdomyosarcoma of the vagina
MONDO:0001337	inflamed seborrheic keratosis
MONDO:0001336	familial hyperlipidemia
MONDO:0003995	vulvar childhood botryoid-type embryonal rhabdomyosarcoma
MONDO:0001335	hypotrichosis of eyelid
MONDO:0003996	basal ganglia disease
MONDO:0003990	malignant breast myoepithelioma
MONDO:0015959	inherited syndrome with bone tumors as a major feature
MONDO:0003991	villoglandular endometrial endometrioid adenocarcinoma
MONDO:0015958	rare genetic bone disease
MONDO:0003992	childhood botryoid rhabdomyosarcoma
MONDO:0001330	presbyopia
MONDO:0013301	aromatase deficiency
MONDO:0015964	obsolete rare genetic palpebral, lacrimal system and conjunctival disease
MONDO:0013302	nephronophthisis 11
MONDO:0015963	inherited renal tumor
MONDO:0015962	inherited renal tubular disease
MONDO:0013300	commissural facial cleft
MONDO:0015961	genetic head and neck malformation
MONDO:0013305	autosomal dominant nonsyndromic deafness 51
MONDO:0015968	rare genetic hypothalamic or pituitary disease
MONDO:0013306	combined oxidative phosphorylation defect type 7
MONDO:0015967	monogenic diabetes
MONDO:0013303	autoimmune disease, susceptibility to, 6
MONDO:0015966	hereditary eye tumor
MONDO:0013304	von Willebrand disease 2
MONDO:0015965	rare genetic refraction anomaly
MONDO:0001329	accommodative spasm
MONDO:0001328	thyroid hormone resistance syndrome
MONDO:0015960	rare genetic developmental defect during embryogenesis
MONDO:0001301	rumination disorder
MONDO:0003964	myositis ossificans
MONDO:0003965	Capgras syndrome
MONDO:0001300	autonomic neuropathy
MONDO:0003966	testicular monophasic choriocarcinoma
MONDO:0003967	synchronous multifocal osteogenic sarcoma
MONDO:0003960	pulmonary large cell neuroendocrine carcinoma
MONDO:0001305	laryngostenosis
MONDO:0001304	benign hypertensive renal disease
MONDO:0003961	cervical large cell neuroendocrine carcinoma
MONDO:0003962	Froelich syndrome
MONDO:0001303	abnormal pupillary function
MONDO:0003963	diffuse infiltrative lymphocytosis syndrome
MONDO:0001302	hypertensive heart disease
MONDO:0015949	rare genetic subcutaneous tissue disorder
MONDO:0015948	rare genetic skin vascular disorder
MONDO:0015947	inherited ichthyosis
MONDO:0015953	genetic central nervous system and retinal vascular disease
MONDO:0015952	genetic neurodegenerative disease
MONDO:0015951	hereditary photodermatosis
MONDO:0015950	inherited skin tumor
MONDO:0015957	rare genetic movement disorder
MONDO:0015956	rare hereditary ataxia
MONDO:0015955	rare genetic epilepsy
MONDO:0015954	rare genetic headache disorder
MONDO:0003957	adult pineoblastoma
MONDO:0003958	childhood central nervous system immature teratoma
MONDO:0003959	breast large cell neuroendocrine carcinoma
MONDO:0001312	acute serous otitis media
MONDO:0003975	Littre gland carcinoma
MONDO:0003976	malignant type AB thymoma
MONDO:0001311	Chandler syndrome
MONDO:0001310	Bowman's membrane folds or rupture
MONDO:0003977	fibrillary astrocytoma
MONDO:0003978	colon small cell neuroendocrine carcinoma
MONDO:0001316	streptococcal meningitis
MONDO:0003971	gastric pylorus carcinoma
MONDO:0001315	neurocirculatory asthenia
MONDO:0003972	gastric body carcinoma
MONDO:0001314	chondrocalcinosis
MONDO:0003973	tubular variant testicular seminoma
MONDO:0001313	acute allergic serous otitis media
MONDO:0003974	malignant triton tumor
MONDO:0015939	systemic autoimmune disease
MONDO:0015938	systemic disease
MONDO:0015937	rare inflammatory eye disease
MONDO:0003970	gastric fundus carcinoma
MONDO:0015936	rare tumor of endocrine glands
MONDO:0015942	frontometaphyseal dysplasia
MONDO:0015941	epiphyseal dysplasia-hearing loss-dysmorphism syndrome
MONDO:0015940	rare rheumatologic disease
MONDO:0015946	rare genetic epidermal disorder
MONDO:0015945	polymalformative genetic syndrome with increased risk of developing cancer
MONDO:0015944	axial mesodermal dysplasia spectrum
MONDO:0015943	eosinophilic granulomatosis with polyangiitis
MONDO:0001309	oculomotor nerve paralysis
MONDO:0001308	corneal deposit
MONDO:0001307	corneal abscess
MONDO:0001306	recurrent corneal erosion
MONDO:0003968	asynchronous multifocal osteogenic sarcoma
MONDO:0003969	amphetamine abuse
MONDO:0003900	connective tissue disease
MONDO:0003901	cerebellar hemangioblastoma
MONDO:0003910	mixed cell uveal melanoma
MONDO:0003911	ciliary body mixed cell melanoma
MONDO:0003912	malignant ciliary body melanoma
MONDO:0003906	ovarian yolk sac tumor, hepatoid pattern
MONDO:0003907	ovarian yolk sac tumor, polyvesicular vitelline pattern
MONDO:0003908	clivus meningioma
MONDO:0003909	Bartholin gland adenomyoma
MONDO:0003902	brain stem hemangioblastoma
MONDO:0003903	benign vaginal mixed tumor
MONDO:0003904	lung occult squamous cell carcinoma
MONDO:0003905	ovarian yolk sac tumor, glandular pattern
MONDO:0025397	canine distemper
MONDO:0025389	brucellosis, bovine
MONDO:0025381	avian leukosis
MONDO:0025382	sarcoma, avian
MONDO:0025385	bluetongue
MONDO:0001367	chronic congestive splenomegaly
MONDO:0001366	splenic sequestration
MONDO:0001365	necrosis of ear ossicle
MONDO:0001364	regular astigmatism
MONDO:0001369	chronic laryngitis
MONDO:0001368	phthisical cornea
MONDO:0001363	blind hypertensive eye
MONDO:0001362	leukocoria
MONDO:0001361	spontaneous ocular nystagmus
MONDO:0001360	blind hypotensive eye
MONDO:0013356	vesicoureteral reflux 3
MONDO:0040964	superimposed infection
MONDO:0013357	chromosome 17q11.2 deletion syndrome, 1.4Mb
MONDO:0013354	spastic ataxia 4
MONDO:0013355	congenital dyserythropoietic anemia type 4
MONDO:0013358	Seckel syndrome 4
MONDO:0013359	familial hyperaldosteronism type III
MONDO:0013352	intellectual disability-severe speech delay-mild dysmorphism syndrome
MONDO:0013353	intellectual disability, anterior maxillary protrusion, and strabismus
MONDO:0013350	mitochondrial DNA depletion syndrome 4b
MONDO:0013351	infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly
MONDO:0001378	urachus cancer
MONDO:0001377	vitreous syneresis
MONDO:0001376	urinary bladder anterior wall cancer
MONDO:0001375	bladder trigone cancer
MONDO:0001379	ureteric orifice cancer
MONDO:0001370	pericardial effusion
MONDO:0001374	bladder sarcoma
MONDO:0001373	urinary bladder posterior wall cancer
MONDO:0001372	bladder neck cancer
MONDO:0001371	protein-energy malnutrition
MONDO:0013345	d-2-hydroxyglutaric aciduria 2
MONDO:0013346	brain calcification, Rajab type
MONDO:0013343	C1Q deficiency
MONDO:0013344	migraine, with or without aura, susceptibility to, 13
MONDO:0013349	ALG11-CDG
MONDO:0013347	gastric cancer
MONDO:0013348	cone-rod dystrophy 15
MONDO:0013341	methylmalonic acidemia due to transcobalamin receptor defect
MONDO:0013342	hereditary spastic paraplegia 48
MONDO:0013340	Parkinson disease 5, autosomal dominant, susceptibility to
MONDO:0001345	antidepressant type abuse
MONDO:0001344	neonatal diabetes mellitus
MONDO:0001343	impaired renal function disease
MONDO:0001342	dysgammaglobulinemia
MONDO:0001349	odontoclasia
MONDO:0001348	Lyme disease
MONDO:0001347	facioscapulohumeral muscular dystrophy
MONDO:0001346	distal muscular dystrophy
MONDO:0013329	familial clubfoot due to 17q23.1q23.2 microduplication
MONDO:0001341	selective IgA deficiency disease
MONDO:0001340	heart cancer
MONDO:0015997	ectopia lentis-chorioretinal dystrophy-myopia syndrome
MONDO:0013334	cocoon syndrome
MONDO:0013335	tuberculin skin test reactivity, absence of
MONDO:0015996	systemic capillary leak syndrome
MONDO:0015995	melorheostosis with osteopoikilosis
MONDO:0013332	brachydactyly, type A1, with short stature, scoliosis, microcephaly, ptosis, hearing loss, and intellectual disability
MONDO:0015994	muscular dystrophy-white matter spongiosis syndrome
MONDO:0013333	odontoid hypoplasia
MONDO:0013338	Charcot-Marie-Tooth disease recessive intermediate B
MONDO:0013339	dilated cardiomyopathy 1GG
MONDO:0015999	primary pigmented nodular adrenocortical disease
MONDO:0013336	chromosome 19p13.13 deletion syndrome
MONDO:0013337	neuropathy, hereditary sensory and autonomic, type 1C
MONDO:0015998	isolated ectopia lentis
MONDO:0001339	portal vein thrombosis
MONDO:0015993	cone-rod dystrophy
MONDO:0013330	agenesis of the corpus callosum and congenital lymphedema
MONDO:0013331	factor 5 and Factor VIII, combined deficiency of, 2
MONDO:0015992	progressive cone dystrophy
MONDO:0015991	citrullinemia
MONDO:0015990	focal, segmental or multifocal dystonia
MONDO:0001356	iron deficiency anemia
MONDO:0001355	ocular siderosis
MONDO:0025303	anaplasmosis
MONDO:0001354	acute endophthalmitis
MONDO:0001353	Bordetella parapertussis infectious disease
MONDO:0001359	Kohler disease
MONDO:0001358	bronchial disease
MONDO:0001357	hypochromic anemia
MONDO:0013318	early repolarization associated with ventricular fibrillation
MONDO:0013319	chromosome 4Q32.1-q32.2 triplication syndrome
MONDO:0001352	round ligament malignant neoplasm
MONDO:0001351	uterine adnexa cancer
MONDO:0001350	parametrium malignant neoplasm
MONDO:0013323	cranioectodermal dysplasia 2
MONDO:0015986	bilateral renal agenesis
MONDO:0015985	bone dysplasia, Azouz type
MONDO:0013324	lymphedema-posterior choanal atresia syndrome
MONDO:0015984	rare genetic immune disease
MONDO:0013321	forsythe-wakeling syndrome
MONDO:0015983	rare genetic syndromic intellectual disability
MONDO:0013322	epilepsy, familial adult myoclonic, 3
MONDO:0013327	primary hyperoxaluria type 3
MONDO:0013328	retinitis pigmentosa 58
MONDO:0015989	congenital valvular dysplasia
MONDO:0013325	COG5-CDG
MONDO:0015988	multicystic dysplastic kidney
MONDO:0013326	Senior-Loken syndrome 7
MONDO:0040998	Pasteurella multocida infectious disease
MONDO:0015987	scimitar syndrome
MONDO:0015982	rare genetic intellectual disability
MONDO:0013320	chromosome 16p12.2-p11.2 deletion syndrome
MONDO:0015981	inherited gynecological tumor
MONDO:0015980	rare genetic gynecological and obstetrical diseases
MONDO:0025377	African swine fever
MONDO:0025370	urogenital neoplasm
MONDO:0025371	Parvoviridae infectious disease
MONDO:0025376	African horse sickness
MONDO:0013398	acne inversa, familial, 3
MONDO:0013399	cardiomyopathy, dilated, 1T
MONDO:0040923	late latent syphilis
MONDO:0040922	latent early syphilis
MONDO:0013392	autosomal recessive spinocerebellar ataxia 10
MONDO:0013393	distal 7q11.23 microdeletion syndrome
MONDO:0013390	autosomal recessive limb-girdle muscular dystrophy type 2Q
MONDO:0013391	sterol carrier protein 2 deficiency
MONDO:0040925	latent yaws
MONDO:0013396	chromosome 1p32-p31 deletion syndrome
MONDO:0013397	acne inversa, familial, 2
MONDO:0013394	porencephaly-microcephaly-bilateral congenital cataract syndrome
MONDO:0013395	retinitis pigmentosa 4
MONDO:0025369	Nairobi sheep disease
MONDO:0013389	developmental and epileptic encephalopathy, 12
MONDO:0013387	developmental and epileptic encephalopathy, 7
MONDO:0013388	developmental and epileptic encephalopathy, 11
MONDO:0013381	neuropathy, hereditary sensory, type 1D
MONDO:0013382	progressive demyelinating neuropathy with bilateral striatal necrosis
MONDO:0013380	LEOPARD syndrome 3
MONDO:0013385	Treacher Collins syndrome 2
MONDO:0013386	autosomal recessive nonsyndromic deafness 74
MONDO:0013383	Hirschsprung disease, susceptibility to, 3
MONDO:0013384	Hirschsprung disease, susceptibility to, 4
MONDO:0025356	azoospermia, obstructive, with nephrolithiasis
MONDO:0001389	congenital coronary artery anomaly
MONDO:0001388	glans penis cancer
MONDO:0001387	penile sarcoma
MONDO:0001386	visual epilepsy
MONDO:0001381	bladder lymphoma
MONDO:0001380	bladder dome cancer
MONDO:0001385	cortical blindness
MONDO:0001384	myopia
MONDO:0025351	multiple congenital anomalies-neurodevelopmental syndrome, x-linked
MONDO:0001383	degenerative myopia
MONDO:0025354	spermatogenic failure, X-linked, 3
MONDO:0001382	hepatorenal syndrome
MONDO:0025353	developmental and epileptic encephalopathy, 90
MONDO:0013378	orofacial cleft 10
MONDO:0013379	Noonan syndrome 7
MONDO:0013376	microphthalmia, isolated, with coloboma 6
MONDO:0013377	isolated microphthalmia 7
MONDO:0013370	long QT syndrome 6
MONDO:0013371	dilated cardiomyopathy 1U
MONDO:0013374	supernumerary der(22)t(8;22) syndrome
MONDO:0013375	Klippel-Feil syndrome 3, autosomal dominant
MONDO:0013372	long QT syndrome 5
MONDO:0013373	dilated cardiomyopathy 1V
MONDO:0001399	ureter leiomyoma
MONDO:0001398	ureter benign neoplasm
MONDO:0001397	mononeuropathy
MONDO:0001392	monocular exotropia
MONDO:0001391	indeterminate leprosy
MONDO:0001390	transient refractive change
MONDO:0001396	abnormal threshold of rods
MONDO:0001395	macular keratitis
MONDO:0001394	chronic erythremia
MONDO:0001393	peripheral focal chorioretinitis
MONDO:0013367	long QT syndrome 2
MONDO:0013368	mammary-digital-nail syndrome
MONDO:0013365	autosomal recessive nonsyndromic deafness 83
MONDO:0013366	spondylocostal dysostosis 4, autosomal recessive
MONDO:0013369	hypertrophic cardiomyopathy 7
MONDO:0013360	brachyolmia, Maroteaux type
MONDO:0013363	chromosome 2q31.1 duplication syndrome
MONDO:0013364	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
MONDO:0013361	congenital prothrombin deficiency
MONDO:0013362	THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome
MONDO:0003821	ovarian biphasic or triphasic teratoma
MONDO:0003822	non-invasive bladder papillary urothelial neoplasm
MONDO:0003823	transient hypogammaglobulinemia of infancy
MONDO:0003824	hereditary kidney oncocytoma
MONDO:0003820	mature ovarian teratoma
MONDO:0015807	myopic macular degeneration
MONDO:0015806	adult intestinal botulism
MONDO:0015805	intestinal botulism
MONDO:0015804	infant botulism
MONDO:0015809	localized pagetoid reticulosis
MONDO:0015808	folliculotropic mycosis fungoides
MONDO:0015810	primary cutaneous CD4+ small/medium-sized pleomorphic T-cell lymphoma
MONDO:0015814	primary cutaneous follicle center lymphoma
MONDO:0015813	primary cutaneous marginal zone B-cell lymphoma
MONDO:0015812	primary cutaneous gamma/delta-positive T-cell lymphoma
MONDO:0015811	primary cutaneous aggressive epidermotropic CD8+ T-cell lymphoma
MONDO:0003818	childhood mature teratoma of the ovary
MONDO:0003819	childhood teratoma of the ovary
MONDO:0003814	gastric diffuse adenocarcinoma
MONDO:0003815	Cronkhite-Canada syndrome
MONDO:0003816	articular cartilage disease
MONDO:0003817	peritoneal serous papillary adenocarcinoma
MONDO:0003832	complement deficiency
MONDO:0003833	severe combined immunodeficiency
MONDO:0003834	gastric cardia carcinoma
MONDO:0003835	gastric cardia adenocarcinoma
MONDO:0003830	type 1 papillary adenoma of the kidney
MONDO:0003831	type 2 papillary adenoma of the kidney
MONDO:0015803	wound botulism
MONDO:0015802	autosomal dominant non-syndromic intellectual disability
MONDO:0015801	hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation
MONDO:0015800	osteosclerosis-developmental delay-craniosynostosis syndrome
MONDO:0003829	chromophil adenoma of the kidney
MONDO:0003825	kidney oncocytoma
MONDO:0003826	mediastinum seminoma
MONDO:0003827	transient hypogammaglobulinemia
MONDO:0003828	growth hormone-producing pituitary gland carcinoma
MONDO:0003800	conventional malignant hemangiopericytoma
MONDO:0003801	corneal intraepithelial neoplasm
MONDO:0003802	cornea cancer
MONDO:0003810	bladder diffuse clear cell adenocarcinoma
MONDO:0003811	ovarian seromucinous tumor
MONDO:0003812	ovarian endometrial cancer
MONDO:0003813	ovarian papillary tumor
MONDO:0003807	follicular thyroid adenoma
MONDO:0003808	mediastinal extraskeletal osteosarcoma
MONDO:0003809	malignant mediastinum hemangiopericytoma
MONDO:0003803	aortic valve disease
MONDO:0003804	blood protein disease
MONDO:0003805	malignant pericardial mesothelioma
MONDO:0003806	thyroid hyalinizing trabecular adenoma
MONDO:0001202	prostatic cyst
MONDO:0003865	acral lentiginous melanoma
MONDO:0003866	liver extraskeletal osteosarcoma
MONDO:0001200	secondary hypertension
MONDO:0003867	diffuse meningeal melanocytosis
MONDO:0003868	anterior foramen magnum meningioma
MONDO:0003861	vulvar eccrine adenocarcinoma
MONDO:0001206	aqueous misdirection
MONDO:0003862	melanotic psammomatous malignant peripheral nerve sheath tumor
MONDO:0001205	hypersecretion glaucoma
MONDO:0003863	malignant melanocytic neoplasm of the peripheral nerve sheath
MONDO:0001204	esophagus sarcoma
MONDO:0003864	chronic lymphocytic leukemia/small lymphocytic lymphoma
MONDO:0001203	prolapse of lacrimal gland
MONDO:0015849	longitudinal vaginal septum
MONDO:0003860	cerebellopontine angle meningioma
MONDO:0015848	septate vagina
MONDO:0015854	supernumerary breasts
MONDO:0015853	deficient breast volume or number
MONDO:0015852	excess breast volume or number
MONDO:0015851	rare breast malformation
MONDO:0015858	rare non-malformative breast disease
MONDO:0015857	rare non-malformative gynecologic or obstetric disease
MONDO:0015856	syndromic breast hypoplasia/aplasia
MONDO:0015855	isolated congenital breast hypoplasia/aplasia
MONDO:0015850	transverse vaginal septum
MONDO:0003858	anterior optic tract meningioma
MONDO:0003859	bilateral meningioma of optic nerve
MONDO:0003876	eyelid carcinoma
MONDO:0001213	serous glue ear
MONDO:0001212	non-suppurative otitis media
MONDO:0003877	cervical adenoid basal carcinoma
MONDO:0003878	malignant choroid melanoma
MONDO:0001211	total internal ophthalmoplegia
MONDO:0001210	enophthalmos
MONDO:0003879	ovarian endometrioid adenocarcinofibroma
MONDO:0001217	pseudomembranous conjunctivitis
MONDO:0003872	ovarian papillary cystadenoma
MONDO:0003873	ovarian surface papilloma
MONDO:0001216	pulp degeneration
MONDO:0001215	allescheriosis
MONDO:0003874	ovarian serous surface papillary adenocarcinoma
MONDO:0001214	acute conjunctivitis
MONDO:0003875	childhood central nervous system mature teratoma
MONDO:0015839	septate uterus
MONDO:0015838	cordiform uterus
MONDO:0003870	childhood brainstem astrocytoma
MONDO:0015837	Unicervical bicornuate uterus
MONDO:0003871	metanephric adenoma
MONDO:0015843	uterine hypoplasia
MONDO:0015842	bicornuate uterus
MONDO:0015841	partial septate uterus
MONDO:0015840	complete septate uterus
MONDO:0015847	rare vaginal malformation
MONDO:0015846	syndromic uterovaginal malformation
MONDO:0015845	uterine cervical aplasia and agenesis
MONDO:0015844	agenesis and aplasia of uterine body
MONDO:0001209	common wart
MONDO:0001208	acute respiratory failure
MONDO:0001207	neonatal respiratory failure
MONDO:0003869	childhood brain stem glioma
MONDO:0003843	cerebral hemisphere lipoma
MONDO:0003844	central nervous system lipoma
MONDO:0003845	corpus callosum lipoma
MONDO:0003846	viral esophagitis
MONDO:0003840	epicardium lipoma
MONDO:0003841	heart lipoma
MONDO:0003842	childhood cerebellar astrocytic neoplasm
MONDO:0015829	non-syndromic uterovaginal malformation
MONDO:0015828	uterovaginal malformation
MONDO:0015827	distal renal tubular acidosis
MONDO:0015826	autosomal dominant spondylocostal dysostosis
MONDO:0015832	true unicornuate uterus
MONDO:0015831	unilateral aplasia of the mullerian ducts
MONDO:0015830	partial bilateral aplasia of the mullerian ducts
MONDO:0015836	Bicervical bicornuate uterus with patent cervix and vagina
MONDO:0015835	Bicervical bicornuate uterus and blind hemivagina
MONDO:0015834	didelphys uterus
MONDO:0015833	pseudounicornuate uterus
MONDO:0003836	malignant thyroid stimulating hormone producing neoplasm of pituitary gland
MONDO:0003837	TSH producing pituitary tumor
MONDO:0003838	malignant ACTH producing neoplasm of pituitary gland
MONDO:0003839	ovarian mucinous adenocarcinofibroma
MONDO:0003854	tibial adamantinoma
MONDO:0003855	immature teratoma of ovary
MONDO:0003856	adult malignant hemangiopericytoma
MONDO:0003857	adult intracranial malignant hemangiopericytoma
MONDO:0003850	clivus chondroid chordoma
MONDO:0003851	ovarian fetiform teratoma
MONDO:0003852	ovarian solid teratoma
MONDO:0003853	Bartholin gland adenocarcinoma
MONDO:0015818	aggressive primary cutaneous B-cell lymphoma
MONDO:0015817	aggressive primary cutaneous T-cell lymphoma
MONDO:0015816	indolent primary cutaneous T-cell lymphoma
MONDO:0015815	primary cutaneous diffuse large B-cell lymphoma, leg type
MONDO:0015819	indolent primary cutaneous B-cell lymphoma
MONDO:0015821	mycosis fungoides and variants
MONDO:0015820	primary cutaneous B-cell lymphoma
MONDO:0015825	obesity due to congenital leptin resistance
MONDO:0015824	oculomaxillofacial dysostosis
MONDO:0015823	primary immunodeficiency due to a defect in adaptive immunity
MONDO:0015822	acquired neutropenia
MONDO:0003847	Mendelian disease
MONDO:0003848	ectopic thymus
MONDO:0003849	clivus chordoma
MONDO:0025293	poult enteritis mortality syndrome
MONDO:0025294	tick-borne infectious disease
MONDO:0013290	agammaglobulinemia 5, autosomal dominant
MONDO:0025271	trypanosomiasis, bovine
MONDO:0025270	toxoplasmosis, non-human animal
MONDO:0013299	chromosome 6q11-q14 deletion syndrome
MONDO:0013293	isolated microphthalmia 6
MONDO:0013294	atopic dermatitis 8
MONDO:0013291	glycogen storage disease XV
MONDO:0013292	chromosome 4q21 deletion syndrome
MONDO:0013297	autosomal dominant limb-girdle muscular dystrophy type 1H
MONDO:0013298	chromosome 17q21.31 duplication syndrome
MONDO:0013295	atopic dermatitis 9
MONDO:0013296	myeloid neoplasm associated with FGFR1 rearrangement
MONDO:0025263	strongyle infections, equine
MONDO:0013288	agammaglobulinemia 3, autosomal recessive
MONDO:0013289	agammaglobulinemia 4, autosomal recessive
MONDO:0013282	alpha 1-antitrypsin deficiency
MONDO:0013283	immunodeficiency, common variable, 3
MONDO:0013280	myxoid liposarcoma
MONDO:0013281	COG4-CDG
MONDO:0013286	immunodeficiency, common variable, 6
MONDO:0013287	agammaglobulinemia 2, autosomal recessive
MONDO:0013284	immunodeficiency, common variable, 4
MONDO:0013285	immunodeficiency, common variable, 5
MONDO:0049223	osteogenesis imperfecta, type 19
MONDO:0049222	intellectual disability, X-linked 107
MONDO:0049221	myopia 26, X-linked, female-limited
MONDO:0037250	childhood testicular neoplasm
MONDO:0037251	congestive splenomegaly
MONDO:0037252	thecoma
MONDO:0037253	ovarian thecoma
MONDO:0037254	transitional cell neoplasm
MONDO:0037255	ovarian serous tumor
MONDO:0037256	serous neoplasm
MONDO:0001246	typhus
MONDO:0001245	microcytic anemia
MONDO:0001244	vitamin K deficiency hemorrhagic disease
MONDO:0001243	disseminated intravascular coagulation
MONDO:0001249	trachoma
MONDO:0001248	rabies
MONDO:0001247	social phobia
MONDO:0001242	disseminated intravascular coagulation in newborn
MONDO:0001241	transient neonatal neutropenia
MONDO:0001240	neonatal anemia
MONDO:0015898	adrenogenital syndrome
MONDO:0013235	pancreatic cancer, susceptibility to, 2
MONDO:0015897	rare hyperparathyroidism
MONDO:0013236	pancreatic cancer, susceptibility to, 3
MONDO:0015896	rare hypoparathyroidism
MONDO:0013233	spondyloepimetaphyseal dysplasia, Handigodu type
MONDO:0013234	hypokalemic periodic paralysis, type 2
MONDO:0015895	syndrome with hypoparathyroidism
MONDO:0013239	hereditary spastic paraplegia 41
MONDO:0013237	susceptibility to mononeuropathy of the median nerve, mild
MONDO:0013238	chromosome 17q23.1-q23.2 deletion syndrome
MONDO:0015899	rare primary hyperaldosteronism
MONDO:0015890	rare disorder with congenital hypogonadotropic hypogonadism
MONDO:0013231	Leber congenital amaurosis 14
MONDO:0015894	rare hyperthyroidism
MONDO:0015893	rare hypothyroidism
MONDO:0013232	brachydactylous dwarfism, Mseleni type
MONDO:0015892	growth hormone insensitivity syndrome
MONDO:0013230	epilepsy, hot water, 2
MONDO:0015891	hypogonadotropic hypogonadism associated with other endocrinopathies
MONDO:0001257	retinal microaneurysm
MONDO:0001256	arteriovenous hemangioma/malformation
MONDO:0001255	ventilation pneumonitis
MONDO:0001254	peripheral scars of retina
MONDO:0001259	pituitary gland infarction
MONDO:0001258	vertebral artery occlusion
MONDO:0013219	hypophosphatemic rickets, autosomal recessive, 2
MONDO:0001253	solar retinopathy
MONDO:0001252	Plummer disease
MONDO:0001251	chronic apical periodontitis
MONDO:0001250	keratomalacia
MONDO:0013224	rhabdoid tumor predisposition syndrome 2
MONDO:0015887	rare diabetes mellitus type 2
MONDO:0013225	congenital generalized lipodystrophy type 4
MONDO:0015886	rare diabetes mellitus type 1
MONDO:0013222	Miyoshi muscular dystrophy 3
MONDO:0015885	rare insulin-resistance syndrome
MONDO:0015884	autosomal dominant hypohidrotic ectodermal dysplasia
MONDO:0013223	autosomal recessive spondylometaphyseal dysplasia, Megarbane type
MONDO:0013228	spondylo-megaepiphyseal-metaphyseal dysplasia
MONDO:0013229	hot water reflex epilepsy
MONDO:0015889	rare hypothalamic or pituitary disease
MONDO:0013226	combined immunodeficiency with faciooculoskeletal anomalies
MONDO:0015888	other rare diabetes mellitus
MONDO:0013227	congenital plasminogen activator inhibitor type 1 deficiency
MONDO:0013220	hemochromatosis type 2B
MONDO:0015883	hidrotic ectodermal dysplasia, Halal type
MONDO:0015882	rare tumor of pancreas
MONDO:0013221	Miyoshi muscular dystrophy 2
MONDO:0015881	gastroesophageal tumor
MONDO:0015880	syndromic diaphragmatic or thoracic malformation
MONDO:0003887	ovarian mucinous adenofibroma
MONDO:0001224	Angelucci syndrome
MONDO:0003888	childhood testicular mixed embryonal carcinoma and teratoma
MONDO:0001223	parathyroid gland disease
MONDO:0003889	infiltrating bladder urothelial carcinoma, clear cell variant
MONDO:0001222	congenital T-cell immunodeficiency
MONDO:0001221	esophageal varices
MONDO:0003883	cerebellar liponeurocytoma
MONDO:0001228	conjunctival folliculosis
MONDO:0003884	lipoma of the rectum
MONDO:0001227	chronic tympanitis
MONDO:0003885	colorectal lipoma
MONDO:0001226	acute contagious conjunctivitis
MONDO:0001225	opioid abuse
MONDO:0003886	mucinous cystadenofibroma
MONDO:0003880	ceruminous carcinoma
MONDO:0003881	vulvar apocrine adenocarcinoma
MONDO:0013208	cirrhosis - dystonia - polycythemia - hypermanganesemia syndrome
MONDO:0013209	non-alcoholic fatty liver disease
MONDO:0003882	central nervous system fibrosarcoma
MONDO:0001220	hypoparathyroidism
MONDO:0040872	non-psychogenic polydipsia
MONDO:0040871	psychogenic polydipsia
MONDO:0040870	primary polydipsia
MONDO:0013213	hearing loss, cisplatin-induced, susceptibility to
MONDO:0015876	rare vulvovaginal tumor
MONDO:0015875	rare non-malformative uterine adnexal disease
MONDO:0013214	bile acid malabsorption, primary
MONDO:0013211	dilated cardiomyopathy 1FF
MONDO:0015874	benign ductal tumor of breast
MONDO:0013212	Charcot-Marie-Tooth disease axonal type 2N
MONDO:0015873	Paget disease of the nipple
MONDO:0013217	Diamond-Blackfan anemia 10
MONDO:0015879	non-syndromic diaphragmatic or thoracic malformation
MONDO:0013218	exudative vitreoretinopathy 5
MONDO:0013215	autosomal recessive nonsyndromic deafness 79
MONDO:0015878	rare disease with autism
MONDO:0015877	malformative syndrome with dentinogenesis imperfecta
MONDO:0013216	Diamond-Blackfan anemia 9
MONDO:0001219	serous conjunctivitis except viral
MONDO:0001218	acute laryngopharyngitis
MONDO:0015872	giant adenofibroma of the breast
MONDO:0015871	benign breast phyllodes tumor
MONDO:0013210	autosomal recessive nonsyndromic deafness 25
MONDO:0015870	rare malignant breast tumor
MONDO:0001235	appendix cancer
MONDO:0003898	pediatric myxoid chondrosarcoma
MONDO:0001234	adhesive otitis media
MONDO:0003899	adult myxoid chondrosarcoma
MONDO:0001233	orbital tenonitis
MONDO:0001232	orbital osteomyelitis
MONDO:0003894	mediastinal melanocytic neurilemmoma
MONDO:0001239	anemia of prematurity
MONDO:0003895	periosteal osteogenic sarcoma
MONDO:0001238	polycythemia neonatorum
MONDO:0003896	breast capillary hemangioma
MONDO:0001237	appendix lymphoma
MONDO:0003897	breast epithelioid hemangioma
MONDO:0001236	appendiceal neoplasm
MONDO:0003890	infiltrating bladder urothelial carcinoma
MONDO:0003891	bladder signet ring cell adenocarcinoma
MONDO:0003892	acinar lung adenocarcinoma
MONDO:0015859	rare non-malformative uterovaginal or vulvovaginal disease
MONDO:0003893	rete testis adenoma
MONDO:0001231	orbital periostitis
MONDO:0001230	acute orbital inflammation
MONDO:0015865	benign tumor of fallopian tubes
MONDO:0013202	Waardenburg syndrome type 4C
MONDO:0013203	corneal dystrophy, Fuchs endothelial, 3
MONDO:0015864	mixed germ cell tumor
MONDO:0013200	hypertrophic cardiomyopathy 15
MONDO:0015863	polyembryoma
MONDO:0013201	Waardenburg syndrome type 4B
MONDO:0015862	embryonal carcinoma
MONDO:0015869	rare benign breast tumor
MONDO:0013206	corneal dystrophy, Fuchs endothelial, 6
MONDO:0013207	corneal dystrophy, fuchs endothelial, 7
MONDO:0015868	rare breast tumor
MONDO:0015867	vaginal carcinoma
MONDO:0013204	corneal dystrophy, Fuchs endothelial, 4
MONDO:0015866	malignant tumor of fallopian tubes
MONDO:0013205	corneal dystrophy, fuchs endothelial, 5
MONDO:0001229	small intestine diverticulitis
MONDO:0015861	rare uterine adnexal tumor
MONDO:0015860	anomaly of puberty or/and menstrual cycle
MONDO:0001289	endometriosis of ovary
MONDO:0001288	endometriosis of rectovaginal septum and vagina
MONDO:0001287	endometriosis in cutaneous scar
MONDO:0001282	fallopian tube endometriosis
MONDO:0001281	alternating exotropia
MONDO:0001280	choroiditis
MONDO:0001286	exotropia
MONDO:0001285	endometriosis of pelvic peritoneum
MONDO:0001284	endometriosis of intestine
MONDO:0001283	endosalpingiosis
MONDO:0013279	long QT syndrome 13
MONDO:0013277	developmental and epileptic encephalopathy, 5
MONDO:0013278	lymphatic malformation 3
MONDO:0013271	frontonasal dysplasia - severe microphthalmia - severe facial clefting syndrome
MONDO:0013272	chromosome 14q11-q22 deletion syndrome
MONDO:0013270	Rett syndrome, congenital variant
MONDO:0013275	hemolytic anemia due to glucophosphate isomerase deficiency
MONDO:0013276	Reynolds syndrome
MONDO:0013273	chromosome 16p13.3 duplication syndrome
MONDO:0013274	retinitis pigmentosa 51
MONDO:0001299	diabetic autonomic neuropathy
MONDO:0001298	congenital mitral valve insufficiency
MONDO:0001293	subglottis cancer
MONDO:0001292	autonomic nervous system disease
MONDO:0001291	brain compression
MONDO:0001290	allergic cutaneous vasculitis
MONDO:0001297	cardiac tamponade
MONDO:0001296	acquired night blindness
MONDO:0001295	idiopathic peripheral autonomic neuropathy
MONDO:0001294	Horner syndrome
MONDO:0013268	frontonasal dysplasia with alopecia and genital anomaly
MONDO:0013269	autosomal recessive nonsyndromic deafness 91
MONDO:0013266	intellectual disability, autosomal dominant 20
MONDO:0013267	distal 16p11.2 microdeletion syndrome
MONDO:0013260	esophagitis, eosinophilic, 2
MONDO:0013261	dilated cardiomyopathy 1R
MONDO:0013264	amyotrophic lateral sclerosis type 12
MONDO:0013265	autism, susceptibility to, 17
MONDO:0013262	dilated cardiomyopathy 1S
MONDO:0013263	retinitis pigmentosa 54
MONDO:0001268	gingival recession
MONDO:0001267	Lemierre syndrome
MONDO:0001266	erysipelas
MONDO:0001265	schizophreniform disorder
MONDO:0001269	scleral disease
MONDO:0001260	cercarial dermatitis
MONDO:0001264	Kyasanur forest disease
MONDO:0001263	histoplasmosis retinitis
MONDO:0001262	African histoplasmosis
MONDO:0001261	Mobitz type II atrioventricular block
MONDO:0013257	leprosy, susceptibility to, 6
MONDO:0013258	autism, susceptibility to, 16
MONDO:0013255	arthrogryposis, renal dysfunction, and cholestasis 2
MONDO:0013256	chromosome 15q24 deletion syndrome
MONDO:0013259	Oguchi disease-2
MONDO:0013250	autosomal recessive nonsyndromic deafness 85
MONDO:0013253	breast-ovarian cancer, familial, susceptibility to, 3
MONDO:0013254	microcephaly, seizures, and developmental delay
MONDO:0013251	Birbeck granule deficiency
MONDO:0013252	Warsaw breakage syndrome
MONDO:0001279	intraspinal meningioma
MONDO:0001278	adult respiratory distress syndrome
MONDO:0001277	cerebral arteritis
MONDO:0001276	expressive language disorder
MONDO:0001271	lens subluxation
MONDO:0001270	stone in bladder diverticulum
MONDO:0001275	spinal meningioma
MONDO:0001274	anal spasm
MONDO:0001273	megacolon
MONDO:0001272	functional diarrhea
MONDO:0013246	fatty liver disease, nonalcoholic, susceptibility to, 2
MONDO:0013247	Fanconi renotubular syndrome 2
MONDO:0013244	brachydactyly type E2
MONDO:0013245	syndromic multisystem autoimmune disease due to ITCH deficiency
MONDO:0013248	Fanconi anemia complementation group O
MONDO:0013249	autosomal recessive nonsyndromic deafness 84A
MONDO:0013242	maturity-onset diabetes of the young type 11
MONDO:0013243	neuronopathy, distal hereditary motor, type 2C
MONDO:0013240	maturity-onset diabetes of the young type 10
MONDO:0013241	spinocerebellar ataxia type 30
MONDO:0003700	brachial plexus neoplasm
MONDO:0003701	thyroid gland diffuse sclerosing papillary carcinoma
MONDO:0003702	uterus intravascular leiomyomatosis
MONDO:0003703	uterine corpus leiomyomatosis
MONDO:0003711	malignant peripheral nerve sheath tumor
MONDO:0003712	angiokeratoma of mibelli
MONDO:0003713	angiokeratoma circumscriptum
MONDO:0003714	bladder urachal squamous cell carcinoma
MONDO:0003710	ovarian mixed germ cell neoplasm
MONDO:0003708	extrahepatic bile duct small cell adenocarcinoma
MONDO:0003709	agoraphobia
MONDO:0003704	uterine corpus diffuse leiomyomatosis
MONDO:0003705	adult brainstem mixed glioma
MONDO:0003706	adult brainstem astrocytoma
MONDO:0003707	distal biliary tract carcinoma
MONDO:0003744	spindle cell intraocular melanoma
MONDO:0003745	choroid spindle cell melanoma
MONDO:0003746	ciliary body spindle cell melanoma
MONDO:0003747	telangiectatic glomangioma
MONDO:0003740	AIDS phobia
MONDO:0003741	juvenile type testicular granulosa cell tumor
MONDO:0003742	heart fibrosarcoma
MONDO:0003743	heart malignant hemangiopericytoma
MONDO:0015729	mosaic trisomy 16
MONDO:0015728	distal trisomy 15q
MONDO:0015727	mosaic trisomy 15
MONDO:0015733	low anorectal malformation
MONDO:0015732	intermediate anorectal malformation
MONDO:0015731	high anorectal malformation
MONDO:0015730	mosaic trisomy 17
MONDO:0015737	typical nemaline myopathy
MONDO:0015736	intermediate nemaline myopathy
MONDO:0015735	severe congenital nemaline myopathy
MONDO:0015734	rectal duplication
MONDO:0003737	malignant testicular Leydig cell tumor
MONDO:0003738	selective IgE deficiency disease
MONDO:0003739	selective immunoglobulin deficiency disease
MONDO:0003755	urinary tract non-invasive transitional cell neoplasm
MONDO:0003756	ovarian mucinous neoplasm
MONDO:0003757	paraplegia
MONDO:0003758	childhood testicular germ cell tumor
MONDO:0003751	childhood germ cell tumor
MONDO:0003752	frontal sinus Schneiderian papilloma
MONDO:0003753	nasal vestibule squamous papilloma
MONDO:0003754	Brown-Sequard syndrome
MONDO:0015719	severe hemophilia A
MONDO:0015718	mosaic trisomy 12
MONDO:0015717	mild hemophilia B
MONDO:0015716	moderately severe hemophilia B
MONDO:0003750	childhood central nervous system germ cell tumor
MONDO:0015722	congenital vitamin K-dependent coagulation factors deficiency
MONDO:0015721	mild hemophilia A
MONDO:0015720	moderately severe hemophilia A
MONDO:0015726	distal trisomy 14q
MONDO:0015725	mosaic trisomy 14
MONDO:0015724	non-distal trisomy 13q
MONDO:0015723	trisomy 12p
MONDO:0003748	flying phobia
MONDO:0003749	esophageal disease
MONDO:0003722	internal auditory canal meningioma
MONDO:0003723	blunt duct adenosis of breast
MONDO:0003724	non-proliferative fibrocystic change of the breast
MONDO:0003725	breast adenosis
MONDO:0003720	kidney fibrosarcoma
MONDO:0003721	kidney osteogenic sarcoma
MONDO:0015708	immuno-osseous dysplasia
MONDO:0015707	DNA repair defect other than combined T-cell and B-cell immunodeficiencies
MONDO:0015706	mosaic trisomy 1
MONDO:0015705	autosomal recessive centronuclear myopathy
MONDO:0015709	immunodeficiency syndrome with autoimmunity
MONDO:0015711	specific antibody deficiency with normal immunoglobulin concentrations and normal numbers of B cells
MONDO:0015710	immune dysregulation disease with immunodeficiency
MONDO:0015715	severe hemophilia B
MONDO:0015714	secondary central precocious puberty
MONDO:0015713	idiopathic central precocious puberty
MONDO:0015712	non-distal trisomy 10q
MONDO:0003719	renal pelvis neoplasm
MONDO:0003715	bladder urachal carcinoma
MONDO:0003716	renal pelvis papillary urothelial carcinoma
MONDO:0003717	renal pelvis papillary tumor
MONDO:0003718	occlusion precerebral artery
MONDO:0003733	central nervous system mature teratoma
MONDO:0003734	adult central nervous system immature teratoma
MONDO:0003735	central nervous system immature teratoma
MONDO:0003736	cancerophobia
MONDO:0003730	aleukemic leukemia
MONDO:0003731	adult central nervous system teratoma
MONDO:0003732	adult central nervous system mature teratoma
MONDO:0015700	immunodeficiency due to a late component of complement deficiency
MONDO:0015704	familial scaphocephaly syndrome
MONDO:0015703	T-B+ severe combined immunodeficiency due to CD3delta/CD3epsilon/CD3zeta
MONDO:0015702	T-B+ severe combined immunodeficiency due to CD45 deficiency
MONDO:0015701	T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiency
MONDO:0003726	apocrine adenosis of breast
MONDO:0003727	animal phobia
MONDO:0003728	breast fibrosarcoma
MONDO:0003729	aleukemic leukemia cutis
MONDO:0013190	factor XIII, b subunit, deficiency of
MONDO:0013191	focal segmental glomerulosclerosis 5
MONDO:0013194	Pseudopili annulati
MONDO:0013195	hypertrophic cardiomyopathy 13
MONDO:0013192	spondyloarthropathy, susceptibility to, 3
MONDO:0013193	thyrotoxic periodic paralysis, susceptibility to, 2
MONDO:0013198	dilated cardiomyopathy 1EE
MONDO:0013199	tuberous sclerosis 2
MONDO:0013196	colorectal cancer, hereditary nonpolyposis, type 8
MONDO:0013197	hypertrophic cardiomyopathy 14
MONDO:0013180	asthma-related traits, susceptibility to, 8
MONDO:0025163	white heifer disease
MONDO:0025167	reticuloendotheliosis, avian
MONDO:0013189	trichotillomania
MONDO:0013183	congenital stationary night blindness 1C
MONDO:0013184	congenital diarrhea 5 with tufting enteropathy
MONDO:0013181	amelogenesis imperfecta hypomaturation type 2A3
MONDO:0013182	chromosome 17p13.3 duplication syndrome
MONDO:0013187	factor XIII, A subunit, deficiency of
MONDO:0013188	cerebellar ataxia, intellectual disability, and dysequilibrium syndrome 3
MONDO:0013185	leprosy, susceptibility to, 5
MONDO:0013186	Noonan syndrome 6
MONDO:0001189	esophageal carcinoma
MONDO:0001188	esophagus lymphoma
MONDO:0025159	pneumonia of swine, mycoplasmal
MONDO:0001183	contact lens corneal edema
MONDO:0001182	idiopathic corneal edema
MONDO:0025152	non-human ape disease
MONDO:0001181	secondary corneal edema
MONDO:0001180	bullous keratopathy
MONDO:0001187	urinary bladder cancer
MONDO:0001186	depersonalization disorder
MONDO:0001185	dissociative amnesia
MONDO:0001184	chronic rapidly progressive glomerulonephritis
MONDO:0025155	hemorrhagic syndrome, bovine
MONDO:0013178	congenital muscular dystrophy due to LMNA mutation
MONDO:0013179	hereditary spastic paraplegia 44
MONDO:0013172	polymicrogyria with optic nerve hypoplasia
MONDO:0013173	intellectual disability, autosomal recessive 13
MONDO:0013170	cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies
MONDO:0013171	purine nucleoside phosphorylase deficiency
MONDO:0013176	ichthyosis-short stature-brachydactyly-microspherophakia syndrome
MONDO:0013177	congenital muscular dystrophy due to integrin alpha-7 deficiency
MONDO:0013174	primary ciliary dyskinesia 13
MONDO:0013175	retinitis pigmentosa 50
MONDO:0025149	encephalopathy, bovine spongiform
MONDO:0001199	dislocation of ear ossicle
MONDO:0001194	rickettsialpox
MONDO:0001193	chorioretinal scar
MONDO:0001192	esophageal melanoma
MONDO:0001191	hirudiniasis
MONDO:0001198	acquired thrombocytopenia
MONDO:0001197	qualitative platelet defect
MONDO:0001196	psychologic dyspareunia
MONDO:0001195	spotted fever
MONDO:0013169	chromosome 5p13 duplication syndrome
MONDO:0013167	parkinson disease 16
MONDO:0013168	dilated cardiomyopathy 1DD
MONDO:0001190	Brucella suis brucellosis
MONDO:0013161	autosomal recessive limb-girdle muscular dystrophy type 2O
MONDO:0013162	autosomal recessive limb-girdle muscular dystrophy type 2N
MONDO:0013160	muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B2
MONDO:0013165	hereditary spastic paraplegia 45
MONDO:0013166	GABA aminotransferase deficiency
MONDO:0013163	nephronophthisis-like nephropathy 1
MONDO:0013164	beta-ureidopropionase deficiency
MONDO:0025193	oculopharyngodistal myopathy
MONDO:0040797	vascular headache
MONDO:0003788	childhood embryonal testis carcinoma
MONDO:0001125	acute gonococcal epididymo-orchitis
MONDO:0003789	hereditary papillary renal cell carcinoma
MONDO:0001124	filariasis
MONDO:0001123	chronic sphenoidal sinusitis
MONDO:0001122	chronic maxillary sinusitis
MONDO:0003784	nasal cavity carcinoma in situ
MONDO:0001129	nasal cavity olfactory neuroblastoma
MONDO:0003785	leukopenia
MONDO:0001128	nasal cavity cancer
MONDO:0003786	childhood testicular choriocarcinoma
MONDO:0001127	tibialis tendinitis
MONDO:0003787	childhood testicular mixed germ cell cancer
MONDO:0001126	gastric ulcer
MONDO:0003780	T-cell immunodeficiency
MONDO:0003781	bronchitis
MONDO:0003782	uterine corpus epithelioid leiomyosarcoma
MONDO:0013109	leukemia, acute lymphocytic, susceptibility to, 2
MONDO:0003783	lymphopenia
MONDO:0001121	frontal sinusitis
MONDO:0027751	serpinopathy with loss of serpin function
MONDO:0001120	chronic frontal sinusitis
MONDO:0027750	serpinopathy with toxic serpin polymerization
MONDO:0015777	adult hypothyroidism
MONDO:0013114	autosomal dominant nonsyndromic deafness 50
MONDO:0013115	RIN2 syndrome
MONDO:0015776	rhizomelic chondrodysplasia punctata
MONDO:0013112	bronchiectasis with or without elevated sweat chloride 3
MONDO:0015775	non-rhizomelic chondrodysplasia punctata
MONDO:0013113	metaphyseal anadysplasia 2
MONDO:0015774	thoraco-abdominal enteric duplication
MONDO:0013118	Nijmegen breakage syndrome-like disorder
MONDO:0013119	autosomal recessive nonsyndromic deafness 77
MONDO:0015779	45,X/46,XY mixed gonadal dysgenesis
MONDO:0013116	congenital cataract-progressive muscular hypotonia-hearing loss-developmental delay syndrome
MONDO:0013117	progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 5
MONDO:0015778	syndromic hypothyroidism
MONDO:0040728	Campylobacter fetus infectious disease
MONDO:0001119	premature menopause
MONDO:0015773	fibular dimelia-diplopodia syndrome
MONDO:0013110	neurodegenerative syndrome due to cerebral folate transport deficiency
MONDO:0013111	acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins
MONDO:0015772	trisomy 8q
MONDO:0015771	mosaic trisomy 7
MONDO:0015770	congenital hypogonadotropic hypogonadism
MONDO:0001136	chylocele of tunica vaginalis
MONDO:0003799	conjunctivitis
MONDO:0001135	voyeurism
MONDO:0001134	essential hypertension
MONDO:0001133	malignant essential hypertension
MONDO:0003795	ovarian small cell carcinoma
MONDO:0027749	serpinopathy
MONDO:0001139	sexual masochism disorder
MONDO:0003796	rectum Kaposi sarcoma
MONDO:0001138	angiodysplasia of intestine
MONDO:0003797	inflammatory MFH
MONDO:0001137	Murray valley encephalitis
MONDO:0003798	epithelioid sarcoma
MONDO:0003791	prostatic urethral cancer
MONDO:0003792	ovarian carcinosarcoma
MONDO:0003793	uterine carcinosarcoma
MONDO:0003794	mediastinal neurilemmoma
MONDO:0001132	sexual sadism disorder
MONDO:0001131	duodenum adenocarcinoma
MONDO:0001130	nasal cavity lymphoma
MONDO:0003790	prostatic urethra urothelial carcinoma
MONDO:0015766	cholera
MONDO:0013103	epilepsy, idiopathic generalized, susceptibility to, 10
MONDO:0015765	congenital myopathy with cores
MONDO:0040732	Pseudomonas aeruginosa infectious disease
MONDO:0013104	basal cell carcinoma, susceptibility to, 4
MONDO:0015764	mosaic trisomy 20
MONDO:0013101	basal cell carcinoma, susceptibility to, 2
MONDO:0015763	mosaic trisomy 2
MONDO:0013102	basal cell carcinoma, susceptibility to, 3
MONDO:0013107	atopic dermatitis 7
MONDO:0013108	leukemia, acute lymphocytic, susceptibility to, 1
MONDO:0015769	distal trisomy 6p
MONDO:0015768	trisomy 5p
MONDO:0013105	basal cell carcinoma, susceptibility to, 5
MONDO:0015767	trisomy 4p
MONDO:0013106	basal cell carcinoma, susceptibility to, 6
MONDO:0015762	progressive familial intrahepatic cholestasis
MONDO:0015761	trisomy 10p
MONDO:0013100	atrial fibrillation, familial, 8
MONDO:0015760	T-cell non-Hodgkin lymphoma
MONDO:0001103	giardiasis
MONDO:0003766	thalamic cancer
MONDO:0001102	chronic endophthalmitis
MONDO:0003767	mitral valve disease
MONDO:0003768	signet ring cell variant cervical mucinous adenocarcinoma
MONDO:0001101	fat necrosis of breast
MONDO:0001100	hypertrophy of breast
MONDO:0003769	herpetic gastritis
MONDO:0003762	malignant leptomeningeal tumor
MONDO:0001107	cerebral lipidosis
MONDO:0001106	kidney failure
MONDO:0003763	acute stress disorder
MONDO:0001105	renal hypertension
MONDO:0003764	pediatric leptomeningeal melanoma
MONDO:0003765	adult leptomeningeal melanoma
MONDO:0001104	toxic diffuse goiter
MONDO:0003760	pediatric ovarian germ cell tumor
MONDO:0015749	6q16 deletion syndrome
MONDO:0003761	leptomeningeal melanoma
MONDO:0015755	myopathy with hexagonally cross-linked tubular arrays
MONDO:0015754	cylindrical spirals myopathy
MONDO:0015753	cap myopathy
MONDO:0037105	lung germ cell tumor
MONDO:0015752	intellectual disability-cataracts-kyphosis syndrome
MONDO:0015759	B-cell non-Hodgkin lymphoma
MONDO:0015758	primary cutaneous T-cell lymphoma
MONDO:0015757	lymphoid hemopathy
MONDO:0015756	myeloid hemopathy
MONDO:0003759	childhood ovarian yolk sac tumor
MONDO:0015751	craniosynostosis-hydrocephalus-Arnold-Chiari malformation type I-radioulnar synostosis syndrome
MONDO:0015750	amelogenesis imperfecta-gingival hyperplasia syndrome
MONDO:0001114	bacterial myocarditis
MONDO:0003777	renal pelvis urothelial papilloma
MONDO:0003778	primary immunodeficiency disease
MONDO:0001113	Fiedler's myocarditis
MONDO:0003779	gliomatosis cerebri
MONDO:0001112	bubonic plague
MONDO:0001111	thrombotic thrombocytopenic purpura
MONDO:0001118	Queensland tick typhus
MONDO:0003773	intracerebral cystic meningioma
MONDO:0003774	cerebral convexity meningioma
MONDO:0001117	methemoglobinemia
MONDO:0003775	lateral ventricle meningioma
MONDO:0001116	mesenteric lymphadenitis
MONDO:0003776	renal pelvis inverted papilloma
MONDO:0001115	familial polycythemia
MONDO:0003770	thoracic spinal canal and spinal cord meningioma
MONDO:0003771	jugular foramen meningioma
MONDO:0015739	adult-onset nemaline myopathy
MONDO:0003772	cerebral meningioma
MONDO:0015738	childhood-onset nemaline myopathy
MONDO:0001110	chronic pyelonephritis
MONDO:0015744	distal trisomy 19q
MONDO:0015743	idiopathic bilateral vestibulopathy
MONDO:0015742	periventricular leukomalacia
MONDO:0040753	inactive tuberculosis
MONDO:0015741	distal trisomy 18q
MONDO:0015748	hereditary mucosal leukokeratosis
MONDO:0015747	Amish infantile epilepsy syndrome
MONDO:0015746	male infertility due to globozoospermia
MONDO:0015745	microcephaly-polymicrogyria-corpus callosum agenesis syndrome
MONDO:0001109	petrositis
MONDO:0001108	broad ligament malignant neoplasm
MONDO:0015740	trisomy 18p
MONDO:0025136	tuberculosis, bovine
MONDO:0001169	spastic monoplegia
MONDO:0001168	spastic hemiplegia
MONDO:0025135	tuberculosis, avian
MONDO:0001167	spastic diplegia
MONDO:0025138	vesicular exanthema of swine
MONDO:0001166	nephritis
MONDO:0025139	white muscle disease
MONDO:0001161	schizoid personality disorder
MONDO:0001160	dissociative disorder
MONDO:0025130	swine vesicular disease
MONDO:0001165	tongue disease
MONDO:0001164	antisocial personality disorder
MONDO:0001163	paranoid personality disorder
MONDO:0001162	impulse control disorder
MONDO:0013158	muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A6
MONDO:0013159	muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B1
MONDO:0013156	muscular dystrophy-dystroglycanopathy (congenital without intellectual disability), type B4
MONDO:0013157	muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A5
MONDO:0013150	parkinsonism-dystonia, infantile
MONDO:0013151	choroidal dystrophy, central areolar, 3
MONDO:0013154	muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A2
MONDO:0013155	muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B3
MONDO:0013152	systemic lupus erythematosus, susceptibility to, 14
MONDO:0013153	inflammatory bowel disease 28
MONDO:0001179	pinguecula
MONDO:0001178	pseudopterygium
MONDO:0001177	anorectal stricture
MONDO:0025129	swine erysipelas
MONDO:0001172	salpingo-oophoritis
MONDO:0001171	acute salpingo-oophoritis
MONDO:0001170	hemiplegia
MONDO:0001176	lens disease
MONDO:0001175	immature cataract
MONDO:0001174	conjunctival vascular disease
MONDO:0001173	acute salpingitis
MONDO:0013147	dilated cardiomyopathy 1CC
MONDO:0013148	Brugada syndrome 8
MONDO:0013145	Brugada syndrome 6
MONDO:0013146	Brugada syndrome 7
MONDO:0013149	hydrops fetalis, nonimmune, with gracile bones and dysmorphic features
MONDO:0013140	candidiasis, familial, 4
MONDO:0013143	hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency
MONDO:0013144	antithrombin III deficiency
MONDO:0013141	autosomal dominant macrothrombocytopenia TUBB1-related
MONDO:0013142	neuropathy, hereditary sensory and autonomic, type 2B
MONDO:0001147	meningocele
MONDO:0025114	protozoan infections, animal
MONDO:0001146	fourth cranial nerve palsy
MONDO:0025113	poultry disease
MONDO:0001145	total third-nerve palsy
MONDO:0001144	partial third-nerve palsy
MONDO:0001149	microcephaly
MONDO:0001148	iliac vein thrombophlebitis
MONDO:0001143	paralytic strabismus
MONDO:0001142	salivary gland disease
MONDO:0001141	middle ear cholesterol granuloma
MONDO:0027772	lung colloid adenocarcinoma
MONDO:0001140	Edwards syndrome
MONDO:0040700	orbital dermoid cyst
MONDO:0015799	Smith-McCort dysplasia
MONDO:0013136	hereditary hypotrichosis with recurrent skin vesicles
MONDO:0013137	choroidal dystrophy, central areolar 2
MONDO:0015798	inflammatory myofibroblastic tumor
MONDO:0013134	glaucoma 1, open angle, O
MONDO:0015797	UV-sensitive syndrome
MONDO:0015796	acute lung injury
MONDO:0013135	familial hemophagocytic lymphohistiocytosis 5
MONDO:0013138	vertigo, benign recurrent, 2
MONDO:0013139	neutropenia, severe congenital, 2, autosomal dominant
MONDO:0015791	peripheral precocious puberty
MONDO:0015790	central diabetes insipidus
MONDO:0015795	undifferentiated embryonal sarcoma of the liver
MONDO:0013132	hereditary spastic paraplegia 36
MONDO:0015794	antenatal multiminicore disease with arthrogryposis multiplex congenita
MONDO:0013133	melanoma, cutaneous malignant, susceptibility to, 5
MONDO:0013130	isolated microphthalmia 4
MONDO:0015793	moderate multiminicore disease with hand involvement
MONDO:0013131	polycystic kidney disease 2
MONDO:0015792	transient congenital hypothyroidism
MONDO:0001158	obsessive-compulsive personality disorder
MONDO:0027766	generalized lipodystrophy
MONDO:0025102	monkey disease
MONDO:0027767	partial lipodystrophy
MONDO:0001157	dependent personality disorder
MONDO:0001156	borderline personality disorder
MONDO:0001155	gastrojejunal ulcer
MONDO:0001159	multiple personality disorder
MONDO:0001150	hydrocephalus
MONDO:0001154	Siberian tick typhus
MONDO:0001153	gender dysphoria
MONDO:0001152	amnestic disorder
MONDO:0025100	mastitis, bovine
MONDO:0001151	benign essential hypertension
MONDO:0013125	CLAPO syndrome
MONDO:0015788	symptomatic form of hemophilia B in female carriers
MONDO:0015787	symptomatic form of hemophilia A in female carriers
MONDO:0013126	Bartter syndrome, type 4B
MONDO:0013123	atrial septal defect 6
MONDO:0015786	Prader-Willi syndrome due to imprinting mutation
MONDO:0013124	pelvic organ prolapse, susceptibility to, 2
MONDO:0015785	Prader-Willi syndrome due to translocation
MONDO:0013129	cone dystrophy 4
MONDO:0013127	asphyxiating thoracic dystrophy 3
MONDO:0013128	familial juvenile hyperuricemic nephropathy type 2
MONDO:0015789	non-acquired combined pituitary hormone deficiencies without extra-pituitary malformations
MONDO:0015780	dyskeratosis congenita
MONDO:0013121	glaucoma 3, primary congenital, C
MONDO:0015784	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2
MONDO:0013122	glaucoma 3, primary congenital, D
MONDO:0015783	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1
MONDO:0015782	dysmorphism-cleft palate-loose skin syndrome
MONDO:0013120	46,XY sex reversal 5
MONDO:0015781	facial dysmorphism-shawl scrotum-joint laxity syndrome
MONDO:0003623	pancreatic acinar cell adenocarcinoma
MONDO:0003624	acinic cell breast carcinoma
MONDO:0003626	uterine ligament serous adenocarcinoma
MONDO:0003620	peripheral nervous system disease
MONDO:0003621	small intestinal vasoactive intestinal peptide producing tumor
MONDO:0003622	pancreatic vasoactive intestinal peptide producing tumor
MONDO:0015609	advanced sleep phase syndrome
MONDO:0015608	acute myeloid leukemia and myelodysplastic syndromes related to radiation
MONDO:0015607	partial chromosome Y deletion
MONDO:0015606	Xp22.3 microdeletion syndrome
MONDO:0015612	Dent disease
MONDO:0015611	neutral lipid storage disease
MONDO:0015610	acquired aplastic anemia
MONDO:0015616	rare genetic intestinal disease
MONDO:0015615	rare genetic gastroenterological disease
MONDO:0015614	dermatitis herpetiformis
MONDO:0015613	dentin dysplasia
MONDO:0003616	salpingitis isthmica nodosa
MONDO:0003617	chronic salpingitis
MONDO:0003618	pyosalpinx
MONDO:0003619	salpingitis
MONDO:0003634	proteinuria
MONDO:0003635	sebaceous breast carcinoma
MONDO:0003636	vulvar sebaceous carcinoma
MONDO:0003637	clear cell-sugar-tumor of the lung
MONDO:0003630	pancreatic serous cystadenocarcinoma
MONDO:0003631	cervical serous adenocarcinoma
MONDO:0003632	endocervicitis
MONDO:0003633	malignant mesenchymoma
MONDO:0015601	X-linked intellectual disability, van Esch type
MONDO:0015600	X-linked intellectual disability, Cilliers type
MONDO:0015605	distal monosomy 9p
MONDO:0015604	middle ear anomaly
MONDO:0015603	rare odontal or periodontal disorder
MONDO:0015602	developmental delay-deafness syndrome, Hildebrand type
MONDO:0003627	rheumatic pulmonary valve disease
MONDO:0003628	pulmonary valve disease
MONDO:0003629	uterine corpus serous adenocarcinoma
MONDO:0003601	mediastinum liposarcoma
MONDO:0003602	intracranial liposarcoma
MONDO:0003603	non-functioning pituitary gland neoplasm
MONDO:0003604	functioning pituitary gland neoplasm
MONDO:0003600	cutaneous liposarcoma
MONDO:0003612	uterine ligament cancer
MONDO:0003613	diffuse peritoneal leiomyomatosis
MONDO:0003614	intravenous leiomyomatosis
MONDO:0003615	nerve compression syndrome
MONDO:0003610	rete ovarii cystadenoma
MONDO:0003611	uterine ligament papillary cystadenoma associated with von Hippel-Lindau disease
MONDO:0003609	seminal vesicle cystadenoma
MONDO:0003605	adrenal neuroblastoma
MONDO:0003606	adrenal medulla cancer
MONDO:0003607	neuritis of upper limb
MONDO:0003608	optic atrophy
MONDO:0001089	acute inferolateral myocardial infarction
MONDO:0013070	spermatogenic failure 7
MONDO:0001084	primary optic atrophy
MONDO:0001083	Fanconi renotubular syndrome
MONDO:0001082	lymph node cancer
MONDO:0001081	acute cervicitis
MONDO:0001088	acute inferoposterior infarction
MONDO:0001087	schizotypal personality disorder
MONDO:0001086	partial optic atrophy
MONDO:0001085	interstitial nephritis
MONDO:0013079	primary biliary cholangitis 2
MONDO:0001080	acute gonococcal cervicitis
MONDO:0013073	palmoplantar keratoderma, nonepidermolytic, focal 1
MONDO:0013074	encephalocraniocutaneous lipomatosis
MONDO:0013071	Emery-Dreifuss muscular dystrophy 4, autosomal dominant
MONDO:0013072	Emery-Dreifuss muscular dystrophy 5, autosomal dominant
MONDO:0013077	Santos syndrome
MONDO:0013078	type 1 diabetes mellitus 24
MONDO:0013075	herpes simplex encephalitis, susceptibility to, 2
MONDO:0013076	attention deficit-hyperactivity disorder, susceptibility to, 7
MONDO:0001095	mediastinum neuroblastoma
MONDO:0001094	residual stage of open angle glaucoma
MONDO:0001093	colonic lymphangioma
MONDO:0001092	colon leiomyoma
MONDO:0001099	lactocele
MONDO:0001098	separation anxiety disorder
MONDO:0001097	juvenile glaucoma
MONDO:0001096	mediastinum ganglioneuroblastoma
MONDO:0040699	necrotizing scleritis
MONDO:0013068	age-related hearing impairment 2
MONDO:0040698	subacute bursitis
MONDO:0013069	autosomal recessive optic atrophy, OPA7 type
MONDO:0001091	lipoma of colon
MONDO:0001090	acute anterolateral myocardial infarction
MONDO:0013062	long QT syndrome 12
MONDO:0013063	ventricular fibrillation, paroxysmal familial, 2
MONDO:0013060	autosomal recessive Parkinson disease 14
MONDO:0013061	myofibrillar myopathy 6
MONDO:0013066	46,XY sex reversal 3
MONDO:0013067	cataract 34 multiple types
MONDO:0013064	multiple synostoses syndrome 3
MONDO:0013065	premature ovarian failure 7
MONDO:0001069	leukodystrophy
MONDO:0001068	osteomalacia
MONDO:0001067	early yaws
MONDO:0001062	pyloric antrum cancer
MONDO:0001061	pylorus cancer
MONDO:0001060	microinvasive gastric cancer
MONDO:0025030	digital dermatitis in cattle
MONDO:0001066	late yaws
MONDO:0001065	supine hypotensive syndrome
MONDO:0001064	acute eustachian salpingitis
MONDO:0027694	amyotrophic lateral sclerosis type 23
MONDO:0001063	cardia cancer
MONDO:0013059	Aicardi-Goutieres syndrome 5
MONDO:0013057	psoriasis 12, susceptibility to
MONDO:0013058	cystic leukoencephalopathy without megalencephaly
MONDO:0013051	autosomal recessive cutis laxa type 2B
MONDO:0013052	retinitis pigmentosa 42
MONDO:0013050	lethal polymalformative syndrome, Boissel type
MONDO:0013055	Stargardt macular degeneration, absent or hypoplastic corpus callosum, intellectual disability, and dysmorphic features
MONDO:0013056	developmental and epileptic encephalopathy, 39
MONDO:0013053	microcephaly-facio-cardio-skeletal syndrome, Hadziselimovic type
MONDO:0013054	microcephaly, growth retardation, cataract, hearing loss, and unusual appearance
MONDO:0001079	pancreatic steatorrhea
MONDO:0025028	vesicular stomatitis
MONDO:0001078	tropical sprue
MONDO:0001073	idiopathic progressive polyneuropathy
MONDO:0001072	mild pre-eclampsia
MONDO:0001071	intellectual disability
MONDO:0001070	adrenoleukodystrophy
MONDO:0001077	short bowel syndrome
MONDO:0001076	glucose intolerance
MONDO:0001075	steatorrhea
MONDO:0001074	chronic tic disorder
MONDO:0013048	hereditary spastic paraplegia 50
MONDO:0013049	DPM3-CDG
MONDO:0013046	glycogen storage disease due to muscle beta-enolase deficiency
MONDO:0013047	glycogen storage disease due to lactate dehydrogenase M-subunit deficiency
MONDO:0013040	atypical hemolytic-uremic syndrome with MCP/CD46 anomaly
MONDO:0013041	atypical hemolytic-uremic syndrome with I factor anomaly
MONDO:0013044	atypical hemolytic-uremic syndrome with thrombomodulin anomaly
MONDO:0013045	mycobacterium tuberculosis, susceptibility to, 3
MONDO:0013042	atypical hemolytic-uremic syndrome with B factor anomaly
MONDO:0013043	atypical hemolytic-uremic syndrome with C3 anomaly
MONDO:0025095	malaria, avian
MONDO:0025096	malignant catarrh
MONDO:0037002	benign phyllodes tumor
MONDO:0037003	malignant phyllodes tumor
MONDO:0025086	hip dysplasia, canine
MONDO:0025085	hepatitis, viral, animal
MONDO:0025087	classical swine fever
MONDO:0025089	infectious bovine rhinotracheitis
MONDO:0040654	autosomal dominant oculocutaneous albinism
MONDO:0040653	autosomal recessive ocular albinism
MONDO:0025082	helminthiasis, animal
MONDO:0013091	glycogen storage disease IXc
MONDO:0013092	glioma susceptibility 2
MONDO:0013090	chromosome 19q13.11 deletion syndrome
MONDO:0040674	orgasm disorder
MONDO:0040673	malignant peritoneal germ cell tumor
MONDO:0040671	class V glucose-6-phosphate dehydrogenase deficiency
MONDO:0013095	glioma susceptibility 6
MONDO:0013096	glioma susceptibility 7
MONDO:0013093	glioma susceptibility 3
MONDO:0013094	glioma susceptibility 5
MONDO:0013099	combined pituitary hormone deficiencies, genetic form
MONDO:0013097	glioma susceptibility 8
MONDO:0013098	noise induced hearing loss
MONDO:0013080	primary biliary cholangitis 3
MONDO:0013081	lymphoproliferative syndrome 1
MONDO:0025062	encephalomyelitis, enzootic porcine
MONDO:0025061	edema disease of swine
MONDO:0025066	epidermitis, exudative, of swine
MONDO:0040678	infiltrating urothelial carcinoma
MONDO:0040677	invasive carcinoma
MONDO:0040676	great vessel cancer
MONDO:0040675	myofibroblastoma
MONDO:0040679	urothelial carcinoma
MONDO:0013084	neuroblastoma, susceptibility to, 4
MONDO:0013085	neuroblastoma, susceptibility to, 5
MONDO:0013082	Hirschsprung disease-ganglioneuroblastoma syndrome
MONDO:0013083	neuroblastoma, susceptibility to, 3
MONDO:0013088	follicular lymphoma, susceptibility to, 1
MONDO:0013089	schizophrenia 13
MONDO:0013086	neuroblastoma, susceptibility to, 6
MONDO:0013087	bronchiectasis with or without elevated sweat chloride 2
MONDO:0001004	slate pneumoconiosis
MONDO:0003667	spermatocytoma
MONDO:0003668	extragonadal seminoma
MONDO:0001003	pneumoconiosis due to talc
MONDO:0003669	testicular seminoma
MONDO:0001002	pulmonary siderosis
MONDO:0001001	baritosis
MONDO:0003663	uterine ligament endometrioid adenocarcinoma
MONDO:0001008	blepharophimosis
MONDO:0001007	chronic meningitis
MONDO:0003664	hemolytic anemia
MONDO:0003665	cervical endometrioid adenocarcinoma
MONDO:0001006	glaucomatous atrophy of optic disc
MONDO:0001005	kaolin pneumoconiosis
MONDO:0003666	fallopian tube endometrioid adenocarcinoma
MONDO:0003660	adult lymphoma
MONDO:0003661	breast lymphoma
MONDO:0003662	endometrioid ovary carcinoma
MONDO:0001000	mixed mineral dust pneumoconiosis
MONDO:0015656	metabolic disease with epilepsy
MONDO:0015655	cerebral malformation with epilepsy
MONDO:0015654	idiopathic or cryptogenic familial epilepsy syndrome with identified loci/genes
MONDO:0015653	monogenic epilepsy
MONDO:0015659	infectious disease with epilepsy
MONDO:0015658	cerebral diseases of vascular origin with epilepsy
MONDO:0015657	inflammatory and autoimmune disease with epilepsy
MONDO:0015652	chromosomal anomaly with epilepsy as a major feature
MONDO:0015651	neurocutaneous syndrome with epilepsy
MONDO:0015650	epilepsy syndrome
MONDO:0001015	eosinophilic meningitis
MONDO:0003678	silent myocardial infarction
MONDO:0001014	chronic leukemia
MONDO:0003679	anteroseptal myocardial infarction
MONDO:0001013	fibrosclerosis of breast
MONDO:0001012	breast fibroadenosis
MONDO:0003674	subendocardial myocardial infarction
MONDO:0001019	suppression amblyopia
MONDO:0003675	posterolateral myocardial infarction
MONDO:0001018	lymphoblastic leukemia
MONDO:0001017	epididymal adenocarcinoma
MONDO:0003676	inferolateral myocardial infarct
MONDO:0001016	epididymis cancer
MONDO:0003677	lateral myocardial infarction
MONDO:0003670	posteroinferior myocardial infarction
MONDO:0003671	septal myocardial infarction
MONDO:0003672	posterior myocardial infarction
MONDO:0015639	benign partial epilepsy with secondarily generalized seizures in infancy
MONDO:0003673	apical myocardial infarction
MONDO:0001011	breast cyst
MONDO:0001010	natural killer cell leukemia
MONDO:0015645	eating seizures
MONDO:0015644	audiogenic seizures
MONDO:0015643	photosensitive epilepsy
MONDO:0015642	benign partial infantile seizures
MONDO:0015649	micturation-induced seizures
MONDO:0015648	startle epilepsy
MONDO:0015647	thinking seizures
MONDO:0015646	orgasm-induced seizures
MONDO:0001009	solitary cyst of breast
MONDO:0015641	benign infantile focal epilepsy with midline spikes and wave during sleep
MONDO:0015640	benign infantile seizures associated with mild gastroenteritis
MONDO:0003645	cavernous hemangioma of face
MONDO:0003646	rectum neuroendocrine neoplasm
MONDO:0003647	atrophic flaccid tympanic membrane
MONDO:0003648	tympanic membrane disease
MONDO:0003641	central nervous system hematopoietic neoplasm
MONDO:0003642	oral submucous fibrosis
MONDO:0003643	giant hemangioma
MONDO:0003644	cavernous hemangioma of colon
MONDO:0015629	von Willebrand disease type 2B
MONDO:0003640	verruciform xanthoma of skin
MONDO:0015628	von Willebrand disease type 2A
MONDO:0015634	isolated osteopoikilosis
MONDO:0015633	Bazex syndrome
MONDO:0015632	FASTKD2-related infantile mitochondrial encephalomyopathy
MONDO:0015631	von Willebrand disease type 2N
MONDO:0015638	benign partial epilepsy of infancy with complex partial seizures
MONDO:0015637	benign non-familial infantile seizures
MONDO:0015636	dirofilariasis
MONDO:0015635	porokeratotic eccrine ostial and dermal duct nevus
MONDO:0015630	von Willebrand disease type 2M
MONDO:0003638	lung meningioma
MONDO:0003639	lung hilum neoplasm
MONDO:0003656	hemoglobinuria
MONDO:0003657	methotrexate-associated lymphoproliferation
MONDO:0003658	B-cell lymphoma, unclassifiable, with features intermediate between diffuse large b-cell lymphoma and classical Hodgkin lymphoma
MONDO:0003659	pediatric lymphoma
MONDO:0003652	acute urate nephropathy
MONDO:0003653	stork bite
MONDO:0003654	childhood parosteal osteosarcoma
MONDO:0003655	cerebral lymphoma
MONDO:0015619	non-syndromic urogenital tract malformation
MONDO:0015618	genetic pancreatic disease
MONDO:0003650	mixed hepatoblastoma
MONDO:0003651	macrotrabecular hepatoblastoma
MONDO:0015617	genetic gastro-esophageal disease
MONDO:0015623	cavitary myiasis
MONDO:0015622	wound myiasis
MONDO:0015621	rare abdominal surgical disease
MONDO:0015620	syndromic urogenital tract malformation
MONDO:0015627	multiple epiphyseal dysplasia due to collagen 9 anomaly
MONDO:0015626	Charcot-Marie-Tooth disease
MONDO:0015625	diazoxide-resistant diffuse hyperinsulinism
MONDO:0015624	diazoxide-sensitive diffuse hyperinsulinism
MONDO:0003649	esophageal neuroendocrine tumor
MONDO:0001048	orbital granuloma
MONDO:0001047	adrenal cortical hypofunction
MONDO:0027676	congenital anomalies of kidney and urinary tract 2
MONDO:0001046	imperforate anus
MONDO:0001045	intestinal atresia
MONDO:0001049	Dressler syndrome
MONDO:0001040	nasopharyngitis
MONDO:0001044	esophageal atresia
MONDO:0001043	diaphragm disease
MONDO:0001042	patellar tendinitis
MONDO:0025013	non-human primate disease
MONDO:0001041	dentin caries
MONDO:0013037	Giacheti syndrome
MONDO:0015699	immunodeficiency due to a classical component pathway complement deficiency
MONDO:0013038	CLOVES syndrome
MONDO:0013035	orofaciodigital syndrome XI
MONDO:0015698	transient hypogammaglobulinemia of infancy
MONDO:0013036	Zechi-Ceide syndrome
MONDO:0015697	immunoglobulin heavy chain deficiency
MONDO:0013039	3M syndrome 2
MONDO:0015692	refractory anemia with excess blasts in transformation
MONDO:0015691	hypereosinophilic syndrome
MONDO:0013030	dilated cardiomyopathy 1BB
MONDO:0015690	myeloid neoplasm associated with PDGFRB rearrangement
MONDO:0015696	Good syndrome
MONDO:0013033	cerebral palsy, spastic quadriplegic, 2
MONDO:0015695	combined immunodeficiency due to CRAC channel dysfunction
MONDO:0013034	keratosis palmoplantaris striata 2
MONDO:0013031	chromosome 5Q14.3 deletion syndrome, distal
MONDO:0015694	malignant melanoma of the mucosa
MONDO:0015693	composite lymphoma
MONDO:0013032	epilepsy, idiopathic generalized, susceptibility to, 8
MONDO:0001059	gastric lymphoma
MONDO:0001058	gastric fundus cancer
MONDO:0025003	goat disease
MONDO:0001057	malignant gastric granular cell tumor
MONDO:0001056	gastric cancer
MONDO:0001051	acute otitis externa
MONDO:0001050	malignant otitis externa
MONDO:0001055	conjunctival pterygium
MONDO:0001054	double pterygium
MONDO:0001053	acute infection of pinna
MONDO:0001052	chronic fungal otitis externa
MONDO:0015689	myeloid neoplasm associated with PDGFRA rearrangement
MONDO:0013026	subepithelial mucinous corneal dystrophy
MONDO:0013027	posterior amorphous corneal dystrophy
MONDO:0015688	myeloid/lymphoid neoplasms associated with eosinophilia and abnormality of PDGFRA, PDGFRB, FGFR1 or JAK2
MONDO:0013024	chronic thromboembolic pulmonary hypertension
MONDO:0015687	chronic eosinophilic leukemia
MONDO:0015686	primary peritoneal carcinoma
MONDO:0013025	chromosome 6q24-q25 deletion syndrome
MONDO:0013028	adenosine monophosphate deaminase deficiency
MONDO:0013029	cerebellar ataxia type 9
MONDO:0015681	childhood disintegrative disorder
MONDO:0015680	rare pervasive developmental disorder
MONDO:0015685	peritoneal cystic mesothelioma
MONDO:0013022	restless legs syndrome, susceptibility to, 7
MONDO:0015684	malignant peritoneal mesothelioma
MONDO:0013023	orofacial cleft 12
MONDO:0015683	primary malignant peritoneal tumor
MONDO:0013020	narcolepsy 5, susceptibility to
MONDO:0015682	primary peritoneal tumor
MONDO:0013021	sterile multifocal osteomyelitis with periostitis and pustulosis
MONDO:0003689	familial hemolytic anemia
MONDO:0001026	bacterial infectious disease
MONDO:0001025	seminal vesicle chronic gonorrhea
MONDO:0001024	pneumonic plague
MONDO:0001023	prolymphocytic leukemia
MONDO:0003685	retroperitoneal germ cell neoplasm
MONDO:0003686	apocrine sweat gland neoplasm
MONDO:0001029	Klippel-Feil syndrome
MONDO:0001028	acute pericementitis
MONDO:0003687	endocardium cancer
MONDO:0003688	well differentiated papillary mesothelioma
MONDO:0001027	gonococcal seminal vesiculitis
MONDO:0003681	myxoid chondrosarcoma
MONDO:0003682	localized chondrosarcoma
MONDO:0003684	clear cell chondrosarcoma
MONDO:0001022	disuse amblyopia
MONDO:0001021	ametropic amblyopia
MONDO:0001020	amblyopia
MONDO:0003680	periosteal chondrosarcoma
MONDO:0013015	Brugada syndrome 5
MONDO:0015678	dysplasia of head of femur, Meyer type
MONDO:0013016	leukocyte adhesion deficiency 3
MONDO:0015677	cardiac diverticulum
MONDO:0013013	question mark ears, isolated
MONDO:0015676	hyperandrogenism due to cortisone reductase deficiency
MONDO:0015675	distomatosis
MONDO:0013014	spondyloepimetaphyseal dysplasia, aggrecan type
MONDO:0013019	spondyloepimetaphyseal dysplasia, Pakistani type
MONDO:0013017	hypotrichosis 5
MONDO:0013018	keratosis follicularis spinulosa decalvans, autosomal dominant
MONDO:0015679	autosomal thrombocytopenia with normal platelets
MONDO:0015670	cardiomyopathy
MONDO:0013011	atrial septal defect 5
MONDO:0015674	late infantile neuronal ceroid lipofuscinosis
MONDO:0015673	rare cardiac tumor
MONDO:0013012	inflammatory bowel disease 27
MONDO:0015672	diprosopus
MONDO:0015671	diphtheria
MONDO:0013010	autosomal recessive nonsyndromic deafness 71
MONDO:0001037	ring corneal ulcer
MONDO:0001036	hypopyon
MONDO:0001035	hypopyon ulcer
MONDO:0001034	marginal corneal ulcer
MONDO:0003696	meningeal melanocytoma
MONDO:0003697	non-invasive verrucous carcinoma of the penis
MONDO:0003698	penis verrucous carcinoma
MONDO:0001039	tonsillitis
MONDO:0003699	phobic disorder
MONDO:0001038	perforated corneal ulcer
MONDO:0003692	adult malignant mesenchymoma
MONDO:0003693	clear cell cystadenofibroma
MONDO:0003694	ovarian clear cell cystadenofibroma
MONDO:0003695	ovarian clear cell adenofibroma
MONDO:0001033	mycotic corneal ulcer
MONDO:0001032	Mooren ulcer
MONDO:0003690	adult anaplastic ependymoma
MONDO:0001031	purulent acute otitis media
MONDO:0001030	keratoconus, stable condition
MONDO:0003691	childhood malignant mesenchymoma
MONDO:0013004	hypotonia, seizures, and precocious puberty
MONDO:0015667	acute myeloid leukemia by FAB classification
MONDO:0013005	EAST syndrome
MONDO:0015666	familial idiopathic dilatation of the right atrium
MONDO:0015665	scleromyxedema
MONDO:0013002	cone-rod dystrophy 9
MONDO:0013003	isolated congenital hypoglossia/aglossia
MONDO:0015664	idiopathic pulmonary artery dilatation
MONDO:0013008	combined immunodeficiency due to STIM1 deficiency
MONDO:0013009	Megarbane-Jalkh syndrome
MONDO:0013006	isolated growth hormone deficiency type IB
MONDO:0015669	rare disease with dentinogenesis imperfecta
MONDO:0015668	hereditary dentin defect
MONDO:0013007	combined immunodeficiency due to ORAI1 deficiency
MONDO:0013000	porphyria due to ALA dehydratase deficiency
MONDO:0015663	diencephalic syndrome
MONDO:0013001	synesthesia
MONDO:0015662	hemorrhagic disorder due to an acquired coagulation factor defect
MONDO:0015661	dextrocardia
MONDO:0015660	sporadic fetal brain disruption sequence
MONDO:0003502	ureter squamous cell carcinoma
MONDO:0003503	fallopian tube squamous cell carcinoma
MONDO:0003504	anal canal neuroendocrine neoplasm
MONDO:0003505	femoral cancer
MONDO:0003500	squamous cell bile duct carcinoma
MONDO:0003501	external ear squamous cell carcinoma
MONDO:0003513	gastric teratoma
MONDO:0003514	malignant teratoma
MONDO:0003515	fallopian tube teratoma
MONDO:0003516	adult teratoma
MONDO:0003510	malignant testicular germ cell tumor
MONDO:0003511	testicular germ cell cancer
MONDO:0003512	mediastinal mesenchymal tumor
MONDO:0003506	pulmonary artery choriocarcinoma
MONDO:0003507	choriocarcinoma of ovary
MONDO:0003508	choriocarcinoma of testis
MONDO:0003509	pineal region choriocarcinoma
MONDO:0040566	inherited glutathione metabolism disease
MONDO:0015599	atopic keratoconjunctivitis
MONDO:0015598	acrodermatitis continua suppurativa of Hallopeau
MONDO:0015593	limbic encephalitis with nCMAgs antibodies
MONDO:0015592	limbic encephalitis with LGI1 antibodies
MONDO:0015591	limbic encephalitis associated with antibodies to cell membrane antigens
MONDO:0015590	classic paraneoplastic limbic encephalitis
MONDO:0015597	pustulosis palmaris et plantaris
MONDO:0015596	non-herpetic acute limbic encephalitis
MONDO:0015595	posttransplant acute limbic encephalitis
MONDO:0015594	non-paraneoplastic limbic encephalitis
MONDO:0015589	paraneoplastic limbic encephalitis
MONDO:0015588	limbic encephalitis
MONDO:0015587	rolandic epilepsy-speech dyspraxia syndrome
MONDO:0015582	rare disorder related with pregnancy, childbirth and puerperium
MONDO:0015581	bile acid synthesis defect with cholestasis and malabsorption
MONDO:0015580	distal monosomy 7q36
MONDO:0015586	benign familial mesial temporal lobe epilepsy
MONDO:0015585	cryptogenic late-onset epileptic spasms
MONDO:0015584	febrile infection-related epilepsy syndrome
MONDO:0015583	2p21 microdeletion syndrome
MONDO:0003546	third cranial nerve disease
MONDO:0003547	histiocytic and dendritic cell cancer
MONDO:0003548	adenosquamous breast carcinoma
MONDO:0003549	adenosquamous bile duct carcinoma
MONDO:0003542	dental pulp calcification
MONDO:0003543	trigeminal nerve disease
MONDO:0003544	spinal cord cancer
MONDO:0003545	intradural extramedullary spinal canal neoplasm
MONDO:0003540	acute T cell leukemia
MONDO:0015529	paroxysmal Hemicrania
MONDO:0003541	adult acute lymphoblastic leukemia
MONDO:0015535	xanthoma disseminatum
MONDO:0015534	juvenile xanthogranuloma
MONDO:0015533	benign cephalic histiocytosis
MONDO:0015532	generalized eruptive histiocytosis
MONDO:0015539	progressive nodular histiocytosis
MONDO:0015538	indeterminate dendritic cell tumor
MONDO:0015537	necrobiotic xanthogranuloma
MONDO:0015536	papular xanthoma
MONDO:0003539	T-cell adult acute lymphocytic leukemia
MONDO:0015531	non-Langerhans cell histiocytosis
MONDO:0015530	trigeminal autonomic cephalalgia
MONDO:0003557	optic nerve sheath meningioma
MONDO:0003558	adenosquamous prostate carcinoma
MONDO:0003559	cervical adenosquamous carcinoma
MONDO:0003553	ampulla of vater adenosquamous carcinoma
MONDO:0003554	adenosquamous colon carcinoma
MONDO:0003555	Bartholin gland adenosquamous carcinoma
MONDO:0003556	endometrial adenosquamous carcinoma
MONDO:0003550	esophageal adenosquamous carcinoma
MONDO:0003551	thymic adenosquamous carcinoma
MONDO:0015519	congenital or early infantile CACH syndrome
MONDO:0015518	infantile bilateral striatal necrosis
MONDO:0003552	adenosquamous gallbladder carcinoma
MONDO:0015524	hyperplastic polyposis syndrome
MONDO:0015523	epithelioid hemangioendothelioma
MONDO:0015522	situs ambiguus
MONDO:0015521	juvenile or adult CACH syndrome
MONDO:0015528	congenital epulis
MONDO:0015526	cold-induced sweating syndrome
MONDO:0015525	congenital pseudoarthrosis of the limbs
MONDO:0015520	late infantile CACH syndrome
MONDO:0003524	gastric gastrin-producing neuroendocrine tumor
MONDO:0003525	pancreatic gastrin-producing neuroendocrine tumor
MONDO:0003526	lung giant cell carcinoma
MONDO:0003527	Ferguson-Smith tumor
MONDO:0003520	malignant acrospiroma
MONDO:0003521	VIPoma
MONDO:0003522	male orgasm disorder
MONDO:0003523	gastrin-producing neuroendocrine tumor
MONDO:0015509	genetic biliary tract disease
MONDO:0015508	genetic parenchymatous liver disease
MONDO:0015507	rare genetic hepatic disease
MONDO:0040502	glucocorticoid deficiency 5
MONDO:0015513	rare genetic endocrine disease
MONDO:0040501	ehlers-danlos syndrome, arthrochalasia type, 2
MONDO:0015512	genetic hypertension
MONDO:0040500	glycosylphosphatidylinositol biosynthesis defect 16
MONDO:0015511	rare genetic urogenital disease
MONDO:0015510	rare genetic respiratory disease
MONDO:0015517	common variable immunodeficiency
MONDO:0015516	symbrachydactyly of hands and feet
MONDO:0015515	carnitine palmitoyltransferase II deficiency
MONDO:0040503	blepharocheilodontic syndrome 2
MONDO:0015514	genetic endocrine growth disease
MONDO:0003517	mature teratoma
MONDO:0003518	mediastinum teratoma
MONDO:0003519	malignant syringoma
MONDO:0003535	fallopian tube papillary adenocarcinoma
MONDO:0003536	fallopian tube serous adenocarcinoma
MONDO:0003537	precursor T-lymphoblastic lymphoma/leukemia
MONDO:0003538	precursor lymphoblastic lymphoma/leukemia
MONDO:0003531	papillary eccrine carcinoma
MONDO:0003532	breast papillary carcinoma
MONDO:0003533	gastric papillary adenocarcinoma
MONDO:0003534	papillary thymic adenocarcinoma
MONDO:0003530	aggressive digital papillary adenocarcinoma
MONDO:0015502	pinnae and external auditory canal anomaly
MONDO:0015501	syndrome or malformation associated with head and neck malformations
MONDO:0015500	facial arteriovenous malformation
MONDO:0015506	rare syndrome with cardiac malformations
MONDO:0015505	tracheal anomaly
MONDO:0015504	larynx anomaly
MONDO:0015503	nose and cavum anomaly
MONDO:0003528	Volkmann contracture
MONDO:0003529	acute pyelonephritis
MONDO:0003586	esophagus liposarcoma
MONDO:0003587	pediatric liposarcoma
MONDO:0003588	larynx liposarcoma
MONDO:0003589	liposarcoma of the ovary
MONDO:0003582	hereditary breast ovarian cancer syndrome
MONDO:0003583	atypical lipomatous tumor
MONDO:0003584	visual cortex disease
MONDO:0003585	adult liposarcoma
MONDO:0003580	embryonal testis carcinoma
MONDO:0003581	ovarian embryonal carcinoma
MONDO:0015579	Hb Bart's hydrops fetalis
MONDO:0015578	rare mycosis
MONDO:0015577	rare parasitic disease
MONDO:0015576	rare viral disease
MONDO:0015571	deletion 5q35
MONDO:0015570	isolated congenital auditory ossicle malformation
MONDO:0015575	rare bacterial infectious disease
MONDO:0015574	chronic cutaneous lupus erythematosus
MONDO:0015573	subacute cutaneous lupus erythematosus
MONDO:0015572	cerebral malformation due to abnormal neuronal migration
MONDO:0003598	median nerve neuropathy
MONDO:0003599	vulvar liposarcoma
MONDO:0003593	breast liposarcoma
MONDO:0003594	mixed liposarcoma
MONDO:0003595	sclerosing liposarcoma
MONDO:0003596	spindle cell liposarcoma
MONDO:0003590	fibroblastic liposarcoma
MONDO:0003591	kidney liposarcoma
MONDO:0003592	gastric liposarcoma
MONDO:0015568	isolated congenital nasal pyriform aperture stenosis
MONDO:0015567	cataract-glaucoma syndrome
MONDO:0015566	2q24 microdeletion syndrome
MONDO:0015565	cap polyposis
MONDO:0015569	congenital nasal pyriform aperture stenosis with holoprosencephaly
MONDO:0015560	classic mast cell leukemia
MONDO:0015564	Castleman disease
MONDO:0015563	blue cone monochromatism
MONDO:0015562	distal monosomy 17q
MONDO:0015561	aleukemic mast cell leukemia
MONDO:0003568	disorder of optic chiasm
MONDO:0003569	cranial nerve neuropathy
MONDO:0003564	localized pulmonary fibrosis
MONDO:0003565	urethral villous adenoma
MONDO:0003566	choroid plexus carcinoma
MONDO:0003567	bilateral hypoactive labyrinth
MONDO:0003560	adenosquamous pancreas carcinoma
MONDO:0003561	malignant giant cell tumor of soft parts
MONDO:0003562	rete testis neoplasm
MONDO:0003563	diffuse pulmonary fibrosis
MONDO:0015557	Smouldering systemic mastocytosis
MONDO:0015556	nodular urticaria pigmentosa
MONDO:0015555	plaque-form urticaria pigmentosa
MONDO:0015554	typical urticaria pigmentosa
MONDO:0015559	lymphoadenopathic mastocytosis with eosinophilia
MONDO:0015558	isolated bone marrow mastocytosis
MONDO:0015553	dystrophic epidermolysis bullosa, nails only
MONDO:0015552	acral dystrophic epidermolysis bullosa
MONDO:0015551	basal epidermolysis bullosa simplex
MONDO:0015550	suprabasal epidermolysis bullosa simplex
MONDO:0003579	retinal nerve fibre layer disorder
MONDO:0003575	comedocarcinoma
MONDO:0003577	cribriform carcinoma
MONDO:0003578	extragonadal nonseminomatous germ cell tumor
MONDO:0003571	labyrinthine dysfunction
MONDO:0003572	nasopharyngeal type undifferentiated carcinoma
MONDO:0003573	pleomorphic carcinoma
MONDO:0003574	external ear cancer
MONDO:0003570	lipid-rich carcinoma
MONDO:0015546	non-distal monosomy 10q
MONDO:0015545	macrophage activation syndrome
MONDO:0015544	acquired hemophagocytic lymphohistiocytosis associated with malignant disease
MONDO:0015543	hemophagocytic syndrome associated with an infection
MONDO:0015549	rare genetic hematologic disease
MONDO:0015548	Huntington disease-like syndrome
MONDO:0015547	genetic dementia
MONDO:0015542	secondary hemophagocytic lymphohistiocytosis
MONDO:0015541	genetic hemophagocytic lymphohistiocytosis
MONDO:0015540	hemophagocytic syndrome
MONDO:0021251	endometrium neoplasm
MONDO:0021250	tonsil neoplasm
MONDO:0021259	prostate neoplasm
MONDO:0021258	choroid neoplasm
MONDO:0021257	glomus jugulare neoplasm
MONDO:0008279	familial adenomatous polyposis type 1
MONDO:0008277	stomach polyp
MONDO:0021254	corpus uteri neoplasm
MONDO:0008278	juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome
MONDO:0008275	familial expansile osteolysis
MONDO:0021253	gallbladder neoplasm
MONDO:0008276	generalized juvenile polyposis/juvenile polyposis coli
MONDO:0021252	lung hilum neoplasm
MONDO:0008273	actinic prurigo
MONDO:0008274	polyostotic fibrous dysplasia
MONDO:0008271	polydactyly of an index finger
MONDO:0008272	polysyndactyly 4
MONDO:0008270	polydactyly of a triphalangeal thumb
MONDO:0021249	lip neoplasm
MONDO:0021240	tongue neoplasm
MONDO:0021248	nervous system neoplasm
MONDO:0021247	renal pelvis neoplasm
MONDO:0021246	pharynx neoplasm
MONDO:0021245	oral cavity neoplasm
MONDO:0021244	submandibular gland neoplasm
MONDO:0008288	popliteal cyst
MONDO:0021243	parotid gland neoplasm
MONDO:0008289	brain small vessel disease 1 with or without ocular anomalies
MONDO:0008286	crossed polysyndactyly
MONDO:0021242	sublingual gland neoplasm
MONDO:0008287	Greig cephalopolysyndactyly syndrome
MONDO:0021241	buccal mucosa neoplasm
MONDO:0008284	polyposis of gastric fundus without polyposis coli
MONDO:0008285	polyps, multiple and recurrent inflammatory fibroid, gastrointestinal
MONDO:0008282	polyposis, intestinal, with multiple exostoses
MONDO:0008283	Cronkhite-Canada syndrome
MONDO:0008280	Peutz-Jeghers syndrome
MONDO:0008281	polyposis, intestinal, scattered and discrete
MONDO:0021239	urethra neoplasm
MONDO:0021238	cornea neoplasm
MONDO:0033259	deafness, autosomal dominant 72
MONDO:0033258	deafness, autosomal dominant 71
MONDO:0008259	familial spontaneous pneumothorax
MONDO:0021237	adrenal medulla neoplasm
MONDO:0021235	external ear neoplasm
MONDO:0008257	platelet responsiveness to adrenaline, depressed
MONDO:0021234	spinal cord neoplasm
MONDO:0008258	platelet signal processing defect
MONDO:0008255	platelet factor 3 deficiency
MONDO:0021233	ear neoplasm
MONDO:0008256	platelet membrane fluidity
MONDO:0021232	pineal body neoplasm
MONDO:0008253	platelet aggregation, spontaneous
MONDO:0021231	retina neoplasm
MONDO:0021230	uterine cervix neoplasm
MONDO:0008254	platelet disorder, undefined
MONDO:0008251	familial pityriasis rubra pilaris
MONDO:0033262	nephrotic syndrome 15
MONDO:0008252	platelet adenylate cyclase activity
MONDO:0033260	deafness, autosomal dominant 73
MONDO:0008250	isolated growth hormone deficiency type II
MONDO:0033261	deafness, autosomal dominant 34, with or without inflammation
MONDO:0021229	ciliary body neoplasm
MONDO:0021228	brainstem neoplasm
MONDO:0021227	adrenal gland neoplasm
MONDO:0011899	Noonan syndrome-like disorder with loose anagen hair
MONDO:0021225	uvea neoplasm
MONDO:0008268	polydactyly-myopia syndrome
MONDO:0021224	iris neoplasm
MONDO:0008269	polydactyly of a biphalangeal thumb
MONDO:0021223	digestive system neoplasm
MONDO:0021222	lacrimal gland neoplasm
MONDO:0008266	polydactyly, postaxial, type A1
MONDO:0008267	orofaciodigital syndrome V
MONDO:0021221	vestibulocochlear nerve neoplasm
MONDO:0021220	eye neoplasm
MONDO:0008264	autosomal dominant medullary cystic kidney disease with or without hyperuricemia
MONDO:0008265	polycystic liver disease 1
MONDO:0008262	Poland syndrome
MONDO:0008263	polycystic kidney disease 1
MONDO:0008260	Kindler syndrome
MONDO:0008261	hereditary sclerosing poikiloderma, Weary type
MONDO:0021218	placenta neoplasm
MONDO:0021294	carcinoma in situ of gastric cardia
MONDO:0021292	carcinoma in situ of gastric body
MONDO:0021291	carcinoma in situ of fundus of stomach
MONDO:0021290	carcinoma in situ of appendix
MONDO:0021299	carcinoma in situ of extrahepatic bile duct
MONDO:0021298	carcinoma in situ of oropharynx
MONDO:0021297	carcinoma in situ of nasopharynx
MONDO:0021296	carcinoma in situ of renal pelvis
MONDO:0033204	ciliary dyskinesia, primary, 37
MONDO:0033202	deafness, autosomal recessive 109
MONDO:0033203	nephrotic syndrome 14
MONDO:0033200	deafness, autosomal recessive 108
MONDO:0033201	deafness, autosomal recessive 57
MONDO:0021284	carcinoma in situ of ureter
MONDO:0021283	malignant teratoma of mediastinum
MONDO:0021282	malignant teratoma of testis
MONDO:0021281	cavernous hemangioma of retina
MONDO:0021280	mucoepidermoid carcinoma of parotid gland
MONDO:0021289	carcinoma in situ of cecum
MONDO:0021288	carcinoma in situ of hypopharynx
MONDO:0021287	carcinoma in situ of epiglottis
MONDO:0021285	carcinoma in situ of urethra
MONDO:0033211	diencephalic-mesencephalic junction dysplasia syndrome
MONDO:0021273	leiomyoma of ciliary body
MONDO:0021272	inherited orthostatic hypotension
MONDO:0021271	villous adenoma of colon
MONDO:0021279	mucoepidermoid carcinoma of submandibular gland
MONDO:0008299	posterior column ataxia
MONDO:0021276	papilloma of buccal mucosa
MONDO:0008297	variegate porphyria
MONDO:0021275	papilloma of eyelid
MONDO:0008298	postaxial tetramelic oligodactyly
MONDO:0008295	sporadic porphyria cutanea tarda
MONDO:0008296	familial porphyria cutanea tarda
MONDO:0008293	porokeratosis 3, disseminated superficial actinic type
MONDO:0008294	acute intermittent porphyria
MONDO:0008291	porokeratosis plantaris palmaris et disseminata
MONDO:0008292	punctate palmoplantar keratoderma type 2
MONDO:0008290	porokeratosis 1, Mibelli type
MONDO:0021260	sensory ganglionopathy
MONDO:0035892	Mills syndrome
MONDO:0023833	multifocal choroiditis
MONDO:0011845	migraine with or without aura, susceptibility to, 3
MONDO:0011844	myoclonic dystonia 15
MONDO:0011847	migraine without aura, susceptibility to, 4
MONDO:0011846	bulimia nervosa, susceptibility to, 1
MONDO:0011849	psoriatic arthritis
MONDO:0011848	headache associated with sexual activity
MONDO:0011850	migraine with or without aura, susceptibility to, 5
MONDO:0011852	nonsyndromic congenital nail disorder 8
MONDO:0011851	migraine with or without aura, susceptibility to, 6
MONDO:0011854	secretory diarrhea, myopathy, and deafness
MONDO:0011853	Camptosynpolydactyly, complex
MONDO:0008208	patella, familial recurrent dislocation of
MONDO:0008209	Char syndrome
MONDO:0023820	Moebius axonal neuropathy hypogonadism
MONDO:0008206	benign paroxysmal tonic upgaze of childhood with ataxia
MONDO:0008207	chondromalacia patellae
MONDO:0011834	spinocerebellar ataxia type 18
MONDO:0008204	patella aplasia, coxa vara, and tarsal synostosis
MONDO:0011833	spinocerebellar ataxia type 21
MONDO:0008205	patella aplasia/hypoplasia
MONDO:0011836	thyroid Hurthle cell carcinoma
MONDO:0008202	Parotidomegaly, hereditary bilateral
MONDO:0011835	sensory ataxic neuropathy, dysarthria, and ophthalmoparesis
MONDO:0008203	Passovoy factor defect
MONDO:0011838	Bothnia retinal dystrophy
MONDO:0008200	autosomal dominant Parkinson disease 1
MONDO:0008201	Perry syndrome
MONDO:0011837	vitamin K-dependent clotting factors, combined deficiency of, type 2
MONDO:0011839	Newfoundland cone-rod dystrophy
MONDO:0011841	biotin-responsive basal ganglia disease
MONDO:0011840	dilated cardiomyopathy 1M
MONDO:0011843	hypertrophic cardiomyopathy 25
MONDO:0011842	Grn-related frontotemporal lobar degeneration with Tdp43 inclusions
MONDO:0011823	developmental malformations-deafness-dystonia syndrome
MONDO:0011822	Bartter disease type 3
MONDO:0011825	streptococcus, group A, severity of infection by
MONDO:0011824	autism, susceptibility to, 8
MONDO:0011827	patent ductus arteriosus
MONDO:0011826	glucocorticoid deficiency 2
MONDO:0011829	coenzyme Q10 deficiency, primary, 1
MONDO:0011828	intellectual disability, autosomal recessive 2
MONDO:0023809	Milner-Khallouf-Gibson syndrome
MONDO:0011830	lissencephaly due to LIS1 mutation
MONDO:0011832	autosomal dominant nonsyndromic deafness 44
MONDO:0011831	arrhythmogenic right ventricular dysplasia 8
MONDO:0023807	midphalangeal hair
MONDO:0011819	spinocerebellar ataxia type 19/22
MONDO:0011812	Duane-radial ray syndrome
MONDO:0011811	autosomal recessive cerebellar ataxia-saccadic intrusion syndrome
MONDO:0011814	Smith-McCort dysplasia 1
MONDO:0011813	polydactyly, postaxial, type A3
MONDO:0011816	lathosterolosis
MONDO:0011815	hypertension, essential, susceptibility to, 3
MONDO:0011818	isolated focal cortical dysplasia type II
MONDO:0011817	coronary heart disease, susceptibility to, 1
MONDO:0011821	Meckel syndrome, type 3
MONDO:0011820	scoliosis, isolated, susceptibility to, 2
MONDO:0023873	Noonan-like/multiple giant cell lesion syndrome
MONDO:0008239	phosphoglucomutase 4
MONDO:0011889	Charcot-Marie-Tooth disease type 2I
MONDO:0008237	phocomelia-ectrodactyly-deafness-sinus arrhythmia syndrome
MONDO:0011888	immunodeficiency 67
MONDO:0008238	phosphatase, acid, of tissues
MONDO:0008235	pheochromocytoma-islet cell tumor syndrome
MONDO:0008236	phlebectasia of lips
MONDO:0008233	pheochromocytoma
MONDO:0021211	brain neoplasm
MONDO:0021210	trachea neoplasm
MONDO:0008234	multiple endocrine neoplasia type 2A
MONDO:0008231	Peyronie disease
MONDO:0008232	phagocytosis, plasma-related defect 1N
MONDO:0011892	epilepsy, idiopathic generalized, susceptibility to, 9
MONDO:0011891	febrile seizures, familial, 8
MONDO:0008230	peroxidase, salivary
MONDO:0011894	Charcot-Marie-Tooth disease type 2E
MONDO:0011893	autosomal dominant nonsyndromic deafness 52
MONDO:0021209	heart neoplasm
MONDO:0021208	endocrine alopecia
MONDO:0011896	Parkinson disease 11, autosomal dominant, susceptibility to
MONDO:0011895	idiopathic hypereosinophilic syndrome
MONDO:0021207	Crohn jejunitis
MONDO:0021206	chronic non-suppurative otitis media
MONDO:0011898	Charcot-Marie-Tooth disease, axonal, with vocal cord paresis, autosomal recessive
MONDO:0011897	leukoencephalopathy-ataxia-hypodontia-hypomyelination syndrome
MONDO:0021205	disease of ear
MONDO:0023868	melanoma associated retinopathy
MONDO:0011890	Charcot-Marie-Tooth disease type 1D
MONDO:0023865	corneal infection
MONDO:0011878	Worth syndrome
MONDO:0008248	pigmented purpuric eruption
MONDO:0021204	chronic otitis media
MONDO:0011877	autosomal dominant osteopetrosis 1
MONDO:0021203	serous otitis media
MONDO:0008249	pilonidal sinus
MONDO:0008246	pigmented paravenous retinochoroidal atrophy
MONDO:0021202	allergic otitis media
MONDO:0021201	skin infection
MONDO:0008247	robin sequence-oligodactyly syndrome
MONDO:0011879	neuronopathy, distal hereditary motor, type 7B
MONDO:0008244	piebaldism
MONDO:0021200	rare disease
MONDO:0008245	piebald trait-neurologic defects syndrome
MONDO:0008242	photomyoclonus, diabetes mellitus, deafness, nephropathy, and cerebral dysfunction
MONDO:0008243	Pick disease
MONDO:0011881	keratosis palmoplantaris striata 3
MONDO:0008240	6-phosphogluconolactonase deficiency
MONDO:0011880	candidiasis, familial, 3
MONDO:0008241	phosphoglycoprotein 1
MONDO:0011883	Curly hair - acral keratoderma - caries syndrome
MONDO:0011882	skin fragility-woolly hair-palmoplantar keratoderma syndrome
MONDO:0011885	tubulointerstitial nephritis and uveitis syndrome
MONDO:0011884	hypotrichosis-osteolysis-periodontitis-palmoplantar keratoderma syndrome
MONDO:0011887	cataract, congenital, with mental impairment and dentate gyrus atrophy
MONDO:0011886	torsion dystonia 13
MONDO:0008219	pemphigus vulgaris
MONDO:0008217	pelvis-shoulder dysplasia
MONDO:0008218	Hailey-Hailey disease
MONDO:0011867	microphthalmia with cyst, bilateral facial clefts, and limb anomalies
MONDO:0008215	adult-onset autosomal dominant demyelinating leukodystrophy
MONDO:0011866	pontocerebellar hypoplasia type 1A
MONDO:0008216	pelvic lipomatosis with crossed renal ectopia
MONDO:0008213	pectus excavatum
MONDO:0011869	epidermolysis bullosa simplex superficialis
MONDO:0008214	Pelger-Huet anomaly
MONDO:0011868	lethal congenital contracture syndrome 2
MONDO:0008211	pseudoleprechaunism syndrome, Patterson type
MONDO:0008212	Pechet factor deficiency
MONDO:0008210	patterned macular dystrophy 1
MONDO:0011870	annular epidermolytic ichthyosis
MONDO:0011872	Griscelli syndrome type 2
MONDO:0011871	Niemann-Pick disease type B
MONDO:0011874	neonatal ichthyosis-sclerosing cholangitis syndrome
MONDO:0011873	Niemann-Pick disease, type C2
MONDO:0011876	juvenile absence epilepsy
MONDO:0011875	epilepsy, idiopathic generalized, susceptibility to, 11
MONDO:0008228	pernicious anemia
MONDO:0008229	peroneal nerve, accessory deep
MONDO:0008226	periodontitis, aggressive 1
MONDO:0011856	spondylometaphyseal dysplasia-bowed forearms-facial dysmorphism syndrome
MONDO:0008227	peripheral dysostosis
MONDO:0011855	granular corneal dystrophy type II
MONDO:0008224	hyperkalemic periodic paralysis
MONDO:0011858	spastic paraplegia, ataxia, and intellectual disability
MONDO:0011857	atrial fibrillation, familial, 3
MONDO:0008225	normokalemic periodic paralysis
MONDO:0008222	Andersen-Tawil syndrome
MONDO:0008223	hypokalemic periodic paralysis
MONDO:0011859	distal myopathy with early respiratory muscle involvement
MONDO:0008220	pepsinogen 3, group 1
MONDO:0008221	prolidase deficiency
MONDO:0011861	breath-holding Spells
MONDO:0011860	leprosy, susceptibility to, 2
MONDO:0011863	prostate cancer aggressiveness quantitative trait locus on chromosome 19
MONDO:0011862	hereditary spastic paraplegia 24
MONDO:0011865	COL4A1-related familial vascular leukoencephalopathy
MONDO:0011864	immunodeficiency, common variable, 1
MONDO:0011929	chromosome 1p36 deletion syndrome
MONDO:0011922	nonimmune chronic idiopathic neutropenia of adults
MONDO:0011921	aural atresia, congenital
MONDO:0011924	panic disorder 2
MONDO:0011923	osteoarthritis susceptibility 3
MONDO:0011926	psoriasis 9, susceptibility to
MONDO:0011925	congenital merosin-deficient muscular dystrophy 1A
MONDO:0011928	caudal duplication
MONDO:0011927	tufted angioma
MONDO:0011931	ovarian cancer, susceptibility to, 1
MONDO:0011930	epilepsy, familial adult myoclonic, 2
MONDO:0011919	autoimmune disease, susceptibility to, 1
MONDO:0011918	anxiety
MONDO:0011911	craniolenticulosutural dysplasia
MONDO:0011910	autosomal dominant limb-girdle muscular dystrophy type 1C
MONDO:0011913	Alzheimer disease 3
MONDO:0011912	autosomal recessive nonsyndromic deafness 37
MONDO:0011915	mitral valve prolapse, myxomatous 2
MONDO:0011914	hypotrichosis-lymphedema-telangiectasia syndrome
MONDO:0011917	focal segmental glomerulosclerosis 3, susceptibility to
MONDO:0011916	Charcot-Marie-Tooth disease axonal type 2K
MONDO:0011920	autosomal dominant nonsyndromic deafness 48
MONDO:0011908	juvenile myelomonocytic leukemia
MONDO:0011907	acrocapitofemoral dysplasia
MONDO:0011909	Charcot-Marie-Tooth disease dominant intermediate D
MONDO:0011900	porokeratosis 4, disseminated superficial actinic type
MONDO:0011902	Charcot-Marie-Tooth disease type 1F
MONDO:0011901	Charcot-Marie-Tooth disease axonal type 2H
MONDO:0011904	seizures, benign familial infantile, 3
MONDO:0011903	Charcot-Marie-Tooth disease type 2J
MONDO:0011906	congenital bile acid synthesis defect 1
MONDO:0011905	familial hypercholanemia
MONDO:0033282	multiple mitochondrial dysfunctions syndrome 5
MONDO:0033280	nephrotic syndrome 16
MONDO:0033281	polycystic kidney disease 5
MONDO:0021130	disorder of sphingolipid biosynthesis
MONDO:0021138	bone marrow cancer
MONDO:0021137	not rare
MONDO:0008158	dacryocystitis-osteopoikilosis syndrome
MONDO:0060733	humerofemoral hypoplasia with radiotibial ray deficiency
MONDO:0021136	rare
MONDO:0008159	postmenopausal osteoporosis
MONDO:0060732	tetraamelia syndrome 2
MONDO:0021135	rare or common
MONDO:0008156	autosomal dominant osteopetrosis 2
MONDO:0021134	acquired factor X deficiency
MONDO:0008157	Buschke-Ollendorff syndrome
MONDO:0021133	acquired factor XIII deficiency
MONDO:0008154	osteomas of mandible
MONDO:0021132	tertiary hyperparathyroidism
MONDO:0021131	frontal lobe ependymal tumor
MONDO:0008155	osteomesopyknosis
MONDO:0008152	multicentric carpo-tarsal osteolysis with or without nephropathy
MONDO:0008153	progressive osseous heteroplasia
MONDO:0008150	osteoglophonic dwarfism
MONDO:0008151	gnathodiaphyseal dysplasia
MONDO:0021129	microphthalmia
MONDO:0021128	has an isolated presentation
MONDO:0033123	exudative vitreoretinopathy 7
MONDO:0060729	protoporphyria, erythropoietic, 2
MONDO:0060724	glycosylphosphatidylinositol biosynthesis defect 17
MONDO:0021127	has a syndromic presentation
MONDO:0021126	syndromic or isolated
MONDO:0008169	osteochondrodysplasia, rhizomelic, with callosal agenesis, thrombocytopenia, hydrocephalus, and hypertension
MONDO:0021125	disease characteristic
MONDO:0060722	neurodevelopmental disorder with brain, liver, and lung abnormalities
MONDO:0021124	female infertility
MONDO:0021123	Ewing sarcoma/peripheral primitive neuroectodermal tumor of bone
MONDO:0008167	dermoid cyst of ovary
MONDO:0060720	congenital disorder of glycosylation with defective fucosylation
MONDO:0008168	ovarian fibroma
MONDO:0021122	small cell neuroendocrine carcinoma
MONDO:0021121	hemangioendothelioma
MONDO:0008165	southeast Asian ovalocytosis
MONDO:0008166	ovalocytosis, hereditary hemolytic, with defective erythropoiesis
MONDO:0021120	functioning endocrine neoplasm
MONDO:0008163	otofaciocervical syndrome
MONDO:0008164	otosclerosis 1
MONDO:0008161	otodental syndrome
MONDO:0008162	otitis media, susceptibility to
MONDO:0021119	non-functioning endocrine neoplasm
MONDO:0008160	osteosclerosis with ichthyosis and fractures
MONDO:0021118	intestinal neoplasm
MONDO:0021117	lung neoplasm
MONDO:0033135	Charcot-Marie-Tooth disease, demyelinating, type 1G
MONDO:0060759	neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures
MONDO:0060758	spinocerebellar ataxia 42, early-onset, severe, with neurodevelopmental deficits
MONDO:0008138	syndromic orbital border hypoplasia
MONDO:0021116	luminal A breast carcinoma
MONDO:0011789	familial meningioma
MONDO:0008139	OSLAM syndrome
MONDO:0021115	luminal B breast carcinoma
MONDO:0008136	isolated optic nerve hypoplasia
MONDO:0021114	Bartholin gland neoplasm
MONDO:0021113	respiratory failure
MONDO:0008137	orofaciodigital syndrome X
MONDO:0008134	autosomal dominant optic atrophy, classic form
MONDO:0021112	scrotum cancer
MONDO:0021111	ureter neoplasm
MONDO:0060752	neurodevelopmental disorder with spasticity and poor growth
MONDO:0008135	optic atrophy 13 with retinal and foveal abnormalities
MONDO:0008132	optic atrophy with demyelinating disease of CNS
MONDO:0021110	sweat gland adenoma
MONDO:0008133	optic atrophy 3
MONDO:0011793	celiac disease, susceptibility to, 5
MONDO:0008130	ophthalmoplegia-intellectual disability-lingua scrotalis syndrome
MONDO:0060760	intellectual developmental disorder with dysmorphic facies and behavioral abnormalities
MONDO:0011792	thyroid dyshormonogenesis 6
MONDO:0008131	optic atrophy, hearing loss, and peripheral neuropathy, autosomal dominant
MONDO:0011795	anonychia-microcephaly syndrome
MONDO:0011794	Dravet syndrome
MONDO:0021109	inverted urothelial papilloma
MONDO:0011797	infantile-onset ascending hereditary spastic paralysis
MONDO:0021108	meningitis
MONDO:0011796	epilepsy, partial, with pericentral spikes
MONDO:0011799	autosomal recessive nonsyndromic deafness 33
MONDO:0021107	narcolepsy
MONDO:0011798	hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration
MONDO:0021106	laminopathy
MONDO:0011791	deafness, autosomal recessive
MONDO:0011790	Amish lethal microcephaly
MONDO:0011779	laryngeal atresia, encephalocele, and limb deformities
MONDO:0021105	NAFLD1
MONDO:0008149	osteogenesis imperfecta with opalescent teeth, blue sclerae and wormian bones but without fractures
MONDO:0011778	multiple epiphyseal dysplasia, Al-Gazali type
MONDO:0060745	intellectual developmental disorder with or without epilepsy or cerebellar ataxia
MONDO:0021104	alcoholic fatty liver disease
MONDO:0021103	collagen diseases
MONDO:0008147	osteogenesis imperfecta type 2
MONDO:0008148	osteogenesis imperfecta type 4
MONDO:0021102	prostate phyllodes tumor
MONDO:0008145	Ollier disease
MONDO:0021101	appendix L-cell glucagon-like peptide-producing neuroendocrine tumor
MONDO:0008146	osteogenesis imperfecta type 1
MONDO:0021100	breast neoplasm
MONDO:0008143	osteoarthritis susceptibility 1
MONDO:0008144	osteochondritis dissecans
MONDO:0011782	angioid streaks
MONDO:0008141	ossicular malformations, familial
MONDO:0008142	Thiemann disease, familial form
MONDO:0011781	spinocerebellar ataxia type 17
MONDO:0011784	Moyamoya disease 2
MONDO:0011783	ALG12-CDG
MONDO:0008140	ossified ear cartilages
MONDO:0011786	allergic rhinitis
MONDO:0011785	hereditary spastic paraplegia 19
MONDO:0011788	cloverleaf skull-multiple congenital anomalies syndrome
MONDO:0011787	autosomal recessive limb-girdle muscular dystrophy type 2I
MONDO:0023757	meralgia paresthetica
MONDO:0011780	specific language impairment 3
MONDO:0021172	Timothy syndrome type 2 (disorder)
MONDO:0021171	Timothy syndrome type 1 (disorder)
MONDO:0021170	amyotonia congenita
MONDO:0021179	proteostasis deficiencies
MONDO:0021178	injury
MONDO:0021177	autoimmune hepatitis type 3
MONDO:0008198	parietal foramina with cleidocranial dysplasia
MONDO:0021176	autoimmune hepatitis type 2
MONDO:0021175	herpetic vulvovaginitis
MONDO:0008199	late-onset Parkinson disease
MONDO:0008196	parastremmatic dwarfism
MONDO:0008197	parietal foramina 1
MONDO:0008194	Paramolar tubercle of bolk
MONDO:0008195	paramyotonia congenita of Von Eulenburg
MONDO:0008192	paragangliomas 1
MONDO:0008193	paralysis agitans, juvenile, of Hunt
MONDO:0008190	human papillomavirus type 18 integration site 1
MONDO:0008191	human papillomavirus type 18 integration site 2
MONDO:0021163	kidney neoplasm
MONDO:0021162	carotenemia
MONDO:0021161	gonococcal prostatitis
MONDO:0021160	gonococcal cystitis
MONDO:0021169	epithelioid hemangioma
MONDO:0021168	hibernoma
MONDO:0021167	myositis
MONDO:0021166	inflammatory disease
MONDO:0021165	Paget disease
MONDO:0021164	posthitis
MONDO:0021152	inherited
MONDO:0021151	non-genetic
MONDO:0021150	genetic characteristic
MONDO:0060715	tumoral calcinosis, hyperphosphatemic, familial, 3
MONDO:0060714	tumoral calcinosis, hyperphosphatemic, familial, 2
MONDO:0060713	deafness, congenital heart defects, and posterior embryotoxon
MONDO:0060712	developmental delay, intellectual disability, obesity, and dysmorphic features
MONDO:0021159	gonococcal salpingitis
MONDO:0021158	gonococcal epididymo-orchitis
MONDO:0060711	Jaberi-Elahi syndrome
MONDO:0021157	gonococcal cervicitis
MONDO:0008178	inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1
MONDO:0021156	hypophysitis
MONDO:0008179	paroxysmal extreme pain disorder
MONDO:0021155	X-linked cone-rod dystrophy
MONDO:0008176	Paget disease of bone 3
MONDO:0021154	dermis disease
MONDO:0008177	extramammary Paget disease
MONDO:0021153	genetic and acquired
MONDO:0008174	pachyonychia congenita 2
MONDO:0008175	pacman dysplasia
MONDO:0008172	hypertrophic osteoarthropathy, primary, autosomal dominant
MONDO:0008173	pachyonychia congenita 1
MONDO:0008170	ovarian cancer
MONDO:0008171	nephrolithiasis
MONDO:0021141	acquired
MONDO:0021140	congenital
MONDO:0060707	Ververi-Brady syndrome
MONDO:0060704	neurodevelopmental disorder with spastic quadriplegia and brain abnormalities with or without seizures
MONDO:0060702	spondyloepimetaphyseal dysplasia, di rocco type
MONDO:0021149	genetic vs non-genetic etiology
MONDO:0021148	female reproductive system neoplasm
MONDO:0021147	disorder of development or morphogenesis
MONDO:0021146	headache disorder
MONDO:0021145	disease of genitourinary system
MONDO:0008189	papillomatosis, florid, of nipple
MONDO:0021144	ovarian clear cell tumor
MONDO:0021143	melanocytic neoplasm
MONDO:0008187	panic disorder 1
MONDO:0008188	papillomatosis, confluent and reticulated
MONDO:0021142	acquired rippling muscle disease
MONDO:0008185	hereditary chronic pancreatitis
MONDO:0008186	pancytopenia and occlusive vascular disease
MONDO:0008183	annular pancreas
MONDO:0008184	pancreas, dorsal, agenesis of
MONDO:0008181	palmaris longus muscle, absence of
MONDO:0008182	nasopalpebral lipoma-coloboma syndrome
MONDO:0008180	congenital velopharyngeal incompetence
MONDO:0021139	congenital or acquired
MONDO:0033116	spinocerebellar ataxia, autosomal recessive 26
MONDO:0033115	spinocerebellar ataxia, autosomal recessive 25
MONDO:0011724	encephalopathy due to GLUT1 deficiency
MONDO:0011723	hemifacial myohyperplasia
MONDO:0011726	peripheral arterial occlusive disease 1
MONDO:0011725	Crigler-Najjar syndrome type 2
MONDO:0011728	blepharospasm
MONDO:0011727	anorexia nervosa, susceptibility to, 1
MONDO:0011729	stroke, susceptibility to, 1
MONDO:0011731	glucose-galactose malabsorption
MONDO:0011730	fumaric aciduria
MONDO:0011733	parasomnia, sleep bruxism type
MONDO:0011732	familial digital arthropathy-brachydactyly
MONDO:0023704	Martinez Monasterio Pinheiro syndrome
MONDO:0011713	melanoma-pancreatic cancer syndrome
MONDO:0011712	van der Woude syndrome 2
MONDO:0011715	Seckel syndrome 2
MONDO:0011714	partial lipodystrophy, congenital cataracts, and neurodegeneration syndrome
MONDO:0011717	hyperinsulinism-hyperammonemia syndrome
MONDO:0011716	acute hemorrhagic leukoencephalitis
MONDO:0011719	gastrointestinal stromal tumor
MONDO:0011718	primary ciliary dyskinesia 2
MONDO:0011720	spermatogenic failure 3
MONDO:0011722	intellectual disability-obesity-prognathism-eye and skin anomalies syndrome
MONDO:0011721	distal myopathy with anterior tibial onset
MONDO:0011709	split hand-foot malformation 5
MONDO:0011702	dilated cardiomyopathy 1L
MONDO:0011701	inflammatory bowel disease 4
MONDO:0011704	glaucoma 1, open angle, B
MONDO:0011703	spongiform encephalopathy with neuropsychiatric features
MONDO:0011706	Kufor-Rakeb syndrome
MONDO:0011705	lymphangioleiomyomatosis
MONDO:0011708	autosomal dominant nonsyndromic deafness 36
MONDO:0011707	familial dyskinesia and facial myokymia
MONDO:0011711	specific language impairment 2
MONDO:0011710	specific language impairment 1
MONDO:0011700	inflammatory bowel disease 6
MONDO:0008118	odontomatosis-aortae esophagus stenosis syndrome
MONDO:0008119	spinocerebellar ataxia type 1
MONDO:0011768	myasthenia gravis with thymus hyperplasia
MONDO:0008116	oculopharyngeal muscular dystrophy
MONDO:0011767	autosomal recessive nonsyndromic deafness 31
MONDO:0008117	oculopharyngodistal myopathy
MONDO:0008114	obsessive-compulsive disorder
MONDO:0008115	Feingold syndrome type 1
MONDO:0011769	familial aortic dissection
MONDO:0008112	Goldenhar syndrome
MONDO:0008113	Schilbach-Rott syndrome
MONDO:0008110	ocular dominance
MONDO:0008111	oculodentodigital dysplasia
MONDO:0011771	distal spinal muscular atrophy type 3
MONDO:0011770	aortic aneurysm, familial thoracic 2
MONDO:0011773	anauxetic dysplasia
MONDO:0011772	B4GALT1-CDG
MONDO:0011775	nasopharyngeal carcinoma, susceptibility to, 1
MONDO:0011774	autosomal recessive nonsyndromic deafness 30
MONDO:0011777	Alzheimer disease 8
MONDO:0011776	CINCA syndrome
MONDO:0008129	ophthalmoplegia, familial total, with iris transillumination
MONDO:0008127	ophthalmomandibulomelic dysplasia
MONDO:0011757	brachydactyly type A1B
MONDO:0008128	ophthalmoplegia, familial static
MONDO:0011756	Senior-Loken syndrome 4
MONDO:0011759	Hurler-Scheie syndrome
MONDO:0008125	nonsyndromic congenital nail disorder 5
MONDO:0011758	Hurler syndrome
MONDO:0008126	oncogene Yuasa
MONDO:0008123	autosomal dominant omodysplasia
MONDO:0008124	omphalocele, autosomal
MONDO:0008121	onychogryposis, pedal, with keratosis plantaris and coarse hair
MONDO:0008122	olivopontocerebellar atrophy 5
MONDO:0011760	Scheie syndrome
MONDO:0008120	spinocerebellar ataxia type 7
MONDO:0011762	autosomal recessive nonsyndromic deafness 22
MONDO:0011761	autosomal dominant nonsyndromic deafness 21
MONDO:0011764	autosomal dominant Parkinson disease 8
MONDO:0011763	T-box 24
MONDO:0011766	46,XY gonadal dysgenesis-motor and sensory neuropathy syndrome
MONDO:0011765	multiple epiphyseal dysplasia type 5
MONDO:0011746	symphalangism, distal, with microdontia, dental pulp stones, and narrowed zygomatic arch
MONDO:0011745	duodenojejunal atresia with volvulus, absent dorsal mesentery, and absent superior mesenteric artery
MONDO:0011748	Usher syndrome type 1G
MONDO:0011747	dyslexia, susceptibility to, 5
MONDO:0011749	oculocutaneous albinism type 1B
MONDO:0011751	COPD, severe early onset
MONDO:0011750	insulinoma tumor suppressor gene locus
MONDO:0011753	epilepsy, idiopathic generalized, susceptibility to, 2
MONDO:0011752	nephronophthisis 4
MONDO:0011755	senior-loken syndrome 3
MONDO:0011754	familial hyperreninemic hypoaldosteronism type 2
MONDO:0023726	mediastinal yolk sac tumor
MONDO:0008109	ocular cicatricial pemphigoid
MONDO:0008107	nystagmus, hereditary vertical
MONDO:0008108	oculocerebrocutaneous syndrome
MONDO:0008105	nose, anomalous shape of
MONDO:0011735	hyper-IgM syndrome type 3
MONDO:0008106	nystagmus 2, congenital, autosomal dominant
MONDO:0011734	Cardioneuromyopathy with hyaline masses and nemaline rods
MONDO:0008103	noduli Cutanei, multiple, with urinary tract abnormalities
MONDO:0011737	parkinson disease 10
MONDO:0008104	Noonan syndrome 1
MONDO:0011736	Cree intellectual disability syndrome
MONDO:0008101	familial supernumerary nipples
MONDO:0011739	pancreatic cancer, susceptibility to, 1
MONDO:0008102	sick sinus syndrome 2, autosomal dominant
MONDO:0011738	bilateral frontoparietal polymicrogyria
MONDO:0008100	nipples inverted
MONDO:0011740	Carney-Stratakis syndrome
MONDO:0011742	hirschsprung disease, susceptibility to, 7
MONDO:0011741	hirschsprung disease, susceptibility to, 6
MONDO:0011744	primary intraosseous venous malformation
MONDO:0011743	Alzheimer disease 4
MONDO:0011809	mammographic density
MONDO:0011808	cataract 27
MONDO:0011801	spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 1
MONDO:0011800	glioma susceptibility 4
MONDO:0011803	hereditary spastic paraplegia 7
MONDO:0011802	hypercalciuria, absorptive, 1
MONDO:0011805	asthma-related traits, susceptibility to, 1
MONDO:0011804	autoimmune lymphoproliferative syndrome type 2B
MONDO:0011807	systemic lupus erythematosus with hemolytic anemia, susceptibility to, 1
MONDO:0011806	osteofibrous dysplasia
MONDO:0011810	horizontal gaze palsy with progressive scoliosis
MONDO:0021196	disease by molecular activity disrupted
MONDO:0021195	disease by cellular process disrupted
MONDO:0021194	disease by subcellular system affected
MONDO:0021193	neuroepithelial neoplasm
MONDO:0021192	odontogenic neoplasm
MONDO:0021191	malignant ependymoma
MONDO:0021190	DNA repair disease
MONDO:0021199	disease by anatomical system
MONDO:0021198	rare genetic disease
MONDO:0021197	disease by cellular component affected
MONDO:0021184	deltaretrovirus infections
MONDO:0021183	HTLV-2 infection
MONDO:0021181	inherited blood coagulation disorder
MONDO:0021180	acquired xanthinuria
MONDO:0021189	intestinal motility disease
MONDO:0021188	hemangiopericytoma
MONDO:0021187	hyperlipidemia
MONDO:0060779	acquired Fanconi syndrome
MONDO:0060778	adult Fanconi syndrome
MONDO:0060777	cervical fibroepithelial polyp
MONDO:0060774	vaginal fibroepithelial polyp
MONDO:0060782	premalignant hematological system disease
MONDO:0060781	Preeyasombat-Varavithya syndrome
MONDO:0060768	gingival fibroepithelial polyp
MONDO:0060766	anal polyp
MONDO:0060765	fibroepithelial polyp
MONDO:0060764	tetraamelia syndrome 1
MONDO:0060763	intellectual developmental disorder with speech delay, dysmorphic facies, and t-cell abnormalities
MONDO:0060761	neurodevelopmental disorder with epilepsy and hypoplasia of the corpus callosum
MONDO:0033187	combined oxidative phosphorylation defect type 29
MONDO:0060783	classic congenital adrenal hyperplasia
MONDO:0033196	skin/hair/eye pigmentation, variation in
MONDO:0033198	deafness, autosomal recessive 106
MONDO:0033199	deafness, autosomal recessive 107
MONDO:0023679	hematohidrosis
MONDO:0008039	tropical spastic paraparesis
MONDO:0021017	synaptopathy
MONDO:0021016	channelopathy
MONDO:0008037	myelinated optic nerve fibers
MONDO:0008038	ataxia-pancytopenia syndrome
MONDO:0060611	combined immunodeficiency and megaloblastic anemia with or without hyperhomocysteinemia
MONDO:0008035	muscular hypoplasia, congenital universal, of Krabbe
MONDO:0021013	trichothiodystrophy 4, nonphotosensitive
MONDO:0008036	myasthenia, limb-girdle, autoimmune
MONDO:0021012	susceptibility to visceral leishmaniasis, 1
MONDO:0021011	hereditary progressive chorea without dementia
MONDO:0008033	autosomal dominant limb-girdle muscular dystrophy type 1B
MONDO:0023670	Bardet-Biedl syndrome 20
MONDO:0021010	skin lymphangiosarcoma
MONDO:0008034	muscular dystrophy, pseudohypertrophic, with Internalized capillaries
MONDO:0023671	oculopharyngodistal myopathy 3
MONDO:0011694	spinocerebellar ataxia type 15/16
MONDO:0008031	facioscapulohumeral muscular dystrophy 2
MONDO:0011693	glaucoma, normal tension, susceptibility to
MONDO:0008032	autosomal dominant limb-girdle muscular dystrophy type 1A
MONDO:0011696	melanoma, uveal, susceptibility to, 2
MONDO:0011695	melanoma, uveal, susceptibility to, 1
MONDO:0008030	facioscapulohumeral muscular dystrophy 1
MONDO:0011698	glycine N-methyltransferase deficiency
MONDO:0011697	Waardenburg syndrome type 2C
MONDO:0021009	salivary gland mucoepidermoid carcinoma
MONDO:0021008	secondary antiphospholipid syndrome
MONDO:0011699	inflammatory bowel disease 8
MONDO:0021007	stage of disease
MONDO:0033006	Galloway-Mowat syndrome 2, X-linked
MONDO:0033007	Galloway-Mowat syndrome 3
MONDO:0033004	polycystic kidney disease 4
MONDO:0033005	Galloway-Mowat syndrome 1
MONDO:0011690	Camurati-Engelmann disease, type 2
MONDO:0011692	basal ganglia calcification, idiopathic, 2
MONDO:0011691	amyotrophic lateral sclerosis type 3
MONDO:0023662	lymphatic malformation 10
MONDO:0023663	macrocephaly mesodermal hamartoma spectrum
MONDO:0023664	spermatogenic failure 54
MONDO:0033008	Galloway-Mowat syndrome 4
MONDO:0033009	Galloway-Mowat syndrome 5
MONDO:0021005	faciodigitogenital syndrome
MONDO:0011679	craniosynostosis syndrome, autosomal recessive
MONDO:0021004	brachydactyly
MONDO:0008048	autosomal dominant centronuclear myopathy
MONDO:0021003	polydactyly
MONDO:0008049	myopathy, distal, infantile-onset
MONDO:0021002	syndactyly
MONDO:0008046	autosomal dominant myoglobinuria
MONDO:0021001	hemochromatosis type 1
MONDO:0008047	episodic ataxia type 1
MONDO:0008044	myoclonic dystonia 11
MONDO:0008045	spinal muscular atrophy-progressive myoclonic epilepsy syndrome
MONDO:0023660	angioedema, hereditary, 6
MONDO:0011683	oculocutaneous albinism type 4
MONDO:0008042	myoclonus and ataxia
MONDO:0011682	episodic ataxia type 3
MONDO:0033010	erythrokeratodermia variabilis et progressiva 1
MONDO:0008043	myoclonus-cerebellar ataxia-deafness syndrome
MONDO:0008040	transient myeloproliferative syndrome
MONDO:0011685	polysubstance abuse, susceptibility to
MONDO:0011684	vitiligo-associated multiple autoimmune disease susceptibility 1
MONDO:0008041	myoclonic epilepsy, Hartung type
MONDO:0011687	Charcot-Marie-Tooth disease axonal type 2F
MONDO:0011686	DNA ligase IV deficiency
MONDO:0011689	dyslexia, susceptibility to, 6
MONDO:0011688	muscular dystrophy-dystroglycanopathy type B5
MONDO:0023659	developmental and epileptic encephalopathy 96
MONDO:0033015	erythrokeratodermia variabilis et progressiva 5
MONDO:0033013	erythrokeratodermia variabilis et progressiva 3
MONDO:0033014	erythrokeratodermia variabilis et progressiva 4
MONDO:0011681	episodic ataxia type 4
MONDO:0033012	erythrokeratodermia variabilis et progressiva 2
MONDO:0011680	autosomal recessive congenital ichthyosis 3
MONDO:0023650	littoral cell angioma of the spleen
MONDO:0023655	immunodeficiency 14b, autosomal recessive
MONDO:0008019	mullerian aplasia and hyperandrogenism
MONDO:0023657	intellectual developmental disorder, autosomal dominant 65
MONDO:0008017	hereditary mucoepithelial dysplasia
MONDO:0011669	hypotonia-cystinuria syndrome
MONDO:0011668	maturity-onset diabetes of the young type 6
MONDO:0008018	Muir-Torre syndrome
MONDO:0008015	motion sickness
MONDO:0045008	cholesterol metabolism disease
MONDO:0008016	trismus-pseudocamptodactyly syndrome
MONDO:0008013	chromosome 9p deletion syndrome
MONDO:0045002	vertebral disease
MONDO:0008014	nondisjunction
MONDO:0045001	cardiac ventricle disease
MONDO:0060631	Alkuraya-Kucinskas syndrome
MONDO:0045004	skeletal ligament disease
MONDO:0008011	antigen defined by monoclonal antibody T87
MONDO:0045003	scrotal disease
MONDO:0008012	Monophalangy of great toe
MONDO:0011672	persistent polyclonal B-cell lymphocytosis
MONDO:0011671	Huntington disease-like 2
MONDO:0008010	antigen defined by monoclonal antibody Aj9
MONDO:0011674	Charcot-Marie-Tooth disease dominant intermediate B
MONDO:0011673	autosomal dominant nonsyndromic deafness 30
MONDO:0011676	PHACE syndrome
MONDO:0011675	Charcot-Marie-Tooth Disease, axonal, type 2GG
MONDO:0011678	homozygous 11P15-p14 deletion syndrome
MONDO:0011677	Megarbane syndrome
MONDO:0011670	Ehlers-Danlos syndrome due to tenascin-X deficiency
MONDO:0045011	keratinization disease
MONDO:0023642	Weber syndrome
MONDO:0045010	glycoprotein metabolism disease
MONDO:0060629	neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal recessive
MONDO:0023644	lip and oral cavity carcinoma
MONDO:0060627	glycosylphosphatidylinositol biosynthesis defect 15
MONDO:0023646	lipodermatosclerosis
MONDO:0045017	cholesterol biosynthetic process disease
MONDO:0011658	autosomal recessive early-onset Parkinson disease 7
MONDO:0008028	muscular dystrophy, Barnes type
MONDO:0045016	cholesterol catabolic process disease
MONDO:0011657	autosomal dominant nonsyndromic deafness 24
MONDO:0008029	Bethlem myopathy
MONDO:0060624	neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter
MONDO:0008026	autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures
MONDO:0045019	lactation disease
MONDO:0008027	muscular atrophy, malignant neurogenic
MONDO:0011659	heterotaxy, visceral, 3, autosomal
MONDO:0045018	creatine biosynthetic process disease
MONDO:0060622	neurodevelopmental disorder with severe motor impairment and absent language
MONDO:0008024	neuronopathy, distal hereditary motor, type 7A
MONDO:0045013	disease of extraembryonic membrane
MONDO:0060621	neurodevelopmental disorder with microcephaly, seizures, and cortical atrophy
MONDO:0045012	steroid metabolism disease
MONDO:0008025	neuronopathy, distal hereditary motor, type 2A
MONDO:0008022	muscle cramps, familial
MONDO:0045015	carbohydrate transport disease
MONDO:0008023	muscular atrophy-ataxia-retinitis pigmentosa-diabetes mellitus syndrome
MONDO:0045014	tetrahydrobiopterin metabolic process disease
MONDO:0011661	inflammatory bowel disease 5
MONDO:0008020	multiple exostoses with spastic tetraparesis
MONDO:0008021	Cowden syndrome 1
MONDO:0011660	autosomal dominant nonsyndromic deafness 22
MONDO:0011663	juvenile primary lateral sclerosis
MONDO:0011662	pathological gambling
MONDO:0011665	Lennox-Gastaut syndrome
MONDO:0011664	immunodeficiency due to CD25 deficiency
MONDO:0011667	maturity-onset diabetes of the young type 4
MONDO:0011666	maturity-onset diabetes of the young
MONDO:0021053	carotid body paraganglioma
MONDO:0021052	parasympathetic paraganglioma
MONDO:0021051	hemophagocytic syndrome
MONDO:0021050	vaginal neoplasm
MONDO:0021059	head or neck disease/disorder
MONDO:0021058	neoplastic syndrome
MONDO:0008079	neurofibromatosis-pheochromocytoma-duodenal carcinoid syndrome
MONDO:0021057	classic or attenuated familial adenomatous polyposis
MONDO:0021056	familial adenomatous polyposis 1
MONDO:0021055	classic familial adenomatous polyposis
MONDO:0008077	neurofibromatosis, type 1
MONDO:0008078	neurofibromatosis, familial spinal
MONDO:0021054	bone sarcoma
MONDO:0008075	neurofibromatosis type 3
MONDO:0008076	amyotrophic neuralgia
MONDO:0008073	familial juvenile hyperuricemic nephropathy type 1
MONDO:0008074	nerve growth factor, alpha subunit
MONDO:0008071	autosomal dominant progressive nephropathy with hypertension
MONDO:0008072	IgA nephropathy, susceptibility to, 1
MONDO:0008070	nemaline myopathy 3
MONDO:0021042	glioma
MONDO:0021041	pleural solitary fibrous tumor
MONDO:0021040	pancreatic neoplasm
MONDO:0021049	vulvar neoplasm
MONDO:0021048	benign mastocytoma
MONDO:0021047	breast phyllodes tumor
MONDO:0021046	breast fibroepithelial neoplasm
MONDO:0021045	fibroepithelial neoplasm
MONDO:0008088	neuropathy, with paraprotein in serum, cerebrospinal fluid and urine
MONDO:0021044	Wilms tumor
MONDO:0008089	neutropenia, chronic familial
MONDO:0021043	mixed neoplasm
MONDO:0008086	neuropathy, hereditary sensory and autonomic, type 1A
MONDO:0008087	hereditary neuropathy with liability to pressure palsies
MONDO:0008084	neuropathy, congenital, with arthrogryposis multiplex
MONDO:0008085	neuropathy, hereditary sensorimotor, with upper motor neuron, visual pathway and autonomic disturbance
MONDO:0008082	multiple endocrine neoplasia type 2B
MONDO:0008083	neuronal ceroid lipofuscinosis 4B
MONDO:0008080	neurofibromatosis, type III, mixed central and peripheral
MONDO:0008081	neurofibromatosis, type IV, of Riccardi
MONDO:0023696	Marinesco-Sjogren-like syndrome
MONDO:0023699	Maroteaux Fonfria syndrome
MONDO:0021039	extraskeletal Ewing sarcoma/peripheral primitive neuroectodermal tumor
MONDO:0021038	Ewing sarcoma/peripheral primitive neuroectodermal tumor
MONDO:0008059	Naegeli-Franceschetti-Jadassohn syndrome
MONDO:0021037	genetic neurodegenerative disease with dementia
MONDO:0021036	keratosis pilaris
MONDO:0008057	Carney complex, type 1
MONDO:0021035	alopecia-intellectual disability syndrome 1
MONDO:0008058	cylindrical spirals myopathy
MONDO:0023691	maple syrup urine disease type 1A
MONDO:0021034	genetic alopecia
MONDO:0008055	myotonia congenita, autosomal dominant
MONDO:0021033	herpes zoster dermatitis
MONDO:0023692	maple syrup urine disease type 1B
MONDO:0008056	myotonic dystrophy type 1
MONDO:0023693	maple syrup urine disease type 2
MONDO:0021032	herpes zoster with dermatitis of eyelid
MONDO:0008053	myopia 2, autosomal dominant
MONDO:0008054	juvenile dermatomyositis
MONDO:0008051	tubular aggregate myopathy
MONDO:0008052	myopathy with storage of glycoproteins and Glycosaminoglycans
MONDO:0008050	MYH7-related skeletal myopathy
MONDO:0021029	genetic sebaceous gland anomaly
MONDO:0021020	Crigler-Najjar syndrome type 1
MONDO:0021028	genetic nail anomaly
MONDO:0021027	genetic hair anomaly
MONDO:0021026	genetic epidermal appendage anomaly
MONDO:0021025	cirrhosis, familial, with antigenemia
MONDO:0021024	malaria, susceptibility to
MONDO:0008068	navicular bone, accessory
MONDO:0008069	necrotizing encephalomyelopathy, subacute, of Leigh, adult
MONDO:0021023	complete androgen insensitivity syndrome
MONDO:0021022	hereditary hyperekplexia
MONDO:0008066	nasal hyperpigmentation, familial transverse
MONDO:0021021	craniodiaphyseal dysplasia, autosomal dominant
MONDO:0023682	tympanic paraganglioma
MONDO:0008067	nasopharyngeal carcinoma, susceptibility to, 2
MONDO:0008064	nasal bones, absence of
MONDO:0008065	nasal groove, familial transverse
MONDO:0008062	narcolepsy 1
MONDO:0008063	nasal alar collapse, bilateral
MONDO:0008060	nonsyndromic congenital nail disorder 1
MONDO:0008061	nail-patella syndrome
MONDO:0021019	X-linked recessive ocular albinism
MONDO:0021018	autosomal dominant limb-girdle muscular dystrophy type 1D (DNAJB6)
MONDO:0011603	GNE myopathy
MONDO:0011602	autosomal recessive nonsyndromic deafness 27
MONDO:0011605	generalized basaloid follicular hamartoma syndrome
MONDO:0011604	spondylo-ocular syndrome
MONDO:0011607	narcolepsy 2, susceptibility to
MONDO:0011606	baby rattle pelvis dysplasia
MONDO:0011609	atopic dermatitis 6
MONDO:0011608	atopic dermatitis 5
MONDO:0011610	dimethylglycine dehydrogenase deficiency
MONDO:0011612	glycine encephalopathy
MONDO:0011611	short stature, intellectual disability, callosal agenesis, Heminasal hypoplasia, microphthalmia, and atypical clefting
MONDO:0011601	neonatal intrahepatic cholestasis due to citrin deficiency
MONDO:0011600	congenital myasthenic syndrome 4A
MONDO:0011647	Alzheimer disease 7
MONDO:0011646	laryngeal abductor paralysis with cerebellar ataxia and motor neuropathy
MONDO:0011649	AVSD 1
MONDO:0011648	radiation-induced meningioma
MONDO:0011650	atrioventricular septal defect, susceptibility to, 2
MONDO:0011652	Phelan-McDermid syndrome
MONDO:0011651	intellectual disability, short stature, facial anomalies, and joint dislocations
MONDO:0011654	intellectual disability, microcephaly, growth retardation, joint contractures, and facial dysmorphism
MONDO:0011653	thyroid cancer, nonmedullary, 3
MONDO:0011656	paget disease of bone 4
MONDO:0011655	alveolar soft part sarcoma
MONDO:0023628	levator syndrome
MONDO:0008008	MOMO syndrome
MONDO:0008009	monilethrix
MONDO:0008006	Mobius syndrome
MONDO:0011636	Diamond-Blackfan anemia 2
MONDO:0011635	goiter, multinodular 3
MONDO:0008007	tooth ankylosis
MONDO:0008004	familial mitral valve prolapse
MONDO:0011638	neuroferritinopathy
MONDO:0008005	cardiospondylocarpofacial syndrome
MONDO:0011637	Sener syndrome
MONDO:0008002	mirror movements 1
MONDO:0008003	autosomal dominant progressive external ophthalmoplegia
MONDO:0011639	Diamond-Blackfan anemia 15 with mandibulofacial dysostosis
MONDO:0008000	migraine with or without aura, susceptibility to, 1
MONDO:0008001	milia, multiple eruptive
MONDO:0011641	baculum, congenital absence of
MONDO:0011640	genitopatellar syndrome
MONDO:0011643	permanent neonatal diabetes mellitus
MONDO:0011642	carnitine acetyltransferase deficiency
MONDO:0011645	aneurysmal bone cysts
MONDO:0011644	pars planitis
MONDO:0023616	familial leiomyomatosis
MONDO:0023619	lentigo maligna melanoma
MONDO:0011625	autosomal dominant nonsyndromic deafness 18
MONDO:0011624	transaldolase deficiency
MONDO:0011627	autism, susceptibility to, 5
MONDO:0011626	acromegaloid features, overgrowth, cleft palate, and hernia
MONDO:0011629	MOGS-CDG
MONDO:0011628	propionic acidemia
MONDO:0011630	retinitis pigmentosa 28
MONDO:0011632	amyotrophic lateral sclerosis type 21
MONDO:0011631	hemochromatosis type 4
MONDO:0011634	rippling muscle disease
MONDO:0011633	Charcot-Marie-Tooth disease axonal type 2C
MONDO:0023603	hereditary disorder of connective tissue
MONDO:0023605	Laugier-Hunziker syndrome
MONDO:0023607	Laurence-Prosser-Rocker syndrome
MONDO:0023609	le Marec-Bracq-Picaud syndrome
MONDO:0023601	non-classic congenital adrenal hyperplasia
MONDO:0011614	3-hydroxy-3-methylglutaryl-CoA synthase deficiency
MONDO:0011613	autosomal recessive early-onset Parkinson disease 6
MONDO:0011616	holoprosencephaly 6
MONDO:0011615	East Texas bleeding disorder
MONDO:0011618	liver fibrocystic disease and polydactyly
MONDO:0011617	arthropathy, erosive
MONDO:0011619	crumpled helices and small mouth
MONDO:0011621	acropectoral syndrome
MONDO:0011620	metaphyseal dysplasia, Braun-Tinschert type
MONDO:0011623	spinocerebellar ataxia, autosomal recessive 1
MONDO:0011622	nephrolithiasis, uric acid, susceptibility to
MONDO:0021097	intraductal breast papilloma
MONDO:0021096	papillary epithelial neoplasm
MONDO:0045063	major salivary gland adenoid cystic carcinoma
MONDO:0021095	parkinsonian disorder
MONDO:0021094	immunodeficiency disease
MONDO:0021093	cranioectodermal dysplasia 1
MONDO:0045060	intraductal cribriform breast adenocarcinoma
MONDO:0021092	fallopian tube neoplasm
MONDO:0021091	papillary cystadenoma
MONDO:0021090	lipid-rich breast carcinoma
MONDO:0045068	minor salivary gland adenoid cystic carcinoma
MONDO:0021099	intraductal papillomatosis
MONDO:0045069	minor salivary gland carcinoma
MONDO:0021098	papillomatosis
MONDO:0021086	gingival neoplasm
MONDO:0021085	gastric neoplasm
MONDO:0021084	vision disorder
MONDO:0021083	congenital fibrosis of extraocular muscles type 1
MONDO:0045071	mycosis fungoides variant
MONDO:0021082	Meckel diverticulum neoplasm
MONDO:0045070	digestive system melanoma
MONDO:0021081	anti-NMDA receptor encephalitis
MONDO:0021080	blood vessel neoplasm
MONDO:0045072	ectopic hormone secretion syndrome associated with neoplasia
MONDO:0060688	hyperthyroxinemia, euthyroid, caused by generalized 5-prime-deiodinase deficiency
MONDO:0021089	peripheral nervous system cancer
MONDO:0021088	papillary meningioma
MONDO:0021087	malignant granular cell myoblastoma
MONDO:0060690	phenytoin toxicity
MONDO:0033091	ichthyosis, congenital, autosomal recessive 14
MONDO:0033092	ichthyosis, congenital, autosomal recessive 13
MONDO:0021075	neoplastic polyp
MONDO:0021074	precancerous condition
MONDO:0021073	paraneoplastic syndrome
MONDO:0021072	sympathetic paraganglioma
MONDO:0021071	laryngeal neoplasm
MONDO:0021070	sublingual gland carcinoma
MONDO:0021079	childhood neoplasm
MONDO:0021078	glandular papilloma
MONDO:0021077	cystic neoplasm
MONDO:0008099	congenital stationary night blindness autosomal dominant 2
MONDO:0021076	pancreatic exocrine neoplasm
MONDO:0008097	linear nevus sebaceus syndrome
MONDO:0008098	mesomelic dwarfism, Nievergelt type
MONDO:0008095	nevus anemicus
MONDO:0008096	nevus flammeus of nape of neck
MONDO:0008093	nevus, epidermal
MONDO:0008094	familial multiple nevi flammei
MONDO:0008091	abnormal neutrophil chemotactic response
MONDO:0008092	hereditary neutrophilia
MONDO:0008090	cyclic hematopoiesis
MONDO:0021064	jugulotympanic paraganglioma
MONDO:0021063	malignant colon neoplasm
MONDO:0021062	hereditary acrokeratotic poikiloderma of Kindler-Weary
MONDO:0021061	neurofibromatosis
MONDO:0021060	RASopathy
MONDO:0021069	malignant endocrine neoplasm
MONDO:0021068	ovarian neoplasm
MONDO:0021067	mediastinal germ cell tumor
MONDO:0021066	urinary system neoplasm
MONDO:0021065	pleural neoplasm
MONDO:0045020	glycine metabolism disease
MONDO:0045022	disorder of organic acid metabolism
MONDO:0045021	sucrose intolerance disease
MONDO:0060659	neurodevelopmental disorder with poor language and loss of hand skills
MONDO:0045028	radiation or chemically induced disorder
MONDO:0045029	Deuteromycetes infectious disease
MONDO:0045024	cancer or benign tumor
MONDO:0045023	acquired adrenogenital syndrome
MONDO:0033043	spastic ataxia 8, autosomal recessive, with hypomyelinating leukodystrophy
MONDO:0033046	Meier-Gorlin syndrome 8
MONDO:0033047	Perrault syndrome 6
MONDO:0033044	Meckel syndrome 13
MONDO:0033045	orofaciodigital syndrome 16
MONDO:0045031	infectious diarrheal disease
MONDO:0045030	non-infectious diarrheal disease
MONDO:0045033	opportunistic systemic mycosis
MONDO:0045032	congenital secretory diarrhea
MONDO:0060649	short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies
MONDO:0045039	systemic basidiobolomycosis
MONDO:0045038	cutaneous basidiobolomycosis
MONDO:0045035	opportunistic infectious
MONDO:0060642	neurodevelopmental disorder with movement abnormalities, abnormal gait, and autistic features
MONDO:0045034	infectious disease characteristic
MONDO:0045037	hyalohyphomycosis
MONDO:0060641	neurodevelopmental disorder with or without seizures and gait abnormalities
MONDO:0045036	primary infectious
MONDO:0060640	neurodevelopmental disorder with microcephaly, epilepsy, and brain atrophy
MONDO:0060650	Leber congenital amaurosis with early-onset deafness
MONDO:0045042	restricted to specific location
MONDO:0045044	ligament disease
MONDO:0045043	disease of uterine broad ligament
MONDO:0045040	locational disease characteristic
MONDO:0045049	hypermature cataract
MONDO:0060677	chromosome 1p35 deletion syndrome
MONDO:0045046	inherited thyroid metabolism disease
MONDO:0045045	selective IgG immunodeficiency
MONDO:0045048	toxemia of pregnancy
MONDO:0045047	neurosarcoidosis
MONDO:0045053	osteogenic neoplasm
MONDO:0045052	benign osteogenic neoplasm
MONDO:0045055	glycogen-rich carcinoma
MONDO:0045054	cancer-related condition
MONDO:0045051	cortical cataract
MONDO:0045050	nuclear cataract
MONDO:0060666	hypotonia, ataxia, developmental delay, and tooth enamel defect syndrome
MONDO:0045057	delirium
MONDO:0045056	grade II meningioma
MONDO:0060664	neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities
MONDO:0060663	congenital heart defects, multiple types, 5
MONDO:0045059	cribriform carcinoma of breast
MONDO:0060662	Diamond-Blackfan anemia-like
MONDO:0045058	ACTH-producing pituitary gland neoplasm
MONDO:0060671	epilepsy, juvenile myoclonic, susceptibility to, 10
MONDO:0060670	amyotrophic lateral sclerosis, susceptibility to, 25
MONDO:0023551	C1q nephropathy
MONDO:0023554	acquired testicular failure
MONDO:0023557	infective vaginitis
MONDO:0023558	Kocher-debre-Semelaigne syndrome
MONDO:0011569	Charcot-Marie-Tooth disease type 2B1
MONDO:0011573	psoriasis 7, susceptibility to
MONDO:0011572	type 1 diabetes mellitus 18
MONDO:0011575	cerebrooculonasal syndrome
MONDO:0011574	tetralogy of fallot syndrome, autosomal recessive
MONDO:0011577	myopathy, proximal, and ophthalmoplegia
MONDO:0011576	familial hyperaldosteronism type II
MONDO:0011579	late-onset retinal degeneration
MONDO:0011578	familial papillary thyroid carcinoma with renal papillary neoplasia
MONDO:0011571	deafness, autosomal dominant 39, with dentinogenesis imperfecta 1
MONDO:0011570	Charcot-Marie-Tooth disease type 2B2
MONDO:0023540	Kashani-Strom-Utley syndrome
MONDO:0023541	Kasznica-Carlson-Coppedge syndrome
MONDO:0023543	Katsantoni-Papadakou-Lagoyanni syndrome
MONDO:0011559	benign recurrent intrahepatic cholestasis type 2
MONDO:0011558	Usher syndrome type 2C
MONDO:0011562	autosomal dominant Parkinson disease 4
MONDO:0011561	Alzheimer disease 6
MONDO:0011564	cone-rod dystrophy 8
MONDO:0011563	fibromatosis, gingival, 2
MONDO:0011566	abdominal obesity-metabolic syndrome quantitative trait locus 2
MONDO:0011565	metabolic syndrome X
MONDO:0011568	autosomal dominant nonsyndromic deafness 25
MONDO:0011567	dilated cardiomyopathy 1K
MONDO:0023538	Kaplowitz-Bodurtha syndrome
MONDO:0011560	systemic lupus erythematosus, susceptibility to, 3
MONDO:0023530	kallikrein hypertension
MONDO:0011548	cerebral palsy, ataxic, autosomal recessive
MONDO:0011547	cataract 31 multiple types
MONDO:0011549	hypotrichosis 1
MONDO:0060510	Cohen-Gibson syndrome
MONDO:0011551	TH-deficient dopa-responsive dystonia
MONDO:0011550	fibromatosis, gingival, with hypertrichosis and intellectual disability
MONDO:0011553	autosomal recessive nonsyndromic deafness 26
MONDO:0011552	schizophrenia 10
MONDO:0011555	radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome
MONDO:0011554	deafness, nonsyndromic, modifier 1
MONDO:0011557	radiation sensitivity/chromosome instability syndrome, autosomal dominant
MONDO:0011556	basal cell carcinoma, susceptibility to, 1
MONDO:0023528	KSHV inflammatory cytokine syndrome
MONDO:0023521	Judge Misch wright syndrome
MONDO:0060507	retinal dystrophy with or without macular staphyloma
MONDO:0011537	macrocephaly-autism syndrome
MONDO:0011536	optic atrophy 4
MONDO:0060502	neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies
MONDO:0011539	nemaline myopathy 5
MONDO:0011538	frontoocular syndrome
MONDO:0011540	spinocerebellar ataxia type 14
MONDO:0011542	psoriasis 6, susceptibility to
MONDO:0011541	dilated cardiomyopathy 1J
MONDO:0011544	paragangliomas 3
MONDO:0011543	BRCA3
MONDO:0011546	heterotaxy, visceral, 2, autosomal
MONDO:0011545	autosomal dominant nocturnal frontal lobe epilepsy 3
MONDO:0023595	congenital myotonic dystrophy
MONDO:0023597	laryngeal papillomatosis
MONDO:0023599	mesomelic dysplasia
MONDO:0023581	Kuster syndrome
MONDO:0023573	Kozlowski Warren Fisher syndrome
MONDO:0023575	Krauss Herman Holmes syndrome
MONDO:0023577	Krieble Bixler syndrome
MONDO:0023579	Kuster Majewski Hammerstein syndrome
MONDO:0023571	Kozlowski Rafinski Klicharska syndrome
MONDO:0011595	nonsyndromic congenital nail disorder 7
MONDO:0011594	ovarian dysgenesis, hypergonadotropic, with short stature and recurrent metabolic acidosis
MONDO:0011597	atopic dermatitis 3
MONDO:0011596	atopic dermatitis 2
MONDO:0011599	birdshot chorioretinopathy
MONDO:0011598	atopic dermatitis 4
MONDO:0011591	cataract 26 multiple types
MONDO:0011590	anisomastia
MONDO:0011593	seizures, benign familial infantile, 2
MONDO:0011592	exudative vitreoretinopathy 3
MONDO:0023563	Kotzot-Richter syndrome
MONDO:0023567	Kozlowski Brown Hardwick syndrome
MONDO:0023569	Kozlowski Ouvrier syndrome
MONDO:0023561	Koone-Rizzo-Elias syndrome
MONDO:0011584	Fanconi anemia complementation group D1
MONDO:0011583	cerebral amyloid angiopathy, APP-related
MONDO:0011586	otosclerosis 2
MONDO:0011585	autosomal recessive distal spinal muscular atrophy 2
MONDO:0011588	platelet-type bleeding disorder 12
MONDO:0011587	cataract 25
MONDO:0011589	microphthalmia with coloboma 2
MONDO:0011580	cerebellar ataxia and hypergonadotropic hypogonadism
MONDO:0011582	multiple mitochondrial dysfunctions syndrome 1
MONDO:0011581	arrhythmogenic cardiomyopathy with woolly hair and keratoderma
MONDO:0023510	Jaffer-Beighton syndrome
MONDO:0023513	Jeune syndrome situs inversus
MONDO:0011526	Sebastian syndrome
MONDO:0011525	Carney complex type 2
MONDO:0011528	hyper-IgM syndrome type 2
MONDO:0011527	Charcot-Marie-Tooth disease type 4E
MONDO:0011529	spinocerebellar ataxia type 13
MONDO:0011531	Noonan syndrome 2
MONDO:0011530	mesomelic dysplasia, Savarirayan type
MONDO:0011533	temtamy preaxial brachydactyly syndrome
MONDO:0011532	hereditary spastic paraplegia 13
MONDO:0011535	split hand-foot malformation 4
MONDO:0011534	Charcot-Marie-Tooth disease type 4G
MONDO:0011515	papillary renal cell carcinoma
MONDO:0011514	tricuspid atresia
MONDO:0011517	pseudohyperaldosteronism type 2
MONDO:0011516	early response to neural induction gene
MONDO:0011519	autosomal dominant nonsyndromic deafness 23
MONDO:0011518	Wiedemann-Steiner syndrome
MONDO:0011520	systemic lupus erythematosus, susceptibility to, 2
MONDO:0011522	hereditary spastic paraplegia 14
MONDO:0011521	inflammatory bowel disease 7
MONDO:0011524	Dianzani autoimmune lymphoproliferative disease
MONDO:0011523	Bardet-Biedl syndrome 6
MONDO:0011504	NDE1-related microhydranencephaly
MONDO:0011503	cortisone reductase deficiency 1
MONDO:0011506	familial infantile myoclonic epilepsy
MONDO:0011505	familial hypobetalipoproteinemia 2
MONDO:0011508	lymphoma, non-Hodgkin, familial
MONDO:0011507	diabetes mellitus, congenital autoimmune
MONDO:0011509	low density lipoprotein cholesterol, mild elevation of
MONDO:0011511	clavicular hypoplasia, zygomatic arch hypoplasia, and micrognathia
MONDO:0011510	Bohring-Opitz syndrome
MONDO:0011513	Alzheimer disease, familial early-onset, with coexisting amyloid and prion pathology
MONDO:0011512	Brooke-Spiegler syndrome
MONDO:0011500	Becker nevus syndrome
MONDO:0011502	Wolfram syndrome 2
MONDO:0011501	wormian bone-multiple fractures-dentinogenesis imperfecta-skeletal dysplasia
MONDO:0060578	neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures
MONDO:0060577	neurodevelopmental disorder with microcephaly, ataxia, and seizures
MONDO:0060583	platelet abnormalities with eosinophilia and immune-mediated inflammatory disease
MONDO:0060582	auditory neuropathy-optic atrophy syndrome
MONDO:0060568	Pilarowski-Bjornsson syndrome
MONDO:0060564	HELIX syndrome
MONDO:0060596	neurodevelopmental disorder with dysmorphic facies and distal limb anomalies
MONDO:0060589	facial palsy, congenital, with ptosis and velopharyngeal dysfunction
MONDO:0060585	neuronopathy, distal hereditary motor, type 9
MONDO:0060593	actn3 deficiency
MONDO:0060592	Sweeney-Cox syndrome
MONDO:0060591	immunodeficiency, developmental delay, and hypohomocysteinemia
MONDO:0060533	microcephaly, short stature, and limb abnormalities
MONDO:0060532	congenital heart defects and skeletal malformations syndrome
MONDO:0060527	maleylacetoacetate isomerase deficiency
MONDO:0060556	joint laxity, short stature, and myopia
MONDO:0060555	vertebral, cardiac, renal, and limb defects syndrome 2
MONDO:0060554	vertebral, cardiac, renal, and limb defects syndrome 1
MONDO:0060562	encephalopathy, neonatal severe, with lactic acidosis and brain abnormalities
MONDO:0060549	congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay
MONDO:0060551	cerebellar atrophy, developmental delay, and seizures
MONDO:0060550	polydactyly, postaxial, type a7
MONDO:0011449	Salla disease
MONDO:0011448	PPARG-related familial partial lipodystrophy
MONDO:0011452	hypotrichosis 7
MONDO:0011451	cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 1
MONDO:0011454	patent ductus arteriosus-bicuspid aortic valve-hand anomalies syndrome
MONDO:0011453	ulnar ray dysgenesis with postaxial polydactyly and renal cystic dysplasia
MONDO:0011456	nephronophthisis 3
MONDO:0011455	lissencephaly, familial, with cleft palate and cerebellar hypoplasia
MONDO:0011458	Leber congenital amaurosis 4
MONDO:0011457	ataxia-telangiectasia-like disorder
MONDO:0011450	breast-ovarian cancer, familial, susceptibility to, 1
MONDO:0011438	acne
MONDO:0011437	microcephaly 4, primary, autosomal recessive
MONDO:0011439	spinocerebellar ataxia type 12
MONDO:0011441	complex regional pain syndrome type 1
MONDO:0011440	hypertension, essential, susceptibility to, 2
MONDO:0011443	febrile seizures, familial, 4
MONDO:0011442	advanced sleep phase syndrome 1
MONDO:0011445	hereditary spastic paraplegia 11
MONDO:0011444	Duane retraction syndrome 2
MONDO:0011447	epilepsy, familial focal, with variable foci
MONDO:0011446	myoclonic epilepsy, congenital deafness, macular dystrophy, and psychiatric disorders
MONDO:0023419	hyperprolinemia
MONDO:0023415	congenital candidiasis
MONDO:0011427	Ascaris lumbricoides infection, susceptibility to
MONDO:0011426	aceruloplasminemia
MONDO:0011429	juvenile idiopathic arthritis
MONDO:0011428	ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3
MONDO:0011430	pulverulent cataract
MONDO:0011432	blepharophimosis - intellectual disability syndrome, Verloes type
MONDO:0011431	MASS syndrome
MONDO:0011434	psoriasis 5, susceptibility to
MONDO:0011433	anemia, congenital hypoplastic, with multiple congenital anomalies/intellectual disability syndrome
MONDO:0011436	autosomal recessive distal spinal muscular atrophy 1
MONDO:0011435	microcephaly 2, primary, autosomal recessive, with or without cortical malformations
MONDO:0011416	generalized epilepsy with febrile seizures plus, type 1
MONDO:0011415	Leber congenital amaurosis 3
MONDO:0011418	dyslexia, susceptibility to, 3
MONDO:0011417	hemochromatosis type 3
MONDO:0011419	camera-Marugo-Cohen syndrome
MONDO:0011421	mitochondrial complex V (ATP synthase) deficiency, nuclear type 1
MONDO:0011420	short stature due to partial GHR deficiency
MONDO:0011423	autosomal recessive limb-girdle muscular dystrophy type 2E
MONDO:0011422	autosomal recessive proximal renal tubular acidosis
MONDO:0011425	dilated cardiomyopathy 1H
MONDO:0011424	Carney triad
MONDO:0023472	chondrodysplasia situs inversus imperforate anus polydactyly
MONDO:0011496	mild spondyloepiphyseal dysplasia due to COL2A1 mutation with early-onset osteoarthritis
MONDO:0011495	Langerhans-cell histiocytosis
MONDO:0011498	schizophrenia 9
MONDO:0011497	hereditary North American Indian childhood cirrhosis
MONDO:0011499	Okamoto syndrome
MONDO:0011490	diffuse panbronchiolitis
MONDO:0011492	mandibulofacial dysostosis syndrome, Bauru type
MONDO:0011491	epilepsy, idiopathic generalized, susceptibility to, 7
MONDO:0011494	hyaluronan metabolism, defect 1N
MONDO:0011493	Stickler syndrome type 2
MONDO:0011485	autosomal recessive congenital ichthyosis 5
MONDO:0011484	catecholaminergic polymorphic ventricular tachycardia 1
MONDO:0011487	Huntington disease-like 3
MONDO:0011486	congenital muscular dystrophy 1B
MONDO:0011489	hereditary spastic paraplegia 12
MONDO:0011488	microcephaly 3, primary, autosomal recessive
MONDO:0011481	craniosynostosis 2
MONDO:0011480	autosomal dominant nonsyndromic deafness 20
MONDO:0011483	polycystic bone disease
MONDO:0011482	dilated cardiomyopathy 1I
MONDO:0011474	progressive familial heart block type IB
MONDO:0011473	Leber congenital amaurosis 5
MONDO:0011476	MHC class I deficiency
MONDO:0011475	Charcot-Marie-Tooth disease type 4B2
MONDO:0011478	growth and developintellectual disability, ocular ptosis, cardiac defect, and anal atresia
MONDO:0011477	tooth agenesis, selective, 3
MONDO:0011479	postural orthostatic tachycardia syndrome
MONDO:0011470	hyperlipidemia, combined, 2
MONDO:0011472	epidermolysis bullosa simplex due to plakophilin deficiency
MONDO:0011471	inflammatory bowel disease 3
MONDO:0011459	arrhythmogenic right ventricular dysplasia 5
MONDO:0011463	polyneuropathy, lethal neonatal, axonal sensorimotor, autosomal recessive
MONDO:0011462	pyogenic arthritis-pyoderma gangrenosum-acne syndrome
MONDO:0011465	infundibulocystic basal cell carcinoma
MONDO:0011464	spinocerebellar ataxia type 11
MONDO:0011467	human herpesvirus type 6, integrated
MONDO:0011466	distal myopathy, Welander type
MONDO:0011469	congenital amegakaryocytic thrombocytopenia
MONDO:0011468	hereditary motor and sensory neuropathy, Okinawa type
MONDO:0011461	generalized epilepsy with febrile seizures plus, type 2
MONDO:0011460	arrhythmogenic right ventricular dysplasia 6
MONDO:0011405	poikiloderma with neutropenia
MONDO:0011404	Caronte
MONDO:0011407	facial paresis, hereditary congenital, 2
MONDO:0011406	cholesteatoma, congenital
MONDO:0011409	hepatic fibrosis, severe, susceptibility to, due to Schistosoma mansoni infection
MONDO:0011408	hereditary spastic paraplegia 10
MONDO:0011410	Hirschsprung disease with heart defects, laryngeal anomalies, and preaxial polydactyly
MONDO:0011412	familial encephalopathy with neuroserpin inclusion bodies
MONDO:0011411	Chudley-McCullough syndrome
MONDO:0011414	Peters anomaly
MONDO:0011413	cataract 9 multiple types
MONDO:0011401	Alzheimer disease without neurofibrillary tangles
MONDO:0011400	dilated cardiomyopathy 1G
MONDO:0011403	left ventricular noncompaction 1
MONDO:0011402	congenital cataracts-facial dysmorphism-neuropathy syndrome
MONDO:0060489	46,XX sex reversal 4
MONDO:0060486	arthrogryposis multiplex congenita 1, neurogenic, with myelin defect
MONDO:0060496	neurodevelopmental disorder with hypotonia, neuropathy, and deafness
MONDO:0060491	neurodevelopmental disorder with involuntary movements
MONDO:0060490	neurodevelopmental disorder with microcephaly, hypotonia, and variable brain anomalies
MONDO:0060457	autoinflammation with arthritis and dyskeratosis
MONDO:0060456	cerebral sclerosis, diffuse, scholz type
MONDO:0060455	X-linked congenital hemolytic anemia
MONDO:0023483	infectious myositis
MONDO:0023310	hemiplegic migraine
MONDO:0011328	autosomal dominant limb-girdle muscular dystrophy type 1E
MONDO:0011327	neuronal intranuclear inclusion disease
MONDO:0013989	developmental and epileptic encephalopathy, 14
MONDO:0011329	cerebral palsy, spastic quadriplegic, 1
MONDO:0011331	congenital chylothorax
MONDO:0013994	Joubert syndrome 20
MONDO:0013995	cholestasis, intrahepatic, of pregnancy, 3
MONDO:0011330	spinocerebellar ataxia type 10
MONDO:0013992	obesity due to leptin receptor gene deficiency
MONDO:0011333	light fixation seizure syndrome
MONDO:0013993	pontocerebellar hypoplasia type 7
MONDO:0011332	Dyserythropoiesis, congenital, with ultrastructurally normal erythroblast heterochromatin
MONDO:0011335	spondyloepimetaphyseal dysplasia with multiple dislocations
MONDO:0013998	MEGF8-related Carpenter syndrome
MONDO:0013999	optic nerve edema-splenomegaly syndrome
MONDO:0011334	limb-mammary syndrome
MONDO:0011337	familial hemophagocytic lymphohistiocytosis 2
MONDO:0013996	focal facial dermal dysplasia type II
MONDO:0011336	familial hemophagocytic lymphohistiocytosis 4
MONDO:0013997	focal facial dermal dysplasia type IV
MONDO:0001999	primary pulmonary hypertension
MONDO:0013990	pontocerebellar hypoplasia type 8
MONDO:0013991	obesity due to congenital leptin deficiency
MONDO:0023303	Hamanishi-Ueba-Tsuji syndrome
MONDO:0023305	heavy metal poisoning
MONDO:0011317	microcephaly, severe, with skeletal anomalies including posterior rib-Gap defects
MONDO:0011316	osteosclerotic chondrodysplasia, lethal, with intracellular inclusions
MONDO:0013978	autosomal recessive nonsyndromic deafness 70
MONDO:0011319	activator of liver function 1
MONDO:0013979	primary ciliary dyskinesia 19
MONDO:0011318	Tonoki syndrome
MONDO:0013983	ectodermal dysplasia 11B, hypohidrotic/hair/tooth type, autosomal recessive
MONDO:0011320	radioulnar synostosis-microcephaly-scoliosis syndrome
MONDO:0013984	autosomal recessive nonsyndromic deafness 84B
MONDO:0013981	myoclonus, familial
MONDO:0011322	Oroacral syndrome, Verloes-Koulischer type
MONDO:0013982	ectodermal dysplasia 11A, hypohidrotic/hair/tooth type, autosomal dominant
MONDO:0011321	expansile bone lesions
MONDO:0013987	combined oxidative phosphorylation defect type 15
MONDO:0011324	hypospadias, hypertelorism, upper 51D coloboma, and mixed-type hearing loss
MONDO:0011323	arhinia, choanal atresia, and microphthalmia
MONDO:0013988	congenital heart defects, multiple types, 3
MONDO:0013985	autosomal recessive nonsyndromic deafness 18B
MONDO:0011326	citrullinemia, type II, adult-onset
MONDO:0013986	combined oxidative phosphorylation defect type 14
MONDO:0011325	Fanconi anemia complementation group F
MONDO:0013980	palmoplantar keratoderma, punctate type ib
MONDO:0001983	peripheral degeneration of cornea
MONDO:0001982	Niemann-Pick disease
MONDO:0001981	cholesterol ester storage disease
MONDO:0001980	Wolman disease
MONDO:0001987	senile degeneration of brain
MONDO:0001986	Argyll Robertson pupil
MONDO:0001985	partial arterial retinal occlusion
MONDO:0025956	ovarian remnant syndrome
MONDO:0001984	candidal paronychia
MONDO:0013969	combined oxidative phosphorylation defect type 11
MONDO:0011306	muscular dystrophy, congenital, with cerebellar atrophy
MONDO:0011305	cerebral cavernous malformation 3
MONDO:0011308	gracile syndrome
MONDO:0013967	peroxisome biogenesis disorder 14B
MONDO:0013968	PGM1-CDG
MONDO:0011307	schizophrenia 2
MONDO:0011309	familial gestational hyperthyroidism
MONDO:0013972	Perrault syndrome 2
MONDO:0013973	ectodermal dysplasia 5, hair/nail type
MONDO:0011311	glaucoma 1, open angle, F
MONDO:0013970	branched-chain keto acid dehydrogenase kinase deficiency
MONDO:0013971	leukoencephalopathy-thalamus and brainstem anomalies-high lactate syndrome
MONDO:0011310	long chain fatty acids, defect in transport of
MONDO:0011313	megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 1
MONDO:0013976	ectodermal dysplasia 9, hair/nail type
MONDO:0013977	combined oxidative phosphorylation defect type 13
MONDO:0011312	thyroid carcinoma, nonmedullary, with or without cell oxyphilia
MONDO:0013974	ectodermal dysplasia 6, hair/nail type
MONDO:0011315	Osebold skeletal dysplasia/osteolysis syndrome
MONDO:0011314	Graves disease, susceptibility to, 2
MONDO:0013975	ectodermal dysplasia 7, hair/nail type
MONDO:0001979	dumping syndrome
MONDO:0001978	regional ureteric cancer
MONDO:0001977	ureteral lymphoma
MONDO:0001994	sphenoidal sinus cancer
MONDO:0001993	seminal vesicle adenocarcinoma
MONDO:0001992	rete testis adenocarcinoma
MONDO:0001991	malignant cardiac germ cell tumor
MONDO:0001998	Foster-Kennedy syndrome
MONDO:0001997	root resorption
MONDO:0001996	steroid-induced glaucoma - borderline
MONDO:0001995	sphenoid sinus squamous cell carcinoma
MONDO:0013958	monocyte and dendritic cell deficiency, autosomal recessive
MONDO:0013959	Charcot-Marie-Tooth disease type 4F
MONDO:0013956	mendelian susceptibility to mycobacterial diseases due to partial STAT1 deficiency
MONDO:0013957	mendelian susceptibility to mycobacterial diseases due to partial IRF8 deficiency
MONDO:0001990	malignant cardiac peripheral nerve sheath neoplasm
MONDO:0013961	hypogonadotropic hypogonadism 16 with or without anosmia
MONDO:0013962	hereditary spastic paraplegia 53
MONDO:0011300	myopia 3, autosomal dominant
MONDO:0013960	sinoatrial node dysfunction and deafness
MONDO:0013965	lethal congenital contracture syndrome 4
MONDO:0011302	type 1 diabetes mellitus 17
MONDO:0011301	pseudohypoparathyroidism type 1B
MONDO:0013966	catecholaminergic polymorphic ventricular tachycardia 4
MONDO:0013963	autosomal recessive nonsyndromic deafness 93
MONDO:0011304	cerebral cavernous malformation 2
MONDO:0011303	focal segmental glomerulosclerosis 1
MONDO:0013964	Diamond-Blackfan anemia 11
MONDO:0001989	atrophic glossitis
MONDO:0001988	external pathological resorption
MONDO:0011375	brittle bone disorder
MONDO:0011374	hypercholesterolemia, familial, 4
MONDO:0011377	long QT syndrome 3
MONDO:0011376	ventricular fibrillation, paroxysmal familial, type 1
MONDO:0011379	medullary cystic kidney disease 2
MONDO:0011378	CFM1
MONDO:0011371	hydroa vacciniforme, familial
MONDO:0011370	Stargardt disease 4
MONDO:0011373	urinary tract infections, recurrent, susceptibility to
MONDO:0011372	microcephaly with simplified gyral pattern
MONDO:0011364	autosomal recessive nonsyndromic deafness 16
MONDO:0011363	diabetes mellitus, noninsulin-dependent, 3
MONDO:0011366	ovarian germ cell tumor
MONDO:0011365	blepharophimosis - intellectual disability syndrome, SBBYS type
MONDO:0011368	papillary thyroid Microcarcinoma
MONDO:0011367	Acrodysplasia with ossification abnormalities, short stature, and fibular hypoplasia
MONDO:0011369	hypercholesterolemia, autosomal dominant, 3
MONDO:0011360	autosomal recessive nonsyndromic deafness 14
MONDO:0011362	myopathy, myofibrillar, 9, with early respiratory failure
MONDO:0011361	prostate cancer/brain cancer susceptibility
MONDO:0011349	osteoma of cranial vault, familial
MONDO:0037937	pyrimidine metabolism disease
MONDO:0037938	inborn disorder of aspartate family metabolism
MONDO:0037939	porphyria
MONDO:0011353	atrial septal defect, secundum, with various cardiac and Noncardiac defects
MONDO:0037940	inherited auditory system disease
MONDO:0011352	neuroendocrine carcinoma of salivary glands, sensorineural hearing loss, and enamel hypoplasia
MONDO:0011355	cone-rod dystrophy 7
MONDO:0011354	situs inversus totalis with cystic dysplasia of kidneys and pancreas
MONDO:0011357	eccrine syringofibroadenomatosis with eyelid abnormalities
MONDO:0011356	exostosis, Dupuytren subungual
MONDO:0011359	acromelic frontonasal dysostosis
MONDO:0011358	blue nevi, familial multiple
MONDO:0011351	autosomal recessive nonsyndromic deafness 21
MONDO:0011350	autosomal dominant nonsyndromic deafness 17
MONDO:0025986	megacystis-microcolon-intestinal hypoperistalsis syndrome
MONDO:0011339	hereditary spastic paraplegia 8
MONDO:0011338	Omenn syndrome
MONDO:0011342	SLC35A1-CDG
MONDO:0011341	microcephaly, facial abnormalities, micromelia, and intellectual disability
MONDO:0011344	parotitis, juvenile recurrent
MONDO:0011343	follicular atrophoderma, perioral pigmented, with milia and epidermoid cysts
MONDO:0011346	xanthinuria type II
MONDO:0011345	facial dysmorphism, selective tooth agenesis, and choroid calcification
MONDO:0011348	non-syndromic polydactyly
MONDO:0011347	craniosynostosis with ectopia lentis
MONDO:0011340	congenital tracheal stenosis
MONDO:0013909	human herpesvirus 8, susceptibility to
MONDO:0001921	chronic atticoantral disease
MONDO:0001920	chronic purulent otitis media
MONDO:0013903	nystagmus 7, congenital, autosomal dominant
MONDO:0013904	muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 8
MONDO:0013901	spermatogenic failure 10
MONDO:0013902	aortic valve disease 2
MONDO:0013907	bilateral generalized polymicrogyria
MONDO:0013908	thyrotoxic periodic paralysis, susceptibility to, 3
MONDO:0013905	autosomal recessive spinocerebellar ataxia 13
MONDO:0013906	amelogenesis imperfecta hypomaturation type 2A4
MONDO:0001919	cystoid macular retinal degeneration
MONDO:0013910	hypogonadotropic hypogonadism 8 with or without anosmia
MONDO:0013911	hypogonadotropic hypogonadism 9 with or without anosmia
MONDO:0001914	scleromalacia perforans
MONDO:0001913	oligospermia
MONDO:0001912	acute frontal sinusitis
MONDO:0001911	tracheal calcification
MONDO:0001918	epiphora due to excess lacrimation
MONDO:0001917	chronic perichondritis of pinna
MONDO:0001916	gastrointestinal tularemia
MONDO:0001915	orbital cyst
MONDO:0001932	atrophic vulva
MONDO:0001931	pericholangitis
MONDO:0001930	acute cholangitis
MONDO:0013900	alternating hemiplegia of childhood 2
MONDO:0001925	retinal dystrophy in systemic or cerebroretinal lipidoses
MONDO:0001924	dystrophies primarily involving the retinal pigment epithelium
MONDO:0001923	vitreoretinal dystrophy
MONDO:0001922	pyoureter
MONDO:0001929	ascending cholangitis
MONDO:0001928	suppurative cholangitis
MONDO:0001927	pulmonary valve insufficiency
MONDO:0001926	ureteral disease
MONDO:0001910	ochronosis disorder
MONDO:0001909	renal tubular acidosis
MONDO:0001908	hypophosphatasia
MONDO:0001903	calcific tendinitis
MONDO:0001902	congenital agammaglobulinemia
MONDO:0001901	selective IgG subclass deficiency
MONDO:0001900	central neurocytoma
MONDO:0001907	adult dermatomyositis
MONDO:0001906	posterior dislocation of lens
MONDO:0001905	bicipital tenosynovitis
MONDO:0001904	polyneuropathy due to drug
MONDO:0001961	glossopharyngeal neuralgia
MONDO:0001960	Alpers syndrome
MONDO:0001965	sclerosing keratitis
MONDO:0001964	chronic tubotympanic suppurative otitis media
MONDO:0001963	cerebral degeneration disease
MONDO:0001962	abnormality of glucagon secretion
MONDO:0013947	young adult-onset distal hereditary motor neuropathy
MONDO:0013948	peroxisome biogenesis disorder 10A (Zellweger)
MONDO:0013945	peroxisome biogenesis disorder 9B
MONDO:0013946	hypogonadotropic hypogonadism 15 with or without anosmia
MONDO:0013949	peroxisome biogenesis disorder 11A (Zellweger)
MONDO:0013950	peroxisome biogenesis disorder 11B
MONDO:0013951	peroxisome biogenesis disorder 12A (Zellweger)
MONDO:0013954	mendelian susceptibility to mycobacterial diseases due to complete IL12B deficiency
MONDO:0013955	mendelian susceptibility to mycobacterial diseases due to complete IL12RB1 deficiency
MONDO:0013952	peroxisome biogenesis disorder 13A (Zellweger)
MONDO:0013953	immunodeficiency 28
MONDO:0001958	autosomal dominant cerebellar ataxia
MONDO:0001957	critical illness polyneuropathy
MONDO:0001956	capillary leak syndrome
MONDO:0001955	protozoal dysentery
MONDO:0001959	labyrinthine bilateral reactive loss
MONDO:0001972	Brucella melitensis brucellosis
MONDO:0001971	farmer's lung disease
MONDO:0001970	hypokalemic periodic paralysis
MONDO:0001976	chorea gravidarum
MONDO:0001975	cavernous hemangioma of orbit
MONDO:0001974	hemangioma of orbit
MONDO:0001973	Brucella abortus brucellosis
MONDO:0013936	peroxisome biogenesis disorder 6A (Zellweger)
MONDO:0013937	peroxisome biogenesis disorder 6B
MONDO:0013934	combined immunodeficiency due to STK4 deficiency
MONDO:0013935	Usher syndrome type 1J
MONDO:0013938	peroxisome biogenesis disorder 7A (Zellweger)
MONDO:0013939	peroxisome biogenesis disorder 7B
MONDO:0013940	primary ciliary dyskinesia 18
MONDO:0013943	peroxisome biogenesis disorder 8B
MONDO:0013944	autoinflammation-PLCG2-associated antibody deficiency-immune dysregulation
MONDO:0013941	metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria
MONDO:0013942	peroxisome biogenesis disorder 8A (Zellweger)
MONDO:0001969	mixed gonadal dysgenesis
MONDO:0001968	46 XY gonadal dysgenesis
MONDO:0001967	gonadal dysgenesis
MONDO:0001966	chronic closed-angle glaucoma
MONDO:0001943	Plasmodium malariae malaria
MONDO:0001942	generalized anxiety disorder
MONDO:0001941	blindness (disorder)
MONDO:0001940	pleuropneumonia
MONDO:0013925	methylmalonic acidemia with homocystinuria, type cblJ
MONDO:0013926	hypogonadotropic hypogonadism 14 with or without anosmia
MONDO:0013923	microcephaly 9, primary, autosomal recessive
MONDO:0013924	osteogenesis imperfecta type 13
MONDO:0013929	autosomal recessive nonsyndromic deafness 98
MONDO:0013927	peroxisome biogenesis disorder 3A (Zellweger)
MONDO:0013928	dystonia 23
MONDO:0013932	peroxisome biogenesis disorder 5A (Zellweger)
MONDO:0013933	peroxisome biogenesis disorder 5B
MONDO:0013930	peroxisome biogenesis disorder 4A (Zellweger)
MONDO:0013931	peroxisome biogenesis disorder 4B
MONDO:0001936	brawny scleritis
MONDO:0001935	neurogenic arthropathy
MONDO:0001934	primary hypertrophic osteoarthropathy
MONDO:0001933	endocrine pancreas disease
MONDO:0001939	skin epithelioid hemangioma
MONDO:0001938	vulvar dystrophy
MONDO:0001937	LEOPARD syndrome
MONDO:0001950	corneal ectasia
MONDO:0001954	thrombophlebitis migrans
MONDO:0001953	pyuria
MONDO:0001952	parietal lobe cancer
MONDO:0001951	Norwegian scabies
MONDO:0013914	hypogonadotropic hypogonadism 12 with or without anosmia
MONDO:0013915	hypogonadotropic hypogonadism 13 with or without anosmia
MONDO:0013912	hypogonadotropic hypogonadism 10 with or without anosmia
MONDO:0013913	hypogonadotropic hypogonadism 11 with or without anosmia
MONDO:0013918	distal tetrasomy 15q
MONDO:0013919	epilepsy, idiopathic generalized, susceptibility to, 12
MONDO:0013916	nephronophthisis 14
MONDO:0013917	nephronophthisis 15
MONDO:0013921	herpes simplex encephalitis, susceptibility to, 4
MONDO:0013922	Seckel syndrome 7
MONDO:0013920	herpes simplex encephalitis, susceptibility to, 3
MONDO:0001947	suppurative thyroiditis
MONDO:0001946	hyperestrogenism
MONDO:0001945	postencephalitic Parkinson disease
MONDO:0001944	mixed malaria
MONDO:0001949	acute thyroiditis
MONDO:0001948	Riedel's fibrosing thyroiditis
MONDO:0023388	pityriasis rotunda
MONDO:0035398	hypomyelination of early myelinating structures
MONDO:0023370	neoplastic disease or syndrome
MONDO:0011397	autosomal dominant cerebellar ataxia, deafness and narcolepsy
MONDO:0011396	keratoderma hereditarium mutilans with ichthyosis
MONDO:0011399	alpha thalassemia
MONDO:0011398	dystrophic epidermolysis bullosa pruriginosa
MONDO:0011391	megalencephalic leukoencephalopathy with subcortical cysts
MONDO:0011390	focal segmental glomerulosclerosis 2
MONDO:0011393	hypoalphalipoproteinemia, primary, 1
MONDO:0011392	autosomal recessive nonsyndromic deafness 20
MONDO:0011395	cone-rod dystrophy 3
MONDO:0011394	keratosis pilaris atrophicans
MONDO:0023368	Ho-Kaufman-McAlister syndrome
MONDO:0023369	disease of facial skeleton
MONDO:0011386	microvascular complications of diabetes, susceptibility to, 1
MONDO:0011385	intervertebral disc degenerative disorder
MONDO:0011388	cervical cancer
MONDO:0011387	psoriasis 4, susceptibility to
MONDO:0011389	autosomal dominant nonsyndromic deafness 16
MONDO:0011380	leukoencephalopathy with vanishing white matter
MONDO:0011382	sickle cell anemia
MONDO:0011381	dominant beta-thalassemia
MONDO:0011384	hypertension, essential, susceptibility to, 1
MONDO:0011383	autoimmune lymphoproliferative syndrome type 2A
MONDO:0035349	localized dystrophic epidermolysis bullosa
MONDO:0035357	portosinusoidal vascular disease
MONDO:0035354	IgG4-related systemic disease
MONDO:0035363	IRF2BPL-related regressive neurodevelopmental disorder-dystonia-seizures syndrome
MONDO:0035362	TRIM22-related inflammatory bowel disease
MONDO:0035369	MTHFS-related developmental delay-microcephaly-short stature-epilepsy syndrome
MONDO:0035375	multisystem inflammatory syndrome in children and adults
MONDO:0035370	ALPI-related inflammatory bowel disease
MONDO:0001884	abducens nerve neoplasm
MONDO:0001883	blue toe syndrome
MONDO:0001882	bacteriuria
MONDO:0001881	toxic shock syndrome
MONDO:0001888	anus lymphoma
MONDO:0001887	Allen-Masters syndrome
MONDO:0001886	midline cystocele
MONDO:0001885	lateral cystocele
MONDO:0011207	xanthomatosis, susceptibility to
MONDO:0011206	ventriculomegaly with defects of the radius and kidney
MONDO:0013868	porokeratosis 7, disseminated superficial actinic type
MONDO:0011209	progeroid facial appearance with hand anomalies
MONDO:0013869	adenine phosphoribosyltransferase deficiency
MONDO:0011208	malignant atrophic papulosis
MONDO:0001880	median rhomboid glossitis
MONDO:0013873	IMAGe syndrome
MONDO:0011210	mitochondrial intermembrane space protein Tim12, yeast, homolog of
MONDO:0013874	glucocorticoid deficiency 4
MONDO:0013871	Seckel syndrome 6
MONDO:0011212	sensorineural hearing loss, retinal pigment epithelium lesions, discolored teeth
MONDO:0011211	axial spondylometaphyseal dysplasia
MONDO:0013872	prostate cancer, hereditary, 2
MONDO:0011214	progressive familial intrahepatic cholestasis type 3
MONDO:0013877	mitochondrial pyruvate carrier deficiency
MONDO:0013878	pulmonary fibrosis and/or bone marrow failure, Telomere-related, 1
MONDO:0011213	Pierpont syndrome
MONDO:0011216	hemochromatosis type 2A
MONDO:0013875	3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome
MONDO:0011215	osteocraniostenosis
MONDO:0037847	vertebral joint disease
MONDO:0013876	basal cell carcinoma, susceptibility to, 7
MONDO:0001879	anus cancer
MONDO:0001878	acquired hypertrophic pyloric stenosis
MONDO:0013870	TMEM165-CDG
MONDO:0001895	acute retrobulbar neuritis
MONDO:0001894	spinal cord sarcoma
MONDO:0001893	spinal cord melanoma
MONDO:0001892	spinal cord lymphoma
MONDO:0001899	rheumatic congestive heart failure
MONDO:0001898	optic choroid disease
MONDO:0001897	bilateral hyperactive labyrinth
MONDO:0001896	obstructive hydrocephalus
MONDO:0013859	cataract 38
MONDO:0013857	alar cleft, isolated
MONDO:0013858	pontine tegmental cap dysplasia
MONDO:0001891	malignant anus melanoma
MONDO:0001890	pulp erosion
MONDO:0013862	immunodeficiency, common variable, 7
MONDO:0013863	combined immunodeficiency due to LRBA deficiency
MONDO:0011201	tremor, hereditary essential, 2
MONDO:0013860	idiopathic membranous glomerulonephritis
MONDO:0011200	torsion dystonia 7
MONDO:0013861	amyotrophic lateral sclerosis type 17
MONDO:0011203	Pierre Robin sequence with pectus excavatum and rib and scapular anomalies
MONDO:0013866	neuronal ceroid lipofuscinosis 11
MONDO:0013867	brown-Vialetto-van Laere syndrome 2
MONDO:0011202	RHYNS syndrome
MONDO:0011205	medium chain 3-ketoacyl-Coa thiolase deficiency
MONDO:0013864	Cornelia de Lange syndrome 4
MONDO:0013865	mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency
MONDO:0037858	inherited fatty acid metabolism disorder
MONDO:0011204	cerebellar degeneration-related autoantigen 3
MONDO:0001889	ovarian dysfunction
MONDO:0001862	malignant visceral pleura tumor
MONDO:0001861	malignant parietal pleura tumor
MONDO:0001860	folic acid deficiency anemia
MONDO:0001866	bipolar I disorder
MONDO:0001865	autoimmune polyendocrinopathy syndrome
MONDO:0001864	residual stage angle-closure glaucoma
MONDO:0001863	aorta atresia
MONDO:0013848	dilated cardiomyopathy 2B
MONDO:0013849	microcephaly 8, primary, autosomal recessive
MONDO:0013846	peripartum cardiomyopathy, susceptibility to
MONDO:0013847	chromosome 16p11.2 duplication syndrome
MONDO:0013851	autosomal dominant aplasia and myelodysplasia
MONDO:0013852	hypertrophic cardiomyopathy 21
MONDO:0013850	periodic fever, menstrual cycle-dependent
MONDO:0013855	influenza, severe, susceptibility to
MONDO:0013856	hypertelorism and other facial dysmorphism, brachydactyly, genital abnormalities, intellectual disability, and recurrent inflammatory episodes
MONDO:0013853	pontocerebellar hypoplasia type 1B
MONDO:0013854	primary ciliary dyskinesia 17
MONDO:0001859	algoneurodystrophy
MONDO:0001858	Tietze syndrome
MONDO:0001857	Brucella canis brucellosis
MONDO:0001856	splenic artery aneurysm
MONDO:0001873	geniculate ganglionitis
MONDO:0001872	vestibular nystagmus
MONDO:0001871	acute diffuse glomerulonephritis
MONDO:0001870	acute poststreptococcal glomerulonephritis
MONDO:0001877	infertility due to extratesticular cause
MONDO:0001876	renal artery atheroma
MONDO:0001875	epicondylitis
MONDO:0001874	toxic labyrinthitis
MONDO:0013837	deafness-encephaloneuropathy-obesity-valvulopathy syndrome
MONDO:0013838	coenzyme Q10 deficiency, primary, 3
MONDO:0013835	muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 7
MONDO:0013836	familial steroid-resistant nephrotic syndrome with sensorineural deafness
MONDO:0013839	hereditary sensory and autonomic neuropathy type 6
MONDO:0013840	encephalopathy-hypertrophic cardiomyopathy-renal tubular disease syndrome
MONDO:0013841	stuttering, familial persistent, 3
MONDO:0013844	stuttering, familial persistent, 4
MONDO:0013845	auriculocondylar syndrome 2
MONDO:0013842	cortisone reductase deficiency 2
MONDO:0013843	intestinal obstruction in the newborn due to guanylate cyclase 2C deficiency
MONDO:0001869	paraurethral gland cancer
MONDO:0001868	primary angle-closure glaucoma
MONDO:0001867	phaeohyphomycosis
MONDO:0037870	valine metabolism disease
MONDO:0037871	amino acid metabolism disease
MONDO:0037872	bordetellosis
MONDO:0023232	giant cell myocarditis
MONDO:0023235	giant congenital nevus
MONDO:0023238	giant mammary hamartoma
MONDO:0023230	Ghose-Sachdev-Kumar syndrome
MONDO:0011254	brachydactyly, intraventricular septal defect, and deafness
MONDO:0011253	craniomicromelic syndrome
MONDO:0011256	emphysema, congenital, with deafness, penoscrotal web, and intellectual disability
MONDO:0011255	mandibulofacial dysostosis-macroblepharon-macrostomia syndrome
MONDO:0011258	branchiootic syndrome 1
MONDO:0011257	MPI-CDG
MONDO:0011259	retinitis pigmentosa 22
MONDO:0011250	microcephaly, macrotia, and intellectual disability
MONDO:0011252	spondyloepimetaphyseal dysplasia, Shohat type
MONDO:0011251	facial dysmorphism, cleft palate, hearing loss, and camptodactyly
MONDO:0023221	Gaucher ichthyosis restrictive dermopathy
MONDO:0023224	inherited reflex epilepsy
MONDO:0023226	gershinibaruch Leibo syndrome
MONDO:0023227	gestational diabetes insipidus
MONDO:0011239	colobomatous macrophthalmia-microcornea syndrome
MONDO:0037807	glycerol metabolism disease
MONDO:0011243	grange syndrome
MONDO:0011242	Bartter disease type 4a
MONDO:0011245	ichthyosis, hystrix-like, with deafness
MONDO:0011244	Marshall-Smith syndrome
MONDO:0011247	jejunal atresia with renal adysplasia
MONDO:0011246	megaconial type congenital muscular dystrophy
MONDO:0011249	torsion dystonia with onset in infancy
MONDO:0011248	distal monosomy 13q
MONDO:0011241	pseudoacromegaly with severe insulin resistance
MONDO:0011240	megalencephaly-capillary malformation-polymicrogyria syndrome
MONDO:0023212	Garret-Tripp syndrome
MONDO:0023214	gas bloat syndrome
MONDO:0023217	gastro-enteropancreatic neuroendocrine tumor
MONDO:0011229	ethylmalonic encephalopathy
MONDO:0011228	creases, infra-auricular cutaneous, with tall stature and advanced bone age
MONDO:0011232	migraine, familial hemiplegic, 2
MONDO:0013895	Adams-Oliver syndrome 3
MONDO:0011231	febrile seizures, familial, 2
MONDO:0013896	Joubert syndrome 18
MONDO:0013893	multiple sclerosis, susceptibility to, 5
MONDO:0011234	auriculocondylar syndrome 1
MONDO:0037821	porphyrin metabolism disease
MONDO:0011233	Axenfeld-Rieger syndrome type 3
MONDO:0013894	short stature-onychodysplasia-facial dysmorphism-hypotrichosis syndrome
MONDO:0011236	hyperinsulinism due to glucokinase deficiency
MONDO:0013899	Weill-Marchesani syndrome 3
MONDO:0011235	pelvic dysplasia-arthrogryposis of lower limbs syndrome
MONDO:0013897	Loeys-Dietz syndrome 4
MONDO:0011238	chondrodysplasia punctata, brachytelephalangic, autosomal
MONDO:0013898	karyomegalic interstitial nephritis
MONDO:0011237	hyperlipidemia, combined, 1
MONDO:0023208	Fuqua Berkovitz syndrome
MONDO:0023209	galactorrhoea-hyperprolactinaemia
MONDO:0013891	amyotrophic lateral sclerosis type 18
MONDO:0013892	C3 glomerulonephritis
MONDO:0011230	ossification of the posterior longitudinal ligament of the spine
MONDO:0013890	congenital myopathy with internal nuclei and atypical cores
MONDO:0023200	Fryns Fabry Remans syndrome
MONDO:0023201	Fryns Smeets Thiry syndrome
MONDO:0023203	Fuchs atrophia gyrata chorioideae et retinae
MONDO:0023204	Fukuda-Miyanomae-Nakata syndrome
MONDO:0023206	functional pancreatic neuroendocrine tumor
MONDO:0011218	autosomal recessive congenital ichthyosis 11
MONDO:0011217	desmosterolosis
MONDO:0013879	pulmonary fibrosis and/or bone marrow failure, Telomere-related, 2
MONDO:0037829	purine metabolism disease
MONDO:0011219	Fried's tooth and nail syndrome
MONDO:0013884	neuronopathy, distal hereditary motor, type 5B
MONDO:0011221	Weyers ulnar ray/oligodactyly syndrome
MONDO:0013885	Malan overgrowth syndrome
MONDO:0011220	parkinson disease 3, autosomal dominant
MONDO:0011223	amyotrophic lateral sclerosis type 4
MONDO:0013882	hyperphosphatasia with intellectual disability syndrome 2
MONDO:0011222	glaucoma 1, open angle, D
MONDO:0013883	congenital myasthenic syndrome 13
MONDO:0011225	severe combined immunodeficiency due to DCLRE1C deficiency
MONDO:0013888	tremor, hereditary essential, 4
MONDO:0011224	monomelic amyotrophy
MONDO:0013889	short stature-optic atrophy-Pelger-HuC+t anomaly syndrome
MONDO:0011227	short stature-auditory canal atresia-mandibular hypoplasia-skeletal anomalies syndrome
MONDO:0013886	nonprogressive cerebellar atxia with intellectual disability
MONDO:0011226	autosomal dominant nonsyndromic deafness 15
MONDO:0013887	heterotaxy, visceral, 6, autosomal
MONDO:0013880	facial paresis, hereditary congenital, 3
MONDO:0013881	congenital nephrotic syndrome - interstitial lung disease - epidermolysis bullosa syndrome
MONDO:0001800	equatorial staphyloma
MONDO:0001811	tetanic cataract
MONDO:0001810	hypoglossal nerve disease
MONDO:0001809	adhesions of uterus
MONDO:0001804	anterior scleritis
MONDO:0001803	myringitis bullosa hemorrhagica
MONDO:0001802	acute tympanitis
MONDO:0001801	staphyloma posticum
MONDO:0001808	chronic subinvolution of uterus
MONDO:0001807	familial combined hyperlipidemia
MONDO:0001806	vaginal squamous tumor
MONDO:0001805	female breast central part cancer
MONDO:0001840	schistosomiasis
MONDO:0001844	uterine corpus myxoid leiomyoma
MONDO:0001843	uterus interstitial leiomyoma
MONDO:0001842	uterine corpus dissecting leiomyoma
MONDO:0001841	uterine corpus epithelioid leiomyoma
MONDO:0013826	autosomal recessive nonsyndromic deafness 86
MONDO:0013827	hyperekplexia 3
MONDO:0013824	Joubert syndrome 17
MONDO:0013825	congenital diarrhea 6
MONDO:0013828	hyperekplexia 2
MONDO:0013829	UV-sensitive syndrome 2
MONDO:0013830	keratoconus 5
MONDO:0013833	keratoconus 7
MONDO:0013834	UV-sensitive syndrome 3
MONDO:0013831	keratoconus 6
MONDO:0013832	keratoconus 8
MONDO:0001837	acute gonococcal salpingitis
MONDO:0001836	amenorrhea
MONDO:0001835	facial paralysis
MONDO:0001834	visual pathway disease
MONDO:0001839	interstitial cystitis
MONDO:0001838	acute gonococcal prostatitis
MONDO:0001851	primary lacrimal atrophy
MONDO:0001850	female breast lower-outer quadrant cancer
MONDO:0001855	rubeosis iridis
MONDO:0001854	lacrimal apparatus disease
MONDO:0001853	contact blepharoconjunctivitis
MONDO:0001852	small intestine lymphoma
MONDO:0013815	FGFR2-related bent bone dysplasia
MONDO:0013816	palmoplantar keratoderma, mutilating, with periorificial keratotic plaques
MONDO:0013813	dystonia 21
MONDO:0013814	podoconiosis, susceptibility to
MONDO:0013819	intellectual disability, autosomal dominant 14
MONDO:0300000	SSR3-CDG
MONDO:0013817	preeclampsia/eclampsia 5
MONDO:0013818	trichohepatoenteric syndrome 2
MONDO:0013822	acrodysostosis 2 with or without hormone resistance
MONDO:0013823	autosomal dominant nonsyndromic deafness 4B
MONDO:0013820	intellectual disability, autosomal dominant 15
MONDO:0013821	intellectual disability, autosomal dominant 16
MONDO:0001848	Morgagni cataract
MONDO:0001847	nuclear senile cataract
MONDO:0001846	uterine corpus bizarre leiomyoma
MONDO:0001845	uterine corpus lipoleiomyoma
MONDO:0001849	chronic orbital inflammation
MONDO:0001822	hypolipoproteinemia
MONDO:0001821	hypoactive sexual desire disorder
MONDO:0001820	focal labyrinthitis
MONDO:0013804	intellectual disability, autosomal dominant 12
MONDO:0013805	intellectual disability, autosomal dominant 13
MONDO:0013802	infantile cerebellar-retinal degeneration
MONDO:0013803	leukoencephalopathy with calcifications and cysts
MONDO:0013808	Maffucci syndrome
MONDO:0013809	cerebellar ataxia, neuropathy, and vestibular areflexia syndrome
MONDO:0013806	familial cutaneous telangiectasia and oropharyngeal predisposition cancer syndrome
MONDO:0013807	congenital stationary night blindness 1E
MONDO:0013811	combined oxidative phosphorylation defect type 9
MONDO:0013812	Baraitser-winter syndrome 2
MONDO:0013810	COG6-CGD
MONDO:0001815	extrapyramidal and movement disease
MONDO:0001814	patent ductus arteriosus
MONDO:0001813	squamous blepharitis
MONDO:0001812	parasitic eyelid infestation
MONDO:0001819	multiple cranial nerve palsy
MONDO:0001818	facial neuralgia
MONDO:0001817	acute closed-angle glaucoma
MONDO:0001816	scleroperikeratitis
MONDO:0001833	lacrimal duct obstruction
MONDO:0001832	bacterial esophagitis
MONDO:0001831	irregular astigmatism
MONDO:0001830	somatization disorder
MONDO:0013800	Ehlers-Danlos syndrome, kyphoscoliotic and deafness type
MONDO:0013801	developmental and epileptic encephalopathy, 13
MONDO:0001826	hypobetalipoproteinemia
MONDO:0001825	squamous papilloma
MONDO:0001824	polyneuropathy
MONDO:0001823	sick sinus syndrome
MONDO:0001829	lumbosacral plexus lesion
MONDO:0001828	acquired color blindness
MONDO:0001827	white piedra
MONDO:0023272	goniodysgenesis intellectual disability short stature
MONDO:0023273	pigmented dermatofibrosarcoma protuberans
MONDO:0023275	Graham-Boyle-Troxell syndrome
MONDO:0011298	schizophrenia 8
MONDO:0011297	autosomal dominant nocturnal frontal lobe epilepsy 2
MONDO:0011299	Huntington disease-like 1
MONDO:0011290	dislocated elbows, bowed tibias, scoliosis, deafness, cataract, microcephaly, and intellectual disability
MONDO:0011292	dermatitis, atopic
MONDO:0011291	congenital disorder of glycosylation type 1C
MONDO:0011294	schizophrenia 5
MONDO:0011293	Homocysteinemia
MONDO:0011296	Meckel syndrome, type 2
MONDO:0011295	schizophrenia 7
MONDO:0023267	goldstein hutt syndrome
MONDO:0023263	glyceraldehyde-3-phosphate dehydrogenase deficiency
MONDO:0011287	craniosynostosis-anal anomalies-porokeratosis syndrome
MONDO:0011286	autosomal recessive nonsyndromic deafness 13
MONDO:0011289	apraxia of eyelid opening
MONDO:0011288	spastic paraplegia, optic atrophy, microcephaly, and 10Y sex reversal
MONDO:0011281	congenital myasthenic syndrome 5
MONDO:0011280	schizophrenia 6
MONDO:0011283	mitochondrial DNA depletion syndrome 1
MONDO:0011282	tumor suppressor gene on chromosome 11
MONDO:0011285	age related macular degeneration 1
MONDO:0011284	astigmatism
MONDO:0023255	glossopalatine ankylosis micrognathia ear anomalies
MONDO:0023258	glycogen storage disease type 1 due to SLC37A4 mutation
MONDO:0023250	global disaccharide intolerance
MONDO:0011276	orofacial cleft 2
MONDO:0011275	acromesomelic dysplasia, Maroteaux type
MONDO:0011278	bile duct cysts
MONDO:0011277	leukoregulin
MONDO:0011279	autosomal recessive nonsyndromic deafness 17
MONDO:0011270	prostate cancer, hereditary, 8
MONDO:0011272	retinitis pigmentosa 25
MONDO:0011271	rigid spine muscular dystrophy 1
MONDO:0011274	Muenke syndrome
MONDO:0011273	H syndrome
MONDO:0023243	glass-chapman-hockley syndrome
MONDO:0023246	linear porokeratosis
MONDO:0023249	polyarticular juvenile rheumatoid arthritis
MONDO:0023240	gigantism advanced bone age hoarse cry
MONDO:0011265	tooth agenesis, selective, 2
MONDO:0011264	torsion dystonia 6
MONDO:0011267	intellectual disability, severe, with spasticity and pigmentary tapetoretinal degeneration
MONDO:0011266	myotonic dystrophy type 2
MONDO:0011269	psoriasis 2
MONDO:0011268	renal tubular acidosis, distal, 3, with or without sensorineural hearing loss
MONDO:0011261	spondyloepiphyseal dysplasia with coronal craniosynostosis, cataracts, cleft palate, and intellectual disability
MONDO:0011260	pancreatic lymphoma, familial
MONDO:0011263	skeletal dysplasia and progressive central nervous system degeneration, lethal
MONDO:0011262	camptodactyly, myopia, and fibrosis of the medial rectus muscle of eye
MONDO:0023290	grix Blankenship Peterson syndrome
MONDO:0023297	guttate psoriasis
MONDO:0023288	green sandford davison syndrome
MONDO:0023282	granulomatous hypophysitis
MONDO:0023283	ovarian granulosa cell tumor
MONDO:0023286	graphite pneumoconiosis
MONDO:0001763	ethmoid sinus cancer
MONDO:0001762	dentine erosion
MONDO:0001761	favism
MONDO:0001760	photokeratitis
MONDO:0001767	stenosis of lacrimal punctum
MONDO:0001766	eversion of lacrimal punctum
MONDO:0001765	polyneuropathy in collagen vascular disease
MONDO:0001764	ethmoidal sinus neoplasm
MONDO:0013749	ventricular septal defect 3
MONDO:0013747	atrioventricular septal defect 4
MONDO:0013748	ventricular septal defect 2
MONDO:0013752	hypoplastic left heart syndrome 2
MONDO:0013753	Charcot-Marie-Tooth disease axonal type 2P
MONDO:0013750	atrial septal defect 8
MONDO:0013751	cutis laxa, autosomal dominant 2
MONDO:0013756	hypertrophic osteoarthropathy, primary, autosomal recessive, 2
MONDO:0013757	congenital nongoitrous hypothryoidism 6
MONDO:0013754	cutis laxa, autosomal recessive, type 1B
MONDO:0013755	PYCR1-related de Barsy syndrome
MONDO:0001759	patent foramen ovale
MONDO:0001758	paranasal sinus sarcoma
MONDO:0001757	frontal sinus neoplasm
MONDO:0001774	posterior scleritis
MONDO:0001773	post-vaccinal encephalitis
MONDO:0001772	ulcer of anus and rectum
MONDO:0001771	infective urethral stricture
MONDO:0001778	dermoid cyst of skin
MONDO:0001777	acute gonococcal cystitis
MONDO:0001776	prostate calculus
MONDO:0001775	chronic duodenal ileus
MONDO:0013738	autosomal recessive nonsyndromic deafness 96
MONDO:0013739	chilblain lupus 2
MONDO:0013736	myopathy, centronuclear, 3
MONDO:0013737	hereditary spastic paraplegia 46
MONDO:0001770	gastrin secretion abnormality
MONDO:0013741	familial temporal lobe epilepsy 5
MONDO:0013742	familial mesial temporal lobe epilepsy with febrile seizures
MONDO:0013740	lethal occipital encephalocele-skeletal dysplasia syndrome
MONDO:0013745	Joubert syndrome 14
MONDO:0037735	sebaceous gland cancer
MONDO:0013746	ventricular septal defect 1
MONDO:0013743	autosomal systemic lupus erythematosus type 16
MONDO:0037736	infratentorial neoplasm
MONDO:0037737	peritoneal solitary fibrous tumor
MONDO:0013744	cataract 37
MONDO:0001769	acquired tear duct stenosis
MONDO:0001768	stenosis of lacrimal passage
MONDO:0001741	hyperparathyroidism
MONDO:0001740	cornea squamous cell carcinoma
MONDO:0025712	angioedema, hereditary, 4
MONDO:0001745	subserous uterine fibroid
MONDO:0001744	angle-closure glaucoma
MONDO:0001743	paranasal sinus lymphoma
MONDO:0001742	interval angle-closure glaucoma
MONDO:0025713	angioedema, hereditary, 7
MONDO:0013727	pregnancy loss, recurrent, susceptibility to, 1
MONDO:0037738	cauda equina cancer
MONDO:0013728	pregnancy loss, recurrent, susceptibility to, 2
MONDO:0037739	benign neoplasm of cauda equina
MONDO:0013725	colorectal cancer, hereditary nonpolyposis, type 7
MONDO:0013726	encephalopathy, lethal, due to defective mitochondrial peroxisomal fission 1
MONDO:0013729	pregnancy loss, recurrent, susceptibility to, 3
MONDO:0013730	graft versus host disease
MONDO:0013731	MEGF10-Related Myopathy
MONDO:0037742	endometrioid stromal and related neoplasms
MONDO:0037743	mediastinal soft tissue cancer
MONDO:0037744	neoplasm of retromolar area
MONDO:0013734	microphthalmia, syndromic 11
MONDO:0037745	fibromyxoid tumor
MONDO:0037746	malignant vaginal mixed epithelial and mesenchymal neoplasm
MONDO:0013735	microcephaly-cerebellar hypoplasia-cardiac conduction defect syndrome
MONDO:0037747	spinal injury
MONDO:0013732	glucocorticoid therapy, response to
MONDO:0037748	hyperlipoproteinemia
MONDO:0013733	accelerated tumor formation, susceptibility to
MONDO:0001738	osteopetrosis
MONDO:0001737	tetanus neonatorum
MONDO:0001736	neonatal infective mastitis
MONDO:0001735	paranasal sinus disease
MONDO:0025708	megacystis-microcolon-intestinal hypoperistalsis syndrome 2
MONDO:0037740	malignant central nervous system mesenchymal, non-meningothelial neoplasm
MONDO:0001739	purulent labyrinthitis
MONDO:0001752	alveolar periostitis
MONDO:0001751	cholestasis
MONDO:0001750	non-renal secondary hyperparathyroidism
MONDO:0001756	frontal sinus cancer
MONDO:0025701	leukodystrophy, hypomyelinating, 22
MONDO:0001755	vaginal carcinosarcoma
MONDO:0001754	eclampsia
MONDO:0001753	female infertility of uterine origin
MONDO:0013716	aortic aneurysm, familial abdominal, 4
MONDO:0013717	asphyxiating thoracic dystrophy 5
MONDO:0013714	mannose-binding lectin deficiency
MONDO:0013715	amyotrophic lateral sclerosis type 16
MONDO:0013718	nephronophthisis 13
MONDO:0013719	cranioectodermal dysplasia 4
MONDO:0013720	complement component 4b deficiency
MONDO:0013723	bacteremia, susceptibility to, 1
MONDO:0013724	bacteremia, susceptibility to, 2
MONDO:0013721	complement component 4a deficiency
MONDO:0013722	hypomyelinating leukodystrophy 8 with or without oligodontia and-or hypogonadotropic hypogonadism
MONDO:0001749	cortical senile cataract
MONDO:0001748	maxillary sinus carcinoma
MONDO:0001747	tibial collateral ligament bursitis
MONDO:0001746	optic disk drusen
MONDO:0023111	familial capillaro-venous leptomeningeal angiomatosis
MONDO:0023113	familial colorectal cancer
MONDO:0011129	glaucoma type 1C
MONDO:0011133	deaf blind hypopigmentation syndrome, Yemenite type
MONDO:0013796	chromosome 17q12 duplication syndrome
MONDO:0011132	T-cell immunodeficiency, congenital alopecia, and nail dystrophy
MONDO:0013797	chromosome 17q12 deletion syndrome
MONDO:0013794	thrombocythemia 3
MONDO:0011135	superior transverse scapular ligament, calcification of, familial
MONDO:0011134	curry-Jones syndrome
MONDO:0013795	fibrochondrogenesis 2
MONDO:0011137	retinitis pigmentosa 19
MONDO:0011136	Quebec platelet disorder
MONDO:0011139	preaxial hallucal polydactyly
MONDO:0013798	chromosome 16q22 deletion syndrome
MONDO:0011138	systemic lupus erythematosus, susceptibility to, 1
MONDO:0013799	efavirenz, poor metabolism of
MONDO:0013792	intracerebral hemorrhage
MONDO:0013793	encephalomyopathy, mitochondrial, due to voltage-dependent anion channel deficiency
MONDO:0013790	mirror movements 2
MONDO:0011131	tricho-oculo-dermo-vertebral syndrome
MONDO:0011130	sebaceous gland hyperplasia, familial presenile
MONDO:0013791	thrombophilia due to protein S deficiency, autosomal recessive
MONDO:0023100	facial clefting corpus callosum agenesis
MONDO:0023101	facio digito genital syndrome recessive form
MONDO:0023102	facio skeletal genital syndrome rippberger type
MONDO:0023106	Fairbank disease
MONDO:0011119	iridogoniodysgenesis
MONDO:0011118	bilineal acute myeloid leukemia
MONDO:0013785	intellectual disability, autosomal recessive 34
MONDO:0011122	obesity disorder
MONDO:0013786	cone-rod dystrophy 16
MONDO:0011121	paragangliomas 2
MONDO:0011124	spondyloepimetaphyseal dysplasia-abnormal dentition syndrome
MONDO:0013783	microphthalmia, isolated, with coloboma 7
MONDO:0011123	type 1 diabetes mellitus 15
MONDO:0013784	lethal neonatal spasticity-epileptic encephalopathy syndrome
MONDO:0011126	acute insulin response
MONDO:0013789	DDOST-CDG
MONDO:0011125	trichothiodystrophy 1, photosensitive
MONDO:0013787	psychomotor retardation, epilepsy, and craniofacial dysmorphism
MONDO:0011128	Sheldon-hall syndrome
MONDO:0013788	Usher syndrome type 3B
MONDO:0011127	Bartter disease type 1
MONDO:0013781	pseudohypoaldosteronism type 2D
MONDO:0013782	pseudohypoaldosteronism type 2E
MONDO:0011120	neural tube defects, folate-sensitive
MONDO:0013780	retinitis pigmentosa 63
MONDO:0001785	malignant secondary hypertension
MONDO:0001784	malignant renovascular hypertension
MONDO:0001783	endometrial stromal nodule
MONDO:0001782	mature cataract
MONDO:0001789	neurofibroma of spinal cord
MONDO:0001788	nutmeg liver
MONDO:0001787	hepatic infarction
MONDO:0001786	uterine inflammatory disease
MONDO:0011108	Stüve-Wiedemann syndrome
MONDO:0011107	congenital hypotrichosis with juvenile macular dystrophy
MONDO:0013769	atrioventricular septal defect 5
MONDO:0011109	multiple epiphyseal dysplasia, Lowry type
MONDO:0001781	uterine corpus adenomatoid tumor
MONDO:0001780	premature ejaculation
MONDO:0013774	trigonocephaly 2
MONDO:0011111	horns in sheep
MONDO:0011110	dyssegmental dysplasia-glaucoma syndrome
MONDO:0013775	thrombomodulin-related bleeding disorder
MONDO:0011113	Charcot-Marie-Tooth disease type 4C
MONDO:0013772	congenital cataract-hearing loss-severe developmental delay syndrome
MONDO:0013773	porencephaly 2
MONDO:0011112	Wilms tumor 5
MONDO:0013778	pseudohypoaldosteronism type 2C
MONDO:0011115	spastic paraplegia and Evans syndrome
MONDO:0011114	familial multiple trichoepithelioma
MONDO:0013779	Wiskott-Aldrich syndrome 2
MONDO:0013776	spastic ataxia 5
MONDO:0011117	iris pigment epithelium anomalies
MONDO:0011116	lung agenesis-heart defect-thumb anomalies syndrome
MONDO:0013777	pseudohypoaldosteronism type 2B
MONDO:0001779	vaginal squamous papilloma
MONDO:0013770	atrial septal defect 9
MONDO:0013771	transient infantile hypertriglyceridemia and hepatosteatosis
MONDO:0001796	epidermodysplasia verruciformis
MONDO:0001795	plantar wart
MONDO:0001794	Pthirus pubis infestation
MONDO:0001793	excessive tearing
MONDO:0001799	localized anterior staphyloma
MONDO:0001798	hypermobility syndrome
MONDO:0001797	chancroid
MONDO:0013758	Charcot-Marie-Tooth disease dominant intermediate E
MONDO:0013759	melanoma, cutaneous malignant, susceptibility to, 8
MONDO:0001792	epiphora due to insufficient drainage
MONDO:0001791	neonatal urinary tract infectious disease
MONDO:0001790	spinal cord lipoma
MONDO:0011100	microcephaly, retinitis pigmentosa, and sutural cataract
MONDO:0013763	Joubert syndrome 15
MONDO:0013764	Joubert syndrome 16
MONDO:0011102	autosomal dominant nonsyndromic deafness 12
MONDO:0013761	childhood encephalopathy due to thiamine pyrophosphokinase deficiency
MONDO:0013762	lipoic acid synthetase deficiency
MONDO:0011101	peroxisome biogenesis disorder 1B
MONDO:0011104	cataract 3 multiple types
MONDO:0013767	autoimmune lymphoproliferative syndrome type 4
MONDO:0011103	autosomal dominant nonsyndromic deafness 3A
MONDO:0013768	arterial calcification, generalized, of infancy, 2
MONDO:0011106	facial dysmorphism-lens dislocation-anterior segment abnormalities-spontaneous filtering blebs syndrome
MONDO:0013765	coronary heart disease, susceptibility to, 6
MONDO:0011105	alacrima, congenital, autosomal recessive
MONDO:0013766	familial cold autoinflammatory syndrome 3
MONDO:0013760	congenital ichthyosis-intellectual disability-spastic quadriplegia syndrome
MONDO:0001723	progressive peripheral pterygium
MONDO:0001722	central pterygium
MONDO:0001721	urethral intrinsic sphincter deficiency
MONDO:0001720	gonococcal synovitis
MONDO:0013705	intellectual disability, autosomal recessive 19
MONDO:0013706	intellectual disability, autosomal recessive 23
MONDO:0013703	intellectual disability, autosomal recessive 33
MONDO:0013704	intellectual disability, autosomal recessive 30
MONDO:0013709	intellectual disability, autosomal recessive 28
MONDO:0013707	intellectual disability, autosomal recessive 24
MONDO:0013708	intellectual disability, autosomal recessive 25
MONDO:0013712	surfactant metabolism dysfunction, pulmonary, 5
MONDO:0013713	dengue virus, susceptibility to
MONDO:0013710	colorectal cancer, hereditary nonpolyposis, type 5
MONDO:0013711	peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome
MONDO:0001716	corneal argyrosis
MONDO:0001715	basilar artery occlusion
MONDO:0001714	bejel
MONDO:0001713	inherited aplastic anemia
MONDO:0001719	gonococcal bursitis
MONDO:0001718	scleritis
MONDO:0001717	posterior corneal pigmentation
MONDO:0001730	urethral syndrome
MONDO:0001734	tuberous sclerosis
MONDO:0001733	occlusion of tributary of retinal vein
MONDO:0001732	trigonitis
MONDO:0001731	benign vaginal mixed epithelial and mesenchymal neoplasm
MONDO:0013701	MRT32
MONDO:0013702	intellectual disability, autosomal recessive 27
MONDO:0013700	pancreatic triacylglycerol lipase deficiency
MONDO:0001727	active cochleovestibular Meniere disease
MONDO:0001726	childhood disintegrative disease
MONDO:0001725	balanitis xerotica obliterans
MONDO:0001724	supraglottis cancer
MONDO:0001729	active cochlear Meniere disease
MONDO:0001728	active vestibular Meniere disease
MONDO:0001701	gastrointestinal anthrax
MONDO:0001700	megaloblastic anemia
MONDO:0001712	alexia
MONDO:0001711	hepatic encephalopathy
MONDO:0001710	perforation of bile duct
MONDO:0001705	pure red-cell aplasia
MONDO:0001704	vaginal glandular neoplasm
MONDO:0001703	color vision disorder
MONDO:0001702	labia majora carcinoma
MONDO:0001709	hypercalcemic sarcoidosis
MONDO:0001708	pulmonary sarcoidosis
MONDO:0001707	cardiac sarcoidosis
MONDO:0001706	cerebral sarcoidosis
MONDO:0023155	fibula aplasia complex brachydactyly
MONDO:0023156	fibular aplasia
MONDO:0023157	fibular hypoplasia scapulo pelvic dysplasia absent
MONDO:0023158	Fitz-Hugh-Curtis syndrome
MONDO:0023152	fibrocartilaginous embolism
MONDO:0023153	tuberculous ascites
MONDO:0023154	fibromatosis multiple non ossifying
MONDO:0011177	ectodermal dysplasia 4, hair/nail type
MONDO:0011176	intestinal hypomagnesemia 1
MONDO:0011179	leishmaniasis, tegumentary, susceptibility to
MONDO:0011178	infantile convulsions and choreoathetosis
MONDO:0011171	odonto-tricho-ungual-digito-palmar syndrome
MONDO:0011170	autosomal recessive limb-girdle muscular dystrophy type 2G
MONDO:0011173	thrombocythemia 2
MONDO:0011172	otofacioosseous-gonadal syndrome
MONDO:0011175	Friedreich ataxia 2
MONDO:0011174	hyperzincemia with functional zinc depletion
MONDO:0023147	fetal parainfluenza virus type 3 syndrome
MONDO:0023148	fetal phenothiazine syndrome
MONDO:0023149	infection due to clostridium perfringens
MONDO:0023140	fenton Wilkinson Toselano syndrome
MONDO:0023141	antihypertensive drugs antenatal exposure syndrome
MONDO:0023142	fetal brain disruption sequence
MONDO:0023143	fetal enterovirus syndrome
MONDO:0011166	lymphedema-atrial septal defects-facial changes syndrome
MONDO:0011165	glomerulopathy with fibronectin deposits 2
MONDO:0011168	type 1 diabetes mellitus 10
MONDO:0011167	type 1 diabetes mellitus 6
MONDO:0011169	keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome
MONDO:0011160	autosomal recessive nonsyndromic deafness 15
MONDO:0011162	cataract 14 multiple types
MONDO:0011161	sperm-specific antigen 1
MONDO:0011164	malignant hyperthermia, susceptibility to, 6
MONDO:0011163	malignant hyperthermia, susceptibility to, 5
MONDO:0023133	Faye-Petersen-Ward-Carey syndrome
MONDO:0023134	febrile ulceronecrotic mucha-habermann disease
MONDO:0023137	feigenbaum Bergeron syndrome
MONDO:0023138	Feingold trainer syndrome
MONDO:0011155	vacuolar Neuromyopathy
MONDO:0011154	acrofacial dysostosis, Palagonia type
MONDO:0011157	Gomez-Lopez-Hernandez syndrome
MONDO:0011156	progressive familial intrahepatic cholestasis type 2
MONDO:0011159	autosomal dominant nonsyndromic deafness 13
MONDO:0011158	autoimmune lymphoproliferative syndrome type 1
MONDO:0011151	exudative vitreoretinopathy 4
MONDO:0011150	acroosteolysis-keloid-like lesions-premature aging syndrome
MONDO:0011153	hyperinsulinemic hypoglycemia, familial, 2
MONDO:0011152	PHGDH deficiency
MONDO:0023122	familial prostate carcinoma
MONDO:0023124	familial pulmonary arterial hypertension leucopenia and atrial septal defect
MONDO:0023129	Fara Chlupackova syndrome
MONDO:0023121	familial partial paralysis
MONDO:0011144	neuronal ceroid lipofuscinosis 6
MONDO:0011143	cone-rod dystrophy 6
MONDO:0011146	tetrasomy 12p
MONDO:0011145	colobomatous microphthalmia - obesity - hypogenitalism - intellectual disability syndrome
MONDO:0011148	Spondylospinal thoracic dysostosis
MONDO:0011147	chromosome 18q deletion syndrome
MONDO:0011149	premature aging syndrome, Okamoto type
MONDO:0023119	familial myelofibrosis
MONDO:0011140	benign familial neonatal-infantile seizures
MONDO:0011142	Ehlers-Danlos syndrome, musculocontractural type
MONDO:0011141	folate level in erythrocytes
MONDO:0023199	frontonasal dysplasia phocomelic upper limbs
MONDO:0023191	Freire-Maia odontotrichomelic syndrome
MONDO:0023193	Friedman Goodman syndrome
MONDO:0023194	frints de Smet Fabry Fryns syndrome
MONDO:0023196	frontonasal malformation cloacal exstrophy
MONDO:0023197	frontonasal dysplasia Klippel feil syndrome
MONDO:0023188	Freiberg disease
MONDO:0023180	fragile X syndrome type 3
MONDO:0023182	Franceschini Vardeu Guala syndrome
MONDO:0023186	Fraser Jequier Chen syndrome
MONDO:0035117	PUM1-associated developmental disability-ataxia-seizure syndrome
MONDO:0035112	acute myeloid leukemia with BCR-ABL1
MONDO:0023178	fragile X syndrome type 1
MONDO:0023179	fragile X syndrome type 2
MONDO:0023170	focal or multifocal malformations in neuronal migration
MONDO:0023171	foix chavany Marie syndrome
MONDO:0023174	follicular lymphoreticuloma
MONDO:0023175	Fontaine farriaux blanckaert syndrome
MONDO:0023176	formaldehyde poisoning
MONDO:0035122	GRIN2B-related developmental delay, intellectual disability and autism spectrum disorder
MONDO:0011199	nephropathy, progressive tubulointerstitial, with cholestatic liver disease
MONDO:0035121	myeloid/lymphoid neoplasm associated with JAK2 rearrangement
MONDO:0011198	spondyloepimetaphyseal dysplasia, Missouri type
MONDO:0011191	capillary infantile hemangioma
MONDO:0011190	nephronophthisis 2
MONDO:0011193	cone dystrophy 3
MONDO:0011192	autosomal recessive nonsyndromic deafness 18A
MONDO:0011195	Usher syndrome type 1E
MONDO:0011194	Alzheimer disease 5
MONDO:0011197	hereditary thermosensitive neuropathy
MONDO:0035124	linear hypopigmentation and craniofacial asymmetry with acral, ocular and brain anomalies
MONDO:0011196	amyotrophic lateral sclerosis type 5
MONDO:0023167	focal alopecia congenital megalencephaly
MONDO:0023161	viral myocarditis
MONDO:0023164	viral pericarditis
MONDO:0023165	florid cystic endosalpingiosis of the uterus
MONDO:0011188	arrhythmogenic right ventricular dysplasia 3
MONDO:0035133	PHIP-related behavioral problems-intellectual disability-obesity-dysmorphic features syndrome
MONDO:0011187	polydactyly, postaxial, type A2
MONDO:0011189	arrhythmogenic right ventricular dysplasia 4
MONDO:0011180	broad terminal phalanges, familial
MONDO:0011182	trimethylaminuria
MONDO:0011181	fibrosis of extraocular muscles, congenital, 2
MONDO:0011184	childhood apraxia of speech
MONDO:0037792	carbohydrate metabolism disease
MONDO:0011183	Paget disease of bone 2, early-onset
MONDO:0035136	isolated melanotic schwannoma
MONDO:0011186	Usher syndrome type 1F
MONDO:0011185	Thiel-Behnke corneal dystrophy
MONDO:0056797	neurodevelopmental disorder with midbrain and hindbrain malformations
MONDO:0056798	disorder of appendix
MONDO:0056799	synovium disease
MONDO:0056795	X-linked spermatogenic failure 1
MONDO:0056796	obstructive nephropathy
MONDO:0017150	pulmonary arterial hypertension associated with another disease
MONDO:0017151	pulmonary arterial hypertension associated with connective tissue disease
MONDO:0032788	cerebellar atrophy with seizures and variable developmental delay
MONDO:0032789	intellectual developmental disorder, autosomal recessive 71
MONDO:0005167	fibroma
MONDO:0029134	severe combined immunodeficiency due to CARMIL2 deficiency
MONDO:0005166	osteoma
MONDO:0029133	muscular dystrophy, limb-girdle, autosomal dominant 4
MONDO:0029132	Liddle syndrome 3
MONDO:0005169	neoplasm of mature T-cells or NK-cells
MONDO:0044777	premature ovarian failure 14
MONDO:0044776	premature ovarian failure 10
MONDO:0029131	peripheral neuropathy, autosomal recessive, with or without impaired intellectual development
MONDO:0005168	neoplasm of immature B and T cells
MONDO:0005163	simian immunodeficiency virus infection
MONDO:0029138	developmental and epileptic encephalopathy, 67
MONDO:0029137	deafness, autosomal dominant 74
MONDO:0005162	influenza infection
MONDO:0005165	benign neoplasm
MONDO:0029136	muscular dystrophy, limb-girdle, autosomal recessive 23
MONDO:0029135	muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 8
MONDO:0005164	fibrosarcoma
MONDO:0032790	neurodevelopmental disorder with coarse facies and mild distal skeletal abnormalities
MONDO:0005161	human papilloma virus infection
MONDO:0005160	aortic aneurysm
MONDO:0044768	vagus nerve paraganglioma
MONDO:0029130	polydactyly, postaxial, type A8
MONDO:0044767	childhood adrenal gland pheochromocytoma
MONDO:0020799	basal cell neoplasm
MONDO:0020798	hypoparathyroidism, familial isolated, 2
MONDO:0030134	oculopharyngodistal myopathy 2
MONDO:0017156	pulmonary arterial hypertension associated with chronic hemolytic anemia
MONDO:0032797	myopathy, congenital, with tremor
MONDO:0032798	ichthyotic keratoderma, spasticity, hypomyelination, and dysmorphic facial features
MONDO:0017157	pulmonary hypertension owing to lung disease and/or hypoxia
MONDO:0017158	pulmonary hypertension with unclear multifactorial mechanism
MONDO:0032795	intellectual developmental disorder 59
MONDO:0017159	syndrome with pulmonary hypertension as a major feature
MONDO:0032796	hyper-ige recurrent infection syndrome 4, autosomal recessive
MONDO:0017152	pulmonary arterial hypertension associated with congenital heart disease
MONDO:0032793	O'Donnell-Luria-Rodan syndrome
MONDO:0017153	pulmonary arterial hypertension associated with HIV infection
MONDO:0032794	leber congenital amaurosis 19
MONDO:0017154	pulmonary arterial hypertension associated with portal hypertension
MONDO:0032791	Coffin-Siris syndrome 10
MONDO:0032792	neuropathy, hereditary motor and sensory, type VIc, with optic atrophy
MONDO:0017155	pulmonary arterial hypertension associated with schistosomiasis
MONDO:0017140	L1 syndrome
MONDO:0032799	mitochondrial DNA depletion syndrome 16 (hepatic type)
MONDO:0020797	decompression sickness
MONDO:0044786	solid pseudopapillary neoplasm of the pancreas
MONDO:0005178	osteoarthritis
MONDO:0020796	Silver-Russell syndrome 1
MONDO:0044785	desmoplastic melanoma
MONDO:0005177	serous cystadenoma
MONDO:0020795	Silver-Russell syndrome 5
MONDO:0044788	perihilar intrahepatic cholangiocarcinoma
MONDO:0044787	nasal cavity and paranasal sinus squamous cell carcinoma
MONDO:0020794	colorectal medullary carcinoma
MONDO:0005179	ovarian adenoma benign
MONDO:0005174	acute hypotension
MONDO:0044782	esophageal ulcer
MONDO:0020793	oculopharyngodistal myopathy 1
MONDO:0044781	nephrotic syndrome of childhood - steroid sensitive
MONDO:0005173	actinic keratosis
MONDO:0020792	dwarfism with tall vertebrae
MONDO:0005176	benign insulitis
MONDO:0044784	myxoma
MONDO:0020791	corneal dystrophy, Meesmann, 1
MONDO:0005175	aggressive insulitis
MONDO:0020790	gaze palsy, familial horizontal, with progressive scoliosis 1
MONDO:0044783	solid papillary breast carcinoma
MONDO:0005170	myeloid neoplasm
MONDO:0005172	skeletal system disease
MONDO:0005171	chronic myeloproliferative disorder
MONDO:0017149	drug- or toxin-induced pulmonary arterial hypertension
MONDO:0044778	nodular lymphocyte predominant Hodgkin lymphoma
MONDO:0020789	pseudo-TORCH syndrome 1
MONDO:0020788	hypomagnesemia, seizures, and intellectual disability 2
MONDO:0020787	hypomagnesemia, seizures, and intellectual disability 1
MONDO:0017145	beta-thalassemia and related diseases
MONDO:0017146	sickle cell disease and related diseases
MONDO:0017147	idiopathic pulmonary arterial hypertension
MONDO:0017148	heritable pulmonary arterial hypertension
MONDO:0017141	hemorrhagic disorder due to a constitutional thrombocytopenia
MONDO:0017142	hemorrhagic disorder due to a qualitative platelet defect
MONDO:0017143	genetic infertility
MONDO:0017144	alpha-thalassemia and related diseases
MONDO:0019791	recessive mitochondrial ataxia syndrome
MONDO:0044791	combined hepatocellular carcinoma and cholangiocarcinoma
MONDO:0019790	neuroleptic malignant syndrome
MONDO:0044790	congenital melanocytic nevus
MONDO:0005149	pulmonary hypertension
MONDO:0005148	type 2 diabetes mellitus
MONDO:0044797	desmoplastic nevus
MONDO:0005145	sporadic amyotrophic lateral sclerosis
MONDO:0020786	short sleep, familial natural, 2
MONDO:0044796	spindle cell nevus
MONDO:0020785	capillary malformation-arteriovenous malformation 2
MONDO:0005144	familial amyotrophic lateral sclerosis
MONDO:0005147	type 1 diabetes mellitus
MONDO:0020784	short sleep, familial natural, 1
MONDO:0005146	post-traumatic stress disorder
MONDO:0020783	capillary malformation-arteriovenous malformation 1
MONDO:0044793	spitz nevus
MONDO:0020782	chronic gingivitis
MONDO:0005141	Pseudomonas infection
MONDO:0005140	ovarian carcinoma
MONDO:0044792	large congenital melanocytic nevus
MONDO:0020781	encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 1
MONDO:0020780	cone-rod dystrophy and hearing loss 2
MONDO:0044795	epithelioid cell nevus
MONDO:0005143	Pseudomonas aeruginosa PA14 infection
MONDO:0005142	Pseudomonas aeruginosa CF5 infection
MONDO:0044794	benign melanocytic skin nevus
MONDO:0020779	cartilage development disorder
MONDO:0017138	Opitz G/BBB syndrome
MONDO:0017139	oromandibular-limb hypogenesis syndrome
MONDO:0020778	cone-rod dystrophy and hearing loss 1
MONDO:0044789	digital papillary eccrine carcinoma
MONDO:0020777	congenital disorder of glycosylation with defective fucosylation 2
MONDO:0020776	chlamydiaceae infections
MONDO:0019797	acrodysostosis
MONDO:0017134	odonto-onycho dysplasia-alopecia syndrome
MONDO:0019796	acrocephalosyndactyly
MONDO:0017135	olivopontocerebellar atrophy-deafness syndrome
MONDO:0019799	hepatoerythropoietic porphyria
MONDO:0017136	omodysplasia
MONDO:0017137	onchocerciasis
MONDO:0019798	acute hepatic porphyria
MONDO:0019793	autosomal dominant cerebellar ataxia type III
MONDO:0017130	genetic urogenital tumor
MONDO:0017131	genetic cardiac anomaly
MONDO:0019792	autosomal dominant cerebellar ataxia type I
MONDO:0019795	acalvaria
MONDO:0017132	hereditary ATTR amyloidosis
MONDO:0019794	autosomal dominant cerebellar ataxia type IV
MONDO:0017133	genetic systemic or rheumatologic disease
MONDO:0019780	anotia
MONDO:0005159	prostate carcinoma
MONDO:0005156	encephalomyelitis
MONDO:0020775	congenital disorder of glycosylation with defective fucosylation 1
MONDO:0005155	cirrhosis of liver
MONDO:0020774	Menke-Hennekam syndrome
MONDO:0020773	cerebrospinal fluid rhinorrhea
MONDO:0005158	coronary heart disease
MONDO:0005157	lymphoid neoplasm
MONDO:0020772	epilepsy, juvenile absence, susceptibility to, 1
MONDO:0005152	hypopituitarism
MONDO:0020771	spinocerebellar ataxia, autosomal recessive, with axonal neuropathy
MONDO:0005151	endocrine system disease
MONDO:0020770	spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 3
MONDO:0005154	liver disease
MONDO:0005153	cervical adenocarcinoma
MONDO:0005150	age-related macular degeneration
MONDO:0020769	Menke-Hennekam syndrome 2
MONDO:0017127	inherited soft tissue tumor
MONDO:0020768	X-linked deafness
MONDO:0020767	cauda equina syndrome with neurogenic bladder
MONDO:0019789	cytophagic histiocytic panniculitis
MONDO:0017128	inherited digestive tract tumor
MONDO:0017129	inherited cardiac tumor
MONDO:0020766	neuropathy, congenital hypomyelinating, 3
MONDO:0020765	neuropathy, congenital hypomyelinating, 2
MONDO:0017123	arthrogryposis-renal dysfunction-cholestasis syndrome
MONDO:0019786	severe intellectual disability-epilepsy-anal anomalies-distal phalangeal hypoplasia
MONDO:0019785	15q24 microdeletion syndrome
MONDO:0017124	noma
MONDO:0017125	oculofaciocardiodental syndrome
MONDO:0019788	non-secreting paraganglioma
MONDO:0019787	autoimmune enteropathy
MONDO:0017126	oculo-skeletal-renal syndrome
MONDO:0019782	humero-ulnar synostosis
MONDO:0017120	other syndrome with a central nervous system malformation as major feature
MONDO:0019781	astrocytoma (excluding glioblastoma)
MONDO:0019784	12q14 microdeletion syndrome
MONDO:0017121	syndrome with a Dandy-Walker malformation as major feature
MONDO:0019783	neovascular glaucoma
MONDO:0017122	genetic syndrome with corpus callosum agenesis/dysgenesis as a major feature
MONDO:0017192	sporadic secreting paraganglioma
MONDO:0017193	symptomatic form of Coffin-Lowry syndrome in female carriers
MONDO:0017194	Blount disease
MONDO:0032748	spermatogenic failure 38
MONDO:0017195	Bruck syndrome
MONDO:0032749	deafness, autosomal recessive 94
MONDO:0032746	hydatidiform mole, recurrent, 3
MONDO:0032747	hydatidiform mole, recurrent, 4
MONDO:0032744	spermatogenic failure 37
MONDO:0017190	sporadic pheochromocytoma/secreting paraganglioma
MONDO:0032745	developmental delay with variable intellectual impairment and behavioral abnormalities
MONDO:0017191	sporadic pheochromocytoma
MONDO:0044727	pancreatic carcinoma with mixed differentiation
MONDO:0044724	3-methylglutaconic aciduria type 9
MONDO:0044723	3-methylglutaconic aciduria type 8
MONDO:0044726	psychomotor regression-oculomotor apraxia-movement disorder-nephropathy syndrome
MONDO:0044725	combined immunodeficiency due to GINS1 deficiency
MONDO:0032753	spastic ataxia 9, autosomal recessive
MONDO:0032751	arthrogryposis, distal, type 2B3
MONDO:0032752	developmental and epileptic encephalopathy, 75
MONDO:0017196	osteogenesis imperfecta-retinopathy-seizures-intellectual disability syndrome
MONDO:0032750	arthrogryposis, distal, type 2B2
MONDO:0017197	osteopathia striata-pigmentary dermopathy-white forelock syndrome
MONDO:0017198	osteopetrosis
MONDO:0017199	osteoporosis-macrocephaly-blindness-joint hyperlaxity syndrome
MONDO:0017181	hypnic headache
MONDO:0017182	familial hyperinsulinism
MONDO:0032759	intellectual developmental disorder with short stature and variable skeletal anomalies
MONDO:0017183	hyperinsulinism due to UCP2 deficiency
MONDO:0017184	autosomal dominant hyperinsulinism due to SUR1 deficiency
MONDO:0032757	ciliary dyskinesia, primary, 41
MONDO:0032758	neurodegeneration, early-onset, with choreoathetoid movements and microcytic anemia
MONDO:0032755	neurodevelopmental disorder with or without variable brain abnormalities; NEDBA
MONDO:0032756	long qt syndrome 8
MONDO:0017180	10q22.3q23.3 microduplication syndrome
MONDO:0044742	autosomal recessive epidermolytic ichthyosis
MONDO:0044744	prekallikrein deficiency
MONDO:0044743	major salivary gland cancer
MONDO:0044740	salivary gland squamous cell carcinoma
MONDO:0044739	Stevens-Johnson syndrome/toxic epidermal necrolysis overlap syndrome
MONDO:0044738	Gabriele de Vries syndrome
MONDO:0044737	autosomal recessive complex spastic paraplegia due to kennedy pathway dysfunction
MONDO:0017189	adult-onset non-insulinoma persistent hyperinsulinemic hypoglycemia
MONDO:0032764	Khan-Khan-Katsanis syndrome
MONDO:0032765	bleeding disorder, platelet-type, 22
MONDO:0032762	deafness, autosomal recessive 115
MONDO:0032763	immunodeficiency 62
MONDO:0017185	autosomal dominant hyperinsulinism due to Kir6.2 deficiency
MONDO:0032760	developmental delay with or without dysmorphic facies and autism
MONDO:0017186	diazoxide-resistant hyperinsulinism
MONDO:0032761	deafness, autosomal recessive 114
MONDO:0017187	diazoxide-resistant focal hyperinsulinism due to SUR1 deficiency
MONDO:0017188	diazoxide-resistant focal hyperinsulinism due to Kir6.2 deficiency
MONDO:0017170	idiopathic recurrent stupor
MONDO:0017171	mucopolysaccharidosis type 6, rapidly progressing
MONDO:0017172	mucopolysaccharidosis type 6, slowly progressing
MONDO:0017173	non-syndromic male infertility due to sperm motility disorder
MONDO:0030105	galactosemia 4
MONDO:0032768	developmental and epileptic encephalopathy, 76
MONDO:0032766	hypoalphalipoproteinemia, primary, 2
MONDO:0032767	paragangliomas 6
MONDO:0044753	lumbar spinal stenosis
MONDO:0005189	internal carotid artery stenosis
MONDO:0005188	iatrogenic Kaposi's sarcoma
MONDO:0005185	chronic childhood arthritis
MONDO:0005184	pancreatic ductal adenocarcinoma
MONDO:0005187	human herpesvirus 8 infection
MONDO:0044751	chronic diarrheal disease
MONDO:0005186	cocaine dependence
MONDO:0044750	lassa virus infectious disease
MONDO:0005181	progressive external ophthalmoplegia
MONDO:0005180	Parkinson disease
MONDO:0044749	X-linked congenital stationary night blindness
MONDO:0005183	ovarian cystadenoma
MONDO:0005182	serous cystadenofibroma
MONDO:0044746	zoonotic bacterial infection
MONDO:0044745	nervous system injury
MONDO:0044748	anaplasmosis in cattle
MONDO:0044747	human anaplasmosis
MONDO:0017178	osteochondritis dissecans
MONDO:0032775	neurodevelopmental disorder with seizures and speech and walking impairment
MONDO:0032776	deafness, autosomal recessive 99
MONDO:0017179	limbic encephalitis with caspr2 antibodies
MONDO:0032773	uridine-cytidineuria
MONDO:0032774	cerebellar, ocular, craniofacial, and genital syndrome
MONDO:0017174	Machado-Joseph disease type 1
MONDO:0032771	paragangliomas 7
MONDO:0017175	Machado-Joseph disease type 2
MONDO:0032772	brain abnormalities, neurodegeneration, and dysosteosclerosis
MONDO:0017176	Machado-Joseph disease type 3
MONDO:0017177	hemihyperplasia-multiple lipomatosis syndrome
MONDO:0032770	intellectual developmental disorder with severe speech and ambulation defects
MONDO:0017160	behavioral variant of frontotemporal dementia
MONDO:0017161	frontotemporal dementia with motor neuron disease
MONDO:0017162	imperforate oropharynx-costo vetebral anomalies syndrome
MONDO:0030116	silver-russell syndrome 2
MONDO:0032779	neurodevelopmental disorder with microcephaly and structural brain anomalies
MONDO:0030118	silver-russell syndrome 4
MONDO:0032777	generalized epilepsy with febrile seizures plus, type 10
MONDO:0032778	arthrogryposis multiplex congenita 3, myogenic type
MONDO:0044764	benign choroid plexus neoplasm
MONDO:0029145	orofacial cleft 8
MONDO:0029144	extraoral halitosis due to methanethiol oxidase deficiency
MONDO:0044763	diarrheal disease secondary to decreased bowel motility
MONDO:0005199	peripartum cardiomyopathy
MONDO:0044766	Marfan Syndrome 3
MONDO:0029143	intellectual developmental disorder with hypertelorism and distinctive facies
MONDO:0044765	steroid-resistant nephrotic syndrome
MONDO:0029142	deafness, autosomal recessive 111
MONDO:0005196	teratozoospermia
MONDO:0005195	septic peritonitis
MONDO:0029148	spermatogenic failure 34
MONDO:0005198	vulvar intraepithelial neoplasia
MONDO:0044762	diarrheal disease secondary to increased bowel motility
MONDO:0029147	spermatogenic failure 33
MONDO:0005197	thymus neoplasm
MONDO:0029146	Saul-Wilson syndrome
MONDO:0005192	exocrine pancreatic carcinoma
MONDO:0005191	metastatic melanoma
MONDO:0005194	Rotavirus infection
MONDO:0005193	prostate intraepithelial neoplasia
MONDO:0029141	Usher syndrome, type 4
MONDO:0029140	glycosylphosphatidylinositol biosynthesis defect 18
MONDO:0005190	macroglobulinemia
MONDO:0017167	malignant epithelial tumor of salivary glands
MONDO:0032786	Noonan syndrome 11
MONDO:0032787	holoprosencephaly 12 with or without pancreatic agenesis
MONDO:0017168	benign epithelial tumor of salivary glands
MONDO:0017169	multiple endocrine neoplasia
MONDO:0032784	neurodevelopmental disorder with seizures and nonepileptic hyperkinetic movements
MONDO:0032785	polydactyly, postaxial, type a10
MONDO:0017163	hemolytic disease due to fetomaternal alloimmunization
MONDO:0032782	immunodeficiency 63 with lymphoproliferation and autoimmunity
MONDO:0032783	aortic valve disease 3
MONDO:0017164	hemolytic disease of the newborn with Kell alloimmunization
MONDO:0017165	bile acid CoA ligase deficiency and defective amidation
MONDO:0032780	hypotonia, hypoventilation, impaired intellectual development, dysautonomia, epilepsy, and eye abnormalities
MONDO:0032781	congenital hypotonia, epilepsy, developmental delay, and digital anomalies
MONDO:0017166	rare tumor of salivary glands
MONDO:0005208	amelanotic skin melanoma
MONDO:0032827	epilepsy, idiopathic generalized, susceptibility to, 16
MONDO:0005207	choriocarcinoma
MONDO:0032828	spastic tetraplegia and axial hypotonia, progressive
MONDO:0007869	Kyrle disease
MONDO:0005209	cutaneous T-cell lymphoma
MONDO:0032826	nephrotic syndrome, type 21
MONDO:0007867	nonsyndromic congenital nail disorder 2
MONDO:0032823	intellectual developmental disorder 60 with seizures
MONDO:0005204	primary antiphospholipid syndrome
MONDO:0005203	ischemia reperfusion injury
MONDO:0007868	hyperekplexia 1
MONDO:0032824	glycosylphosphatidylinositol biosynthesis defect 21
MONDO:0005206	renal carcinoma
MONDO:0007865	knuckle pads
MONDO:0032821	myopathy, congenital, progressive, with scoliosis
MONDO:0007866	Bart-Pumphrey syndrome
MONDO:0005205	systemic lupus erythematosus
MONDO:0032822	developmental and epileptic encephalopathy, 80
MONDO:0007863	Kleine-Levin syndrome
MONDO:0020841	neurodevelopmental disorder with cerebellar atrophy and with or without seizures
MONDO:0005200	viral dilated cardiomyopathy
MONDO:0007864	angioosteohypertrophic syndrome
MONDO:0020840	pulmonary alveolar proteinosis with hypogammaglobulinemia
MONDO:0005202	atopic IgE-mediated allergic disorder
MONDO:0007861	isolated cloverleaf skull syndrome
MONDO:0005201	restrictive cardiomyopathy
MONDO:0007862	Waardenburg syndrome type 3
MONDO:0007860	focal palmoplantar and gingival keratoderma
MONDO:0032829	neurodevelopmental disorder with hypotonia and variable intellectual and behavioral abnormalities
MONDO:0020838	anterior nasal diphtheria
MONDO:0020837	oocyte maturation defect 5
MONDO:0019859	congenital thyroid malformation without hypothyroidism
MONDO:0044807	inherited dystonia
MONDO:0020836	autism, susceptiblity to
MONDO:0020835	methemoglobinemia, alpha type
MONDO:0019856	primary congenital hypothyroidism without thyroid developmental anomaly
MONDO:0044800	desmoplastic spitz nevus
MONDO:0019855	athyreosis
MONDO:0019858	idiopathic congenital hypothyroidism
MONDO:0019857	congenital hypothyroidism due to transplacental passage of maternal TSH-binding inhibitory antibodies
MONDO:0020831	congenital vertebral-cardiac-renal anomalies syndrome
MONDO:0019852	inherited primary ovarian failure
MONDO:0032830	snijders blok-fisher syndrome
MONDO:0032831	pontocerebellar hypoplasia, type 13
MONDO:0019851	acquired primary ovarian failure
MONDO:0019854	thyroid ectopia
MONDO:0019853	congenital hypothyroidism due to developmental anomaly
MONDO:0044808	early onset primary dystonia
MONDO:0019850	precocious puberty
MONDO:0032838	neurodevelopmental disorder with microcephaly, arthrogryposis, and structural brain anomalies
MONDO:0005219	breast fibrocystic disease
MONDO:0032839	noonan syndrome 12
MONDO:0005218	muscular disease
MONDO:0032836	weiss-kruszka syndrome
MONDO:0032837	abdominal obesity-metabolic syndrome 4
MONDO:0007878	congenital laryngomalacia
MONDO:0005215	vulvar carcinoma
MONDO:0032834	retinitis pigmentosa 86
MONDO:0007879	larynx atresia
MONDO:0005214	vulva sarcoma
MONDO:0032835	spondyloepiphyseal dysplasia, nishimura type
MONDO:0007876	laryngeal abductor paralysis
MONDO:0005217	familial cardiomyopathy
MONDO:0032832	intellectual developmental disorder with nasal speech, dysmorphic facies, and variable skeletal anomalies
MONDO:0005216	hypopharyngeal carcinoma
MONDO:0007877	laryngeal adductor paralysis
MONDO:0032833	lower urinary tract obstruction, congenital
MONDO:0005211	ovarian serous adenocarcinoma
MONDO:0007874	trichorhinophalangeal syndrome type II
MONDO:0020830	diaphragmitis
MONDO:0005210	uterine corpus sarcoma
MONDO:0007875	Larsen syndrome
MONDO:0007872	LADD syndrome
MONDO:0005213	uterine carcinoma
MONDO:0007873	lactic acidosis, chronic adult form
MONDO:0005212	rhabdomyosarcoma
MONDO:0007870	labia minora, incomplete adhesion of
MONDO:0007871	familial congenital nasolacrimal duct obstruction
MONDO:0044816	familial idiopathic torsion dystonia
MONDO:0019849	isolated micropenis
MONDO:0019848	posterior hypospadias
MONDO:0044817	acquired idiopathic torsion dystonia
MONDO:0020823	infantile miliaria
MONDO:0019845	iatrogenic or traumatic pituitary deficiency
MONDO:0019844	pituitary hormone deficiency secondary to storage disease
MONDO:0044811	idiopathic torsion dystonia
MONDO:0019847	congenital adrenal hypoplasia of maternal cause
MONDO:0019846	acquired central diabetes insipidus
MONDO:0020820	distal arthrogryposis type 2B1
MONDO:0019841	pituitary hormone defiency from vascular origin
MONDO:0032841	Usher syndrome, type 1M
MONDO:0032842	siddiqi syndrome
MONDO:0019840	acropectororenal dysplasia
MONDO:0019843	pituitary hormone deficiency secondary to a granulomatous disease
MONDO:0019842	pituitary apoplexy
MONDO:0032849	neurodevelopmental disorder with spastic quadriplegia, optic atrophy, seizures, and structural brain anomalies
MONDO:0007849	keratitis fugax hereditaria
MONDO:0056816	vulvar neuroendocrine carcinoma
MONDO:0056817	rectal adenosquamous carcinoma
MONDO:0056818	skin adenosquamous carcinoma
MONDO:0007847	keloid formation
MONDO:0007848	autosomal dominant keratitis
MONDO:0032848	immunodeficiency 65, susceptibility to viral infections
MONDO:0056819	nasal cavity and paranasal sinus carcinoma
MONDO:0032845	spermatogenic failure 39
MONDO:0007845	Kaposi sarcoma, susceptibility to
MONDO:0007846	KBG syndrome
MONDO:0056813	hormone-resistant breast carcinoma
MONDO:0032846	osteogenesis imperfecta, type 20
MONDO:0056814	hormone-resistant prostate carcinoma
MONDO:0007843	Kabuki syndrome 1
MONDO:0032843	oculopharyngeal myopathy with leukoencephalopathy 1
MONDO:0032844	infantile liver failure syndrome 3
MONDO:0007844	hypogonadotropic hypogonadism 2 with or without anosmia
MONDO:0056815	liver adenosquamous carcinoma
MONDO:0007841	coxopodopatellar syndrome
MONDO:0007842	Ehlers-Danlos syndrome type 11
MONDO:0007840	internal carotid artery, spontaneous dissection of
MONDO:0020816	miliaria papulosa
MONDO:0019838	adenohypophysitis
MONDO:0020815	dentigerous cyst
MONDO:0019837	atrial appendage anomaly
MONDO:0020814	miliaria alba
MONDO:0020813	benign testicular sertoli cell tumor
MONDO:0019839	panhypophysitis
MONDO:0019834	pituitary hormone deficiency from meningeal origin
MONDO:0020812	exposure, dental pulp
MONDO:0019833	pituitary hormone deficiency from tumoral origin
MONDO:0020811	mitochondrial complex III deficiency, nuclear type
MONDO:0019836	congenital anomaly of hepatic vein
MONDO:0020810	congenital multiple café-au-lait macules-increased sister chromatid exchange syndrome
MONDO:0019835	primary hypophysitis
MONDO:0019830	congenital anomaly of the inferior vena cava
MONDO:0032852	myopathy, congenital, with structured cores and z-line abnormalities
MONDO:0032853	myopathy, distal, 6, adult-onset, autosomal dominant
MONDO:0056820	nasal cavity and paranasal sinus neoplasm
MONDO:0056821	bronchiolitis obliterans organizing pneumonia
MONDO:0019832	acquired pituitary hormone deficiency
MONDO:0032850	neurooculocardiogenitourinary syndrome
MONDO:0019831	congenital anomaly of the coronary sinus
MONDO:0032851	intellectual developmental disorder with impaired language and dysmorphic facies
MONDO:0056822	amyotonia congenita
MONDO:0020818	secondary dentine
MONDO:0020817	miliaria vesiculosa
MONDO:0056805	benign peripheral nerve granular cell tumor
MONDO:0056806	non-small cell squamous lung carcinoma
MONDO:0007858	palmoplantar keratoderma, punctate type 1A
MONDO:0032858	developmental and epileptic encephalopathy, 81
MONDO:0007859	palmoplantar keratoderma i, striate, focal, or diffuse
MONDO:0032859	spermatogenic failure 40
MONDO:0007856	palmoplantar keratoderma-esophageal carcinoma syndrome
MONDO:0056802	synovial bursa disease
MONDO:0032857	diarrhea 11, malabsorptive, congenital
MONDO:0007857	keratosis palmaris et plantaris-clinodactyly syndrome
MONDO:0007854	keratolytic winter erythema
MONDO:0056803	sulfur metabolism disease
MONDO:0032854	zimmermann-laband syndrome 3
MONDO:0032855	neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies
MONDO:0007855	keratosis, familial actinic
MONDO:0056804	benign neoplasm of peripheral nervous system
MONDO:0007852	palmoplantar keratoderma-deafness syndrome
MONDO:0007853	palmoplantar keratoderma-hereditary motor and sensory neuropathy syndrome
MONDO:0007850	autosomal dominant keratitis-ichthyosis-deafness syndrome
MONDO:0044843	torsion dystonia
MONDO:0007851	keratoconus 1
MONDO:0019819	double-orifice mitral valve
MONDO:0020805	benign basal cell neoplasm
MONDO:0019827	disease associated with non-acquired combined pituitary hormone deficiency
MONDO:0020804	basal cell carcinoma
MONDO:0019826	abnormal origin or aberrant course of coronary artery
MONDO:0019829	congenital anomaly of superior vena cava
MONDO:0020803	bundle branch block
MONDO:0019828	pituitary stalk interruption syndrome
MONDO:0020802	basal cell cancer
MONDO:0019823	premature closure of the arterial duct
MONDO:0020801	rectal medullary carcinoma
MONDO:0020800	demyelinating disease of central nervous system
MONDO:0019822	arterial duct anomaly
MONDO:0019825	congenital coronary artery aneurysm
MONDO:0019824	non-acquired pituitary hormone deficiency
MONDO:0032863	spermatogenic failure 41
MONDO:0032864	intellectual developmental disorder with speech delay, autism, and dysmorphic facies
MONDO:0019821	aneurysm or dilatation of ascending aorta
MONDO:0019820	univentricular cardiopathy
MONDO:0032862	hydrocephalus, congenital communicating, 1
MONDO:0020809	benign sertoli cell tumor
MONDO:0032860	intellectual developmental disorder, autosomal recessive 72
MONDO:0020808	testicular sertoli cell tumor
MONDO:0020807	ovarian sertoli-stromal cell tumor
MONDO:0020806	sinoatrial block
MONDO:0019890	non-distal trisomy 9q
MONDO:0005247	bacterial urinary tract infection
MONDO:0005249	pneumonia
MONDO:0005244	peripheral neuropathy
MONDO:0005243	Cushing syndrome
MONDO:0005246	osteomyelitis
MONDO:0005245	testicular seminoma
MONDO:0005240	kidney disease
MONDO:0005242	empyema
MONDO:0005241	adrenocortical carcinoma
MONDO:0017237	hereditary sensorimotor neuropathy with hyperelastic skin
MONDO:0017238	hemoglobinopathy Toms River
MONDO:0019899	distal monosomy 20q
MONDO:0017239	familial progressive hyper- and hypopigmentation
MONDO:0019896	Kleefstra syndrome due to 9q34 microdeletion
MONDO:0017233	familial Alzheimer-like prion disease
MONDO:0017234	inherited prion disease
MONDO:0019895	distal monosomy 4q
MONDO:0019898	distal monosomy 14q
MONDO:0017235	familial omphalocele syndrome with facial dysmorphism
MONDO:0019897	distal monosomy 12q
MONDO:0017236	rapidly progressive glomerulonephritis
MONDO:0019892	distal monosomy 7p
MONDO:0019891	monosomy 22
MONDO:0017230	autosomal semi-dominant severe lipodystrophic laminopathy
MONDO:0019894	non-distal monosomy 7p
MONDO:0017231	erythropoietic uroporphyria associated with myeloid malignancy
MONDO:0017232	recessive intellectual disability-motor dysfunction-multiple joint contractures syndrome
MONDO:0019893	distal monosomy 19p13.3
MONDO:0005259	Asperger syndrome
MONDO:0005258	autism spectrum disorder
MONDO:0005255	mild heart failure
MONDO:0005254	symptomatic heart failure
MONDO:0005257	advanced heart failure
MONDO:0020871	name syndrome
MONDO:0005256	moderate heart failure
MONDO:0005251	pauciarticular juvenile rheumatoid arthritis
MONDO:0005250	placental villitis
MONDO:0005253	high output heart failure
MONDO:0005252	heart failure
MONDO:0017226	Pelizaeus-Merzbacher-like disease
MONDO:0019889	distal trisomy 22q
MONDO:0017227	autoimmune pancreatitis type 1
MONDO:0019888	distal trisomy 20q
MONDO:0020866	nasopharyngeal diphtheria
MONDO:0017228	autoimmune pancreatitis type 2
MONDO:0017229	distal monosomy 12p
MONDO:0017222	Pelizaeus-Merzbacher disease, classic form
MONDO:0019885	distal trisomy 11q
MONDO:0017223	Pelizaeus-Merzbacher disease, transitional form
MONDO:0019884	distal trisomy 10q
MONDO:0017224	Pelizaeus-Merzbacher disease in female carriers
MONDO:0019887	distal trisomy 16q
MONDO:0019886	distal trisomy 13q
MONDO:0017225	null syndrome
MONDO:0019881	distal trisomy 6q
MONDO:0019880	distal trisomy 5q
MONDO:0019883	distal trisomy 9q
MONDO:0017220	laryngotracheoesophageal cleft type 0
MONDO:0017221	Pelizaeus-Merzbacher disease, connatal form
MONDO:0019882	distal trisomy 8q
MONDO:0032805	hypopigmentation, organomegaly, and delayed myelination and development
MONDO:0032806	trichothiodystrophy 7, nonphotosensitive
MONDO:0005229	bacterial infectious disease with sepsis
MONDO:0032803	immunodeficiency 64
MONDO:0032804	ectodermal dysplasia 15, hypohidrotic/hair type
MONDO:0007889	lentigines
MONDO:0005226	acute basophilic leukemia
MONDO:0032801	erythrokeratodermia variabilis et progressiva 6
MONDO:0032802	deafness, autosomal dominant 37
MONDO:0005225	acute myeloblastic leukemia with maturation
MONDO:0007887	leiomyoma of vulva and esophagus
MONDO:0005228	anaplastic large cell lymphoma
MONDO:0005227	abscess
MONDO:0007888	hereditary leiomyomatosis and renal cell cancer
MONDO:0032800	robinow syndrome, autosomal recessive 2
MONDO:0007885	Legg-Calve-Perthes disease
MONDO:0020863	laryngeal diphtheria
MONDO:0005222	acute megakaryoblastic leukaemia
MONDO:0007886	uterine corpus leiomyoma
MONDO:0005221	renal pelvis urothelial carcinoma
MONDO:0005224	acute myeloblastic leukemia without maturation
MONDO:0007883	periodic fever, immunodeficiency, and thrombocytopenia syndrome
MONDO:0007884	leg ulcers, familial, of juvenile onset
MONDO:0020860	faucial diphtheria
MONDO:0005223	acute myeloid leukemia with minimal differentiation
MONDO:0007881	tooth agenesis, selective, 4
MONDO:0032809	hepatitis, fulminant viral, susceptibility to
MONDO:0007882	lattice degeneration of retina leading to retinal detachment
MONDO:0005220	collecting duct carcinoma
MONDO:0032807	neurodevelopmental disorder with visual defects and brain anomalies
MONDO:0007880	congenital laryngeal web
MONDO:0032808	developmental and epileptic encephalopathy, 77
MONDO:0017219	microform holoprosencephaly
MONDO:0020858	mitochondrial complex 5 (ATP synthase) deficiency nuclear type 5
MONDO:0020857	ovarian dysgenesis 7
MONDO:0020856	bone marrow failure syndrome 4
MONDO:0017215	calciphylaxis
MONDO:0019878	3q26 microduplication syndrome
MONDO:0019877	distal trisomy 2q
MONDO:0017216	calciphylaxis cutis
MONDO:0020855	spermatogenic failure 32
MONDO:0017217	visceral calciphylaxis
MONDO:0020854	Liddle syndrome 2
MONDO:0017218	septopreoptic holoprosencephaly
MONDO:0019879	distal trisomy 4q
MONDO:0020853	encephalitis/encephalopathy, mild, with reversible myelin vacuolization
MONDO:0019874	distal trisomy 7p
MONDO:0017211	infectious panuveitis
MONDO:0017212	paraneoplastic uveitis
MONDO:0019873	4p16.3 microduplication syndrome
MONDO:0017213	postorgasmic illness syndrome
MONDO:0019876	8p inverted duplication/deletion syndrome
MONDO:0019875	Beckwith-Wiedemann syndrome due to 11p15 microduplication
MONDO:0017214	vitamin B12-responsive methylmalonic acidemia
MONDO:0019870	distal trisomy 1p36
MONDO:0019872	distal trisomy 3p
MONDO:0019871	distal trisomy 2p
MONDO:0017210	infectious anterior uveitis
MONDO:0032816	neurodevelopmental disorder with ataxia, hypotonia, and microcephaly
MONDO:0032817	neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies
MONDO:0032814	microangiopathy and leukoencephalopathy, pontine, autosomal dominant
MONDO:0032815	mitochondrial DNA depletion syndrome 17
MONDO:0005237	pleomorphic liposarcoma
MONDO:0032812	developmental and epileptic encephalopathy, 78
MONDO:0005236	xanthoma
MONDO:0032813	developmental and epileptic encephalopathy, 79
MONDO:0007898	leukocyte nuclear appendages, hereditary prevalence of
MONDO:0032810	oocyte maturation defect 7
MONDO:0005239	dedifferentiated liposarcoma
MONDO:0007899	lichen sclerosus et atrophicus
MONDO:0032811	night blindness, congenital stationary, type1i
MONDO:0005238	round cell liposarcoma
MONDO:0007896	acute monocytic leukemia
MONDO:0005233	non-small cell lung carcinoma
MONDO:0020852	spermatogenic failure 31
MONDO:0020851	spermatogenic failure 30
MONDO:0005232	large cell carcinoma
MONDO:0007897	leukemia, chronic lymphocytic
MONDO:0007894	Leri pleonosteosis
MONDO:0020850	intellectual disability, autosomal recessive 65
MONDO:0005235	smoldering plasma cell myeloma
MONDO:0007895	platyspondylic dysplasia, Torrance type
MONDO:0005234	polymyositis
MONDO:0007892	Lenz-Majewski hyperostotic dwarfism
MONDO:0007893	Noonan syndrome with multiple lentigines
MONDO:0005231	hepatitis C virus infection
MONDO:0007890	lentiginosis, centrofacial neurodysraphic
MONDO:0032818	neurodevelopmental disorder with cerebellar hypoplasia and spasticity
MONDO:0005230	cellulitis
MONDO:0007891	familial generalized lentiginosis
MONDO:0032819	hypothyroidism, congenital, nongoitrous, 7
MONDO:0020849	immunodeficiency 57
MONDO:0017208	intermediate uveitis
MONDO:0017209	infectious posterior uveitis
MONDO:0020848	osteopetrosis, autosomal dominant 3
MONDO:0020847	intellectual disability, autosomal dominant 58
MONDO:0020846	intellectual disability, autosomal recessive 64
MONDO:0020845	progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 5
MONDO:0019867	mosaic trisomy 8
MONDO:0017204	toxic maculopathy due to antimalarial drugs
MONDO:0019866	mosaic trisomy 5
MONDO:0017205	primary oculocerebral lymphoma
MONDO:0019869	mosaic trisomy 22
MONDO:0020843	pseudomembranous diphtheritic conjunctivitis
MONDO:0017207	primary organ-specific lymphoma
MONDO:0019868	mosaic trisomy 10
MONDO:0020842	medullary carcinoma
MONDO:0019863	acro-renal-ocular syndrome
MONDO:0017200	polycystic ovaries-urethral sphincter dysfunction syndrome
MONDO:0019862	levocardia
MONDO:0017201	Spasmus nutans
MONDO:0032820	neurodevelopmental disorder with structural brain anomalies and dysmorphic facies
MONDO:0017202	acute endophthalmitis
MONDO:0019865	mosaic trisomy 4
MONDO:0017203	chronic endophthalmitis
MONDO:0019864	tetrasomy 21
MONDO:0019861	thyroid hypoplasia
MONDO:0019860	thyroid hemiagenesis
MONDO:0007827	inclusion body myositis
MONDO:0007828	indifference to pain, congenital, autosomal dominant
MONDO:0007825	incisors, rotation of upper central
MONDO:0007826	incisors, shovel-shaped
MONDO:0007823	insulin receptors, familial increase 1N
MONDO:0007824	incisors, lower central, absence of
MONDO:0007821	immunoglobulin switch sequences
MONDO:0007822	incisors, long upper central
MONDO:0007820	fused mandibular incisors
MONDO:0019809	congenital aortic valve insufficiency
MONDO:0019808	aortic valve atresia
MONDO:0019816	anomaly of the tricuspid subvalvular apparatus
MONDO:0019815	accessory tricuspid valve tissue
MONDO:0019818	cleft mitral valve
MONDO:0019817	congenital mitral valve insufficiency and/or stenosis
MONDO:0019812	tricuspid valve prolapse
MONDO:0019811	tricuspid valve agenesis
MONDO:0019814	straddling or overriding tricuspid valve
MONDO:0019813	congenital tricuspid stenosis
MONDO:0019810	toxic epidermal necrolysis
MONDO:0007818	Hyper-IgE recurrent infection syndrome 1
MONDO:0007819	solitary median maxillary central incisor syndrome
MONDO:0007838	Jacobsen syndrome
MONDO:0007839	Aase-Smith syndrome
MONDO:0007836	IVIC syndrome
MONDO:0007837	Johnson neuroectodermal syndrome
MONDO:0007834	islet cell adenomatosis
MONDO:0007835	intussusception
MONDO:0007832	interferon antiviral depressor
MONDO:0007833	iris pigment layer, cleavage of
MONDO:0007830	insensitivity to pain with hyperplastic Myelinopathy
MONDO:0007831	insect Stings, hypersensitivity to
MONDO:0019805	twin to twin transfusion syndrome
MONDO:0019804	tracheomalacia
MONDO:0019807	mesocardia
MONDO:0019806	primary progressive aphasia
MONDO:0019801	acute adrenal insufficiency
MONDO:0019800	chronic hepatic porphyria
MONDO:0019803	angioma serpiginosum
MONDO:0019802	secondary short bowel syndrome
MONDO:0007829	cholestasis, intrahepatic, of pregnancy, 1
MONDO:0007805	hypotrichosis 2
MONDO:0007806	hypotrichosis 4
MONDO:0007803	multiple system atrophy
MONDO:0007804	Pallister-hall syndrome
MONDO:0007801	hypoplasia of teeth roots
MONDO:0007802	hypospadias 3, autosomal
MONDO:0007800	chromosome 18p deletion syndrome
MONDO:0007816	immune suppression
MONDO:0007817	IgE responsiveness, atopic
MONDO:0007814	immune deficiency, familial variable
MONDO:0007815	immunodeficiency with defective leukocyte and lymphocyte function and with response to histamine-1 antagonist
MONDO:0007812	ichthyosis, lamellar, autosomal dominant
MONDO:0007813	ichthyosis bullosa of Siemens
MONDO:0007810	autosomal dominant ichthyosis vulgaris
MONDO:0007811	ichthyosis-cheek-eyebrow syndrome
MONDO:0007809	ichthyosis hystrix gravior
MONDO:0007807	hypoxanthine guanine phosphoribosyltransferase suppressor
MONDO:0007808	ichthyosis hystrix of Curth-Macklin
MONDO:0017093	unilateral focal polymicrogyria
MONDO:0017094	cerebral cortical dysplasia
MONDO:0017095	isolated focal cortical dysplasia type I
MONDO:0017096	isolated focal cortical dysplasia type Ia
MONDO:0017090	midline cerebral malformation
MONDO:0017091	bilateral polymicrogyria
MONDO:0017092	unilateral polymicrogyria
MONDO:0017097	isolated focal cortical dysplasia type Ib
MONDO:0017098	isolated focal cortical dysplasia type Ic
MONDO:0017099	facioscapulohumeral dystrophy
MONDO:0017082	basal encephalocele
MONDO:0017083	lipoma associated with neurospinal dysraphism
MONDO:0017084	leptomyelolipoma
MONDO:0017085	malformation of the neurenteric canal, spinal cord and column
MONDO:0017080	occipital encephalocele
MONDO:0017081	parietal encephalocele
MONDO:0017086	primary tethered cord syndrome
MONDO:0017087	neurenteric cyst
MONDO:0017088	isolated amyelia
MONDO:0017089	isolated megalencephaly
MONDO:0044690	optic perineuritis
MONDO:0030049	46,xx sex reversal 5
MONDO:0044699	SIN3A-related intellectual disability syndrome
MONDO:0044696	early-onset progressive encephalopathy-hearing loss-pons hypoplasia-brain atrophy syndrome
MONDO:0030051	intellectual developmental disorder with autistic features and language delay, with or without seizures
MONDO:0030057	neurodevelopmental, jaw, eye, and digital syndrome
MONDO:0030056	Fanconi renotubular syndrome 5
MONDO:0030059	developmental and epileptic encephalopathy, 87
MONDO:0030058	deafness, autosomal dominant 77
MONDO:0030055	sorbitol dehydrogenase deficiency with peripheral neuropathy
MONDO:0030054	developmental and epileptic encephalopathy, 86
MONDO:0030060	neurodevelopmental disorder with language impairment and behavioral abnormalities
MONDO:0030062	arrhythmogenic right ventricular dysplasia, familial, 14
MONDO:0030061	periventricular nodular heterotopia 9
MONDO:0030067	treacher collins syndrome 4
MONDO:0030069	hyper-IgE recurrent infection syndrome 5, autosomal recessive
MONDO:0030064	episodic ataxia, type 9
MONDO:0030063	neurodevelopmental disorder with seizures, hypotonia, and brain imaging abnormalities
MONDO:0030066	granulomatous disease, chronic, autosomal recessive, 5
MONDO:0030065	agenesis of corpus callosum, cardiac, ocular, and genital syndrome
MONDO:0030071	retinitis pigmentosa 89
MONDO:0030070	heterotaxy, visceral, 9, autosomal, with male infertility
MONDO:0030073	Mitchell syndrome
MONDO:0030072	developmental and epileptic encephalopathy, 88
MONDO:0030074	spondylometaphyseal dysplasia with corneal dystrophy
MONDO:0030077	vertebral, cardiac, renal, and limb defects syndrome 3
MONDO:0030089	diabetes mellitus, permanent neonatal 4
MONDO:0030088	diabetes mellitus, permanent neonatal 3
MONDO:0030087	diabetes mellitus, permanent neonatal 2
MONDO:0019690	filamin-related bone disorder
MONDO:0030009	alopecia-intellectual disability syndrome 4
MONDO:0019692	multiple epiphyseal dysplasia and pseudoachondroplasia
MONDO:0019691	short rib dysplasia
MONDO:0017030	interstitial lung disease in childhood and adulthood
MONDO:0030006	combined oxidative phosphorylation deficiency 40
MONDO:0032669	Diamond-Blackfan anemia 19
MONDO:0005049	intracranial hemorrhage
MONDO:0030005	epilepsy, early-onset, with or without developmental delay
MONDO:0032667	epidermodysplasia verruciformis, susceptibility to, 5
MONDO:0030008	combined oxidative phosphorylation deficiency 42
MONDO:0032668	Diamond-Blackfan anemia 18
MONDO:0030007	combined oxidative phosphorylation deficiency 41
MONDO:0005046	immune system disease
MONDO:0020687	supratentorial ependymal tumor
MONDO:0005045	hypertrophic cardiomyopathy
MONDO:0020686	acute tonsillitis
MONDO:0044656	epidermolytic nevus
MONDO:0005048	pancreatic insulin-producing neuroendocrine tumor
MONDO:0020685	infratentorial ependymal tumor
MONDO:0005047	infertility disorder
MONDO:0020684	Ehlers-Danlos syndrome, periodontal type 1
MONDO:0044655	c12orf65-related combined oxidative phosphorylation defect
MONDO:0020683	acute disease
MONDO:0005042	head disease
MONDO:0005041	glaucoma
MONDO:0020682	Ehlers-Danlos syndrome, progeroid type 1
MONDO:0020681	Ehlers-Danlos syndrome, musculocontractural type 1
MONDO:0005044	hypertensive disorder
MONDO:0044652	optic atrophy-peripheral neuropathy-developmental delay syndrome
MONDO:0005043	hyperplasia
MONDO:0020680	acute bronchiolitis
MONDO:0044651	early-onset progressive encephalopathy-spastic ataxia-distal spinal muscular atrophy syndrome
MONDO:0005040	germ cell tumor
MONDO:0017039	drug or radiation exposure-related interstitial lung disease
MONDO:0044647	kyphosis-lateral tongue atrophy-myofibrillar myopathy syndrome
MONDO:0044646	early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome
MONDO:0020679	conductive hearing loss disorder
MONDO:0044649	omphalocele-diaphragmatic hernia-cardiovascular anomalies-radial ray defect syndrome
MONDO:0020678	sensorineural hearing loss disorder
MONDO:0020677	sudden hearing loss disorder
MONDO:0044648	kyphoscoliosis-lateral tongue atrophy-hereditary spastic paraplegia syndrome
MONDO:0030013	immunodeficiency 66
MONDO:0017035	secondary interstitial lung disease in childhood and adulthood associated with a systemic disease
MONDO:0019698	bent bone dysplasia
MONDO:0030012	Diets-Jongmans syndrome
MONDO:0032677	lissencephaly 9 with complex brainstem malformation
MONDO:0019697	mesomelic and rhizo-mesomelic dysplasia
MONDO:0017036	Langerhans cell histiocytosis in childhood and adulthood
MONDO:0017037	secondary interstitial lung disease in childhood and adulthood associated with a metabolic disease
MONDO:0030015	bone marrow failure syndrome 6
MONDO:0017038	secondary interstitial lung disease in childhood and adulthood associated with a systemic vasculitis
MONDO:0030014	muscular dystrophy, limb-girdle, autosomal recessive 26
MONDO:0019699	slender bone dysplasia
MONDO:0032675	myasthenic syndrome, congenital, 25, presynaptic
MONDO:0017031	primary interstitial lung disease in childhood and adulthood
MONDO:0032672	intellectual developmental disorder with cardiac defects and dysmorphic facies
MONDO:0019694	spondylodysplastic dysplasia
MONDO:0019693	multiple metaphyseal dysplasia
MONDO:0017032	primary interstitial lung disease in childhood and adulthood due to alveolar structure disorder
MONDO:0032673	basal ganglia calcification, idiopathic, 7, autosomal recessive
MONDO:0032670	Diamond-Blackfan anemia 20
MONDO:0019696	acromesomelic dysplasia
MONDO:0017033	primary interstitial lung disease in childhood and adulthood due to alveolar vascular disorder
MONDO:0019695	acromelic dysplasia
MONDO:0030010	hypogonadotropic hypogonadism 25 with anosmia
MONDO:0017034	secondary interstitial lung disease in childhood and adulthood
MONDO:0019681	juvenile sialidosis type 2
MONDO:0019680	genochondromatosis type 2
MONDO:0030017	combined oxidative phosphorylation deficiency 43
MONDO:0032678	developmental and epileptic encephalopathy, 71
MONDO:0030019	anauxetic dysplasia 3
MONDO:0032679	combined oxidative phosphorylation deficiency 37
MONDO:0030018	autoinflammation with episodic fever and lymphadenopathy
MONDO:0005057	large cell neuroendocrine carcinoma
MONDO:0020676	disease of central nervous system or retinal vasculature
MONDO:0029001	chemically-induced disorder
MONDO:0005056	keratinizing squamous cell carcinoma
MONDO:0020675	ischemic bowel disease
MONDO:0005059	leukemia
MONDO:0029000	poisoning
MONDO:0020674	vascular insufficiency disorder
MONDO:0020673	arterial occlusion
MONDO:0005058	leiomyosarcoma
MONDO:0005053	ischemic disease
MONDO:0020672	vascular occlusion disorder
MONDO:0005052	irritable bowel syndrome
MONDO:0020671	susceptibility to ischemic stroke
MONDO:0044660	menstrual cycle-dependent periodic fever
MONDO:0005055	Kaposi's sarcoma
MONDO:0020670	antithrombin deficiency type 2
MONDO:0044663	aquagenic palmoplantar keratoderma
MONDO:0005054	juvenile dermatomyositis
MONDO:0032680	global developmental delay with or without impaired intellectual development
MONDO:0005051	invasive lobular breast carcinoma
MONDO:0005050	invasive ductal and lobular carcinoma
MONDO:0020669	paranasal sinus cancer
MONDO:0017028	secondary interstitial lung disease specific to adulthood associated with a systemic disease
MONDO:0044657	MME-related autosomal dominant Charcot Marie Tooth disease type 2
MONDO:0020668	spastic paraplegia 5B
MONDO:0017029	Langerhans cell histiocytosis specific to adulthood
MONDO:0020667	Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis
MONDO:0020666	Löfgren syndrome
MONDO:0032687	intellectual developmental disorder with abnormal behavior, microcephaly, and short stature
MONDO:0030024	neurodevelopmental disorder with or without autistic features and/or structural brain abnormalities
MONDO:0017024	secondary interstitial lung disease specific to childhood associated with a metabolic disease
MONDO:0019687	type 11 collagen-related bone disorder
MONDO:0032688	polymicrogyria with or without vascular-type ehlers-danlos syndrome
MONDO:0017025	Langerhans cell histiocytosis specific to childhood
MONDO:0019686	type 2 collagen-related bone disorder
MONDO:0032685	infantile cataract, skin abnormalities, glutamate excess, and impaired intellectual development
MONDO:0017026	interstitial lung disease specific to adulthood
MONDO:0030026	retinal dystrophy with leukodystrophy
MONDO:0019689	perlecan-related bone disorder
MONDO:0017027	primary interstitial lung disease specific to adulthood
MONDO:0019688	sulfation-related bone disorder
MONDO:0032686	spermatogenic failure 35
MONDO:0030025	neurodevelopmental disorder with hypotonia, microcephaly, and seizures
MONDO:0017020	secondary interstitial lung disease specific to childhood associated with a systemic disease
MONDO:0030020	combined oxidative phosphorylation deficiency 44
MONDO:0019683	syndactyly type 2
MONDO:0032684	intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, genital anomalies, and immunodeficiency
MONDO:0017021	secondary interstitial lung disease specific to childhood associated with a connective tissue disease
MONDO:0019682	congenital sialidosis type 2
MONDO:0032681	encephalopathy, progressive, early-onset, with episodic rhabdomyolysis
MONDO:0019685	FGFR3-related chondrodysplasia
MONDO:0017022	secondary interstitial lung disease specific to childhood associated with a systemic vasculitis
MONDO:0017023	secondary interstitial lung disease specific to childhood associated with a granulomatous disease
MONDO:0019684	rare bone disease
MONDO:0019670	ulnar hemimelia
MONDO:0005028	esophageal adenocarcinoma
MONDO:0030028	neurodegeneration, childhood-onset, with ataxia, tremor, optic atrophy, and cognitive decline
MONDO:0005027	epilepsy
MONDO:0030027	tremor, hereditary essential, 6
MONDO:0007689	guanylate kinase 3
MONDO:0032689	retinitis pigmentosa 85
MONDO:0005029	essential thrombocythemia
MONDO:0030029	skeletal dysplasia, mild, with joint laxity and advanced bone age
MONDO:0020665	high grade malignant neoplasm
MONDO:0007687	graying of hair, precocious
MONDO:0005024	emphysema
MONDO:0005023	ductal breast carcinoma in situ
MONDO:0020664	spindle cell neoplasm
MONDO:0007688	Myhre syndrome
MONDO:0044675	LRP5-related primary osteoporosis
MONDO:0005026	endometrioid adenocarcinoma
MONDO:0007685	granulosis rubra nasi
MONDO:0020663	malignant spindle cell neoplasm
MONDO:0007686	gray platelet syndrome
MONDO:0005025	endocarditis
MONDO:0020662	borderline ovarian serous tumor
MONDO:0007683	Grant syndrome
MONDO:0005020	intestinal disease
MONDO:0020661	undifferentiated round cell sarcoma
MONDO:0020660	osteoblastic osteosarcoma
MONDO:0007684	granulomatous disease, chronic, autosomal dominant type
MONDO:0007681	goiter, multinodular 1, with or without Sertoli-Leydig cell tumors
MONDO:0005022	ductal breast adenocarcinoma
MONDO:0005021	dilated cardiomyopathy
MONDO:0007682	granddad syndrome
MONDO:0032690	microcephaly, growth deficiency, seizures, and brain malformations
MONDO:0007680	multinodular goiter-cystic kidney-polydactyly syndrome
MONDO:0032691	Galloway-Mowat syndrome 6
MONDO:0020659	upper tract urothelial carcinoma
MONDO:0017017	primary interstitial lung disease specific to childhood due to alveolar vascular disorder
MONDO:0020658	infiltrating ureter transitional cell carcinoma
MONDO:0017018	isolated pulmonary capillaritis
MONDO:0019679	brachydactyly type A7
MONDO:0020657	human papillomavirus-related squamous cell carcinoma
MONDO:0017019	interstitial lung disease specific to infancy
MONDO:0020656	human papillomavirus-related penile squamous cell carcinoma
MONDO:0020655	juvenile ankylosing spondylitis
MONDO:0032698	neurodevelopmental disorder with central and peripheral motor dysfunction
MONDO:0019676	brachydactyly type B
MONDO:0017013	trisomy 8p
MONDO:0030035	leukoencephalopathy, developmental delay, and episodic neurologic regression syndrome
MONDO:0017014	interstitial lung disease specific to childhood
MONDO:0032699	epilepsy, idiopathic generalized, susceptibility to, 15
MONDO:0019675	spondyloepimetaphyseal dysplasia with joint laxity
MONDO:0030034	epilepsy, progressive myoclonic, 11
MONDO:0017015	primary interstitial lung disease specific to childhood
MONDO:0032696	oocyte maturation defect 6
MONDO:0019678	brachydactyly type A5
MONDO:0030037	neurodevelopmental disorder with hypotonia and cerebellar atrophy, with or without seizures
MONDO:0030036	leukoencephalopathy, motor delay, spasticity, and dysarthria syndrome
MONDO:0017016	primary interstitial lung disease specific to childhood due to alveolar structure disorder
MONDO:0032697	neurodevelopmental disorder and language delay with or without structural brain abnormalities
MONDO:0019677	brachydactyly type E
MONDO:0030031	lissencephaly 10
MONDO:0032694	microcephaly 25, primary, autosomal recessive
MONDO:0019672	fibular hemimelia
MONDO:0017010	partial duplication of the long arm of chromosome X
MONDO:0019671	radial hemimelia
MONDO:0030030	Nizon-Isidor syndrome
MONDO:0032692	Galloway-Mowat syndrome 7
MONDO:0019674	postaxial polydactyly type B
MONDO:0017011	uniparental disomy of chromosome X
MONDO:0030033	seizures, early-onset, with neurodegeneration and brain calcifications
MONDO:0017012	partial duplication of the short arm of chromosome 1
MONDO:0019673	postaxial polydactyly type A
MONDO:0032693	Galloway-Mowat syndrome 8
MONDO:0030032	chromosome 17q11.2 duplication syndrome, 1.4-mb
MONDO:0044680	short rib-polydactyly syndrome type 5
MONDO:0005039	reproductive system disease
MONDO:0030038	glaucoma, primary closed-angle
MONDO:0005038	genetic disorder
MONDO:0020654	renal pelvis/ureter urothelial carcinoma
MONDO:0005035	ganglioneuroblastoma
MONDO:0007698	hand-foot-genital syndrome
MONDO:0044687	chronic relapsing inflammatory optic neuropathy
MONDO:0005034	thyroid gland follicular carcinoma
MONDO:0007699	Hashimoto thyroiditis
MONDO:0020653	vaginal adenocarcinoma
MONDO:0005037	gastric intestinal type adenocarcinoma
MONDO:0007696	Emery-Nelson syndrome
MONDO:0044689	recurrent idiopathic neuroretinitis
MONDO:0020652	immature teratoma of vulva
MONDO:0020651	mixed germ cell tumor of vulva
MONDO:0005036	gastric adenocarcinoma
MONDO:0044688	isolated optic neuritis
MONDO:0007697	hand clasping pattern
MONDO:0005031	fibromatosis
MONDO:0007694	hairy nose tip
MONDO:0044683	limbic encephalitis with neurexin-3 antibodies
MONDO:0020650	germ cell tumor of the vulva
MONDO:0007695	hairy palms and soles
MONDO:0005030	fetal growth restriction
MONDO:0044682	MYBPC1-related autosomal recessive non-lethal arthrogryposis multiplex congenita syndrome
MONDO:0005033	ganglioneuroma
MONDO:0007692	hairy ears
MONDO:0044685	autoimmune/inflammatory optic neuropathy
MONDO:0007693	hypertrichosis cubiti-short stature syndrome
MONDO:0044684	tuberculous meningitis
MONDO:0005032	follicular thyroid adenoma
MONDO:0007690	aromatase excess syndrome
MONDO:0007691	Guillain-Barre syndrome, familial
MONDO:0020649	warty carcinoma of the penis
MONDO:0020648	rubella encephalitis
MONDO:0020647	microcephaly, facial dysmorphism, renal agenesis, and ambiguous genitalia syndrome
MONDO:0019669	hypochondrogenesis
MONDO:0017006	X and Y chromosomal anomaly
MONDO:0017007	partial deletion of the long arm of chromosome X
MONDO:0019668	adenoma of pancreas
MONDO:0020646	ocular adnexal lymphoma
MONDO:0020645	autosomal dominant osteopetrosis
MONDO:0017008	partial duplication of chromosome X
MONDO:0017009	partial duplication of the short arm of chromosome X
MONDO:0020644	lung non-Hodgkin lymphoma
MONDO:0030046	neurodevelopmental disorder and structural brain anomalies with or without seizures and spasticity
MONDO:0019665	monostotic fibrous dysplasia
MONDO:0017002	polysomy of X chromosome
MONDO:0019664	short rib-polydactyly syndrome, Verma-Naumoff type
MONDO:0017003	partial deletion of chromosome X
MONDO:0030045	Liberfarb syndrome
MONDO:0019667	spondyloepiphyseal dysplasia tarda
MONDO:0017004	partial monosomy of the short arm of chromosome X
MONDO:0030048	harderoporphyria
MONDO:0019666	spondyloepimetaphyseal dysplasia, PAPSS2 type
MONDO:0030047	microcephaly, developmental delay, and brittle hair syndrome
MONDO:0017005	Y chromosome number anomaly
MONDO:0019661	Pfeiffer syndrome type 3
MONDO:0030042	proteinuria, chronic benign
MONDO:0019660	Pfeiffer syndrome type 2
MONDO:0017000	X chromosome number anomaly with female phenotype
MONDO:0030044	pseudo-TORCH syndrome 3
MONDO:0019663	short rib-polydactyly syndrome, Saldino-Noonan type
MONDO:0019662	short rib-polydactyly syndrome, Majewski type
MONDO:0017001	X chromosome number anomaly with male phenotype
MONDO:0030043	congenital disorder of glycosylation, type iit
MONDO:0032629	mitochondrial complex 1 deficiency, nuclear type 25
MONDO:0017071	thoracolumbosacral spina bifida cystica
MONDO:0017072	lumbosacral spina bifida cystica
MONDO:0017073	cervical spina bifida cystica
MONDO:0032627	mitochondrial complex 1 deficiency, nuclear type 23
MONDO:0017074	cervicothoracic spina bifida cystica
MONDO:0032628	mitochondrial complex 1 deficiency, nuclear type 24
MONDO:0032625	mitochondrial complex 1 deficiency, nuclear type 21
MONDO:0032626	mitochondrial complex 1 deficiency, nuclear type 22
MONDO:0032623	mitochondrial complex 1 deficiency, nuclear type 18
MONDO:0032624	mitochondrial complex 1 deficiency, nuclear type 19
MONDO:0017070	total spina bifida cystica
MONDO:0005089	sarcoma
MONDO:0005086	renal cell carcinoma
MONDO:0005085	pterygium
MONDO:0005088	rheumatoid arthritis
MONDO:0005087	respiratory system disease
MONDO:0005082	prostate adenocarcinoma
MONDO:0005081	preeclampsia
MONDO:0005084	mental disorder
MONDO:0005083	psoriasis
MONDO:0005080	portal hypertension
MONDO:0017079	meningoencephalocele
MONDO:0032632	mitochondrial complex 1 deficiency, nuclear type 28
MONDO:0032633	mitochondrial complex 1 deficiency, nuclear type 29
MONDO:0032630	mitochondrial complex 1 deficiency, nuclear type 26
MONDO:0032631	mitochondrial complex 1 deficiency, nuclear type 27
MONDO:0017075	upper thoracic spina bifida cystica
MONDO:0017076	posterior meningocele
MONDO:0017077	myelocystocele
MONDO:0017078	cephalocele
MONDO:0017060	open iniencephaly
MONDO:0017061	closed iniencephaly
MONDO:0017062	spina bifida aperta
MONDO:0032639	deafness, autosomal recessive 112
MONDO:0017063	total spina bifida aperta
MONDO:0032636	mitochondrial complex 1 deficiency, nuclear type 33
MONDO:0032637	ciliary dyskinesia, primary, 39
MONDO:0032634	mitochondrial complex 1 deficiency, nuclear type 31
MONDO:0032635	mitochondrial complex 1 deficiency, nuclear type 32
MONDO:0044621	16p12.1p12.3 triplication syndrome
MONDO:0044622	EMILIN-1-related connective tissue disease
MONDO:0005097	squamous cell lung carcinoma
MONDO:0005096	squamous cell carcinoma
MONDO:0005099	subarachnoid hemorrhage
MONDO:0005098	stroke disorder
MONDO:0005093	skin disease
MONDO:0044618	CLCN4-related X-linked intellectual disability syndrome
MONDO:0005092	signet ring cell carcinoma
MONDO:0044617	X-linked keloid scarring-reduced joint mobility-increased optic cup-to-disc ratio syndrome
MONDO:0005095	spondyloarthropathy
MONDO:0005094	hemangiopericytoma
MONDO:0044619	propylthiouracil embryofetopathy
MONDO:0029042	ureteropelvic junction obstruction
MONDO:0005091	severe acute respiratory syndrome
MONDO:0005090	schizophrenia
MONDO:0017068	upper thoracic spina bifida aperta
MONDO:0032643	pontocerebellar hypoplasia, type 12
MONDO:0017069	spina bifida cystica
MONDO:0032644	epidermodysplasia verruciformis, susceptibility to, 3
MONDO:0032641	mirror movements 4
MONDO:0032642	arthrogryposis, cleft palate, craniosynostosis, and impaired intellectual development
MONDO:0017064	thoracolumbosacral spina bifida aperta
MONDO:0017065	lumbosacral spina bifida aperta
MONDO:0017066	cervical spina bifida aperta
MONDO:0017067	cervicothoracic spina bifida aperta
MONDO:0017050	intraocular medulloepithelioma
MONDO:0017051	classic maple syrup urine disease
MONDO:0032649	hypotrichosis 14
MONDO:0017052	intermediate maple syrup urine disease
MONDO:0032647	global developmental delay, lung cysts, overgrowth, and wilms tumor
MONDO:0032648	mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations
MONDO:0032645	trichohepatoneurodevelopmental syndrome
MONDO:0032646	congenital anomalies of kidney and urinary tract 3
MONDO:0005068	myocardial infarction
MONDO:0044632	extracranial carotid artery aneurysm
MONDO:0005067	monophasic synovial sarcoma
MONDO:0044631	early-onset familial noncirrhotic portal hypertension
MONDO:0044634	retinitis pigmentosa-hearing loss-premature aging-short stature-facial dysmorphism syndrome
MONDO:0005069	narcolepsy with cataplexy
MONDO:0044633	idiopathic pleuroparenchymal fibroelastosis
MONDO:0005064	infectious meningitis
MONDO:0005063	medullary breast carcinoma
MONDO:0005066	metabolic disease
MONDO:0044630	rere-related neurodevelopmental syndrome
MONDO:0005065	mesothelioma
MONDO:0005060	liposarcoma
MONDO:0044629	congenital amyoplasia
MONDO:0044628	six2-related frontonasal dysplasia
MONDO:0005062	lymphoma
MONDO:0005061	lung adenocarcinoma
MONDO:0044625	autosomal dominant charcot-marie-tooth disease type 2 due to DGAT2 mutation
MONDO:0044624	pediatric collagenous gastritis
MONDO:0044627	acute macular neuroretinopathy
MONDO:0020699	biotin metabolic disease
MONDO:0044626	female infertility due to oocyte meiotic arrest
MONDO:0017057	hereditary thrombocytopenia with normal platelets
MONDO:0032654	hyper-IgE recurrent infection syndrome 3, autosomal recessive
MONDO:0017058	autosomal recessive intermediate Charcot-Marie-Tooth disease
MONDO:0032655	visual impairment and progressive phthisis bulbi
MONDO:0017059	neural tube closure defect
MONDO:0032653	cardiac-urogenital syndrome
MONDO:0017053	intermittent maple syrup urine disease
MONDO:0032650	neurodegeneration, childhood-onset, with cerebellar atrophy
MONDO:0017054	thiamine-responsive maple syrup urine disease
MONDO:0032651	fibrosis, neurodegeneration, and cerebral angiomatosis
MONDO:0017055	mycophenolate mofetil embryopathy
MONDO:0017056	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion
MONDO:0020690	adult glioblastoma
MONDO:0017040	exposure-related interstitial lung disease
MONDO:0017041	osteochondrodysplatic nanism-deafness-retinitis pigmentosa syndrome
MONDO:0032658	macrocephaly, acquired, with impaired intellectual development
MONDO:0032659	mucocutaneous ulceration, chronic
MONDO:0032656	microcephaly, cataracts, impaired intellectual development, and dystonia with abnormal striatum
MONDO:0032657	developmental and epileptic encephalopathy, 69
MONDO:0005079	polyp
MONDO:0020698	inborn error of biotin metabolism
MONDO:0044643	congenital labioscrotal agenesis-cerebellar malformation-corneal dystrophy-facial dysmorphism syndrome
MONDO:0020697	lung epithelial-myoepithelial carcinoma
MONDO:0005078	phyllodes tumor
MONDO:0044642	c11orf73-related autosomal recessive hypomyelinating leukodystrophy
MONDO:0020696	vitamin B12 deficiency
MONDO:0044645	familial monosomy 7 syndrome
MONDO:0044644	congenital agenesis of the scrotum
MONDO:0020695	hypotonic cerebral palsy
MONDO:0005075	thyroid gland papillary carcinoma
MONDO:0020694	salivary gland epithelial myoepithelial carcinoma
MONDO:0005074	papillary cystadenocarcinoma
MONDO:0020693	glycogen storage disease due to liver phosphorylase kinase deficiency
MONDO:0005077	pertussis
MONDO:0020692	spondylocostal dysostosis 1, autosomal recessive
MONDO:0044641	9q33.3q34.11 microdeletion syndrome
MONDO:0044640	charcot-marie-tooth disease type 2T
MONDO:0005076	periodontitis
MONDO:0005071	nervous system disorder
MONDO:0005070	neoplasm
MONDO:0005073	melanocytic nevus
MONDO:0005072	neuroblastoma
MONDO:0044636	rare hyperkinetic movement disorder
MONDO:0044635	diaph1-related sensorineural hearing loss-thrombocytopenia syndrome
MONDO:0044638	hypopharynx squamous cell carcinoma
MONDO:0020689	AIDS dementia complex
MONDO:0020688	spinal cord ischemia
MONDO:0044637	infantile-onset generalized dyskinesia with orofacial involvement
MONDO:0032665	intellectual developmental disorder, autosomal recessive 68
MONDO:0017046	neuroepithelioma
MONDO:0017047	infantile axonal neuropathy
MONDO:0032666	epidermodysplasia verruciformis, susceptibility to, 4
MONDO:0030004	autism, susceptibility to, 20
MONDO:0017048	pseudomyxoma peritonei
MONDO:0032663	developmental and epileptic encephalopathy, 70
MONDO:0017049	hypomyelination neuropathy-arthrogryposis syndrome
MONDO:0032664	ciliary dyskinesia, primary, 40
MONDO:0017042	thanatophoric dysplasia
MONDO:0032661	neurodevelopmental disorder with impaired intellectual development, hypotonia, and ataxia
MONDO:0017043	congenital mesoblastic nephroma
MONDO:0032662	intellectual developmental disorder, autosomal recessive 67
MONDO:0017044	adult familial nephronophthisis-spastic quadriparesia syndrome
MONDO:0032660	spinal muscular atrophy, lower extremity-predominant, 2b, prenatal onset, autosomal dominant
MONDO:0017045	neuroectodermal-endocrine syndrome
MONDO:0032706	spinocerebellar ataxia, autosomal recessive 27
MONDO:0032707	turnpenny-fry syndrome
MONDO:0007748	hypercalciuria, absorptive, 2
MONDO:0007749	autosomal recessive infantile hypercalcemia
MONDO:0032705	neurodevelopmental disorder with microcephaly, epilepsy, and hypomyelination
MONDO:0007746	orthostatic hypotensive disorder, Streeten type
MONDO:0032702	Coffin-Siris syndrome 8
MONDO:0007747	isolated hyperchlorhidrosis
MONDO:0032703	short stature, amelogenesis imperfecta, and skeletal dysplasia with scoliosis
MONDO:0007744	cholesterol-ester transfer protein deficiency
MONDO:0007745	Gilbert syndrome
MONDO:0020720	X-linked hypophosphatemic rickets
MONDO:0007742	5-hydroxytryptamine oxygenase regulator
MONDO:0007743	attention deficit-hyperactivity disorder
MONDO:0007740	Wagner disease
MONDO:0007741	congenital hydronephrosis
MONDO:0019739	atypical hemolytic-uremic syndrome with anti-factor H antibodies
MONDO:0020717	autosomal dominant woolly hair
MONDO:0019738	atypical hemolytic-uremic syndrome with H factor anomaly
MONDO:0020716	familial thyroid dyshormonogenesis 1
MONDO:0020715	Multiple system atrophy 1, susceptibility to
MONDO:0020714	mitochondrial myopathy, episodic, with optic atrophy and reversible leukoencephalopathy
MONDO:0019735	polymyalgia rheumatica
MONDO:0020713	pulmonary venoocclusive disease 1
MONDO:0019734	juvenile polymyositis
MONDO:0020712	46,XY sex reversal 1
MONDO:0019737	thrombotic microangiopathy
MONDO:0020711	selective peripheral resistance to thyroid hormone
MONDO:0019736	dense deposit disease
MONDO:0020710	amnionitis
MONDO:0019731	AApoAI amyloidosis
MONDO:0019730	light chain deposition disease
MONDO:0032710	developmental and epileptic encephalopathy, 72
MONDO:0019733	AFib amyloidosis
MONDO:0019732	ALys amyloidosis
MONDO:0020719	susceptibility to Hirschsprung disease
MONDO:0020718	congenital short bowel syndrome 1
MONDO:0032717	amelogenesis imperfecta, type 3c
MONDO:0007759	hyperlipidemia, familial combined, LPL related
MONDO:0032715	intellectual developmental disorder, autosomal recessive 69
MONDO:0032716	leukoencephalopathy, acute reversible, with increased urinary alpha-ketoglutarate
MONDO:0007757	hyperkeratosis-hyperpigmentation syndrome
MONDO:0007758	epidermolytic palmoplantar keratoderma
MONDO:0032714	facial dysmorphism, hypertrichosis, epilepsy, intellectual/developmental delay, and gingival overgrowth syndrome
MONDO:0007755	hyperimmunoglobulin G1(A1) syndrome
MONDO:0007756	hyperkeratosis lenticularis perstans
MONDO:0032712	combined oxidative phosphorylation deficiency 38
MONDO:0007753	Frey syndrome
MONDO:0007754	hyperhidrosis palmaris ET plantaris
MONDO:0007751	hypercholesterolemia, autosomal dominant, type B
MONDO:0044700	SIN3A-related intellectual disability syndrome due to a point mutation
MONDO:0007752	hyperheparinemia
MONDO:0007750	hypercholesterolemia, familial, 1
MONDO:0019728	heavy chain deposition disease
MONDO:0020706	Heberden's node
MONDO:0020705	neural tube defects, susceptibility to
MONDO:0019727	mixed cryoglobulinemia type III
MONDO:0020704	inherited rippling muscle disease
MONDO:0019729	light and heavy chain deposition disease
MONDO:0020703	erythroid neoplasm
MONDO:0019724	secondary glomerular disease
MONDO:0020702	autosomal dominant epidermolytic ichthyosis
MONDO:0019723	disease of glomerular basement membrane
MONDO:0020701	brachydactyly type A1A
MONDO:0020700	microcephaly, short stature, and impaired glucose metabolism
MONDO:0019726	type II mixed cryoglobulinemia
MONDO:0019725	pediatric systemic lupus erythematosus
MONDO:0019720	non-syndromic renal or urinary tract malformation
MONDO:0032721	spondyloepiphyseal dysplasia, kondo-fu type
MONDO:0019722	glomerular disease
MONDO:0019721	syndromic renal or urinary tract malformation
MONDO:0020709	Majocchi granuloma
MONDO:0020708	brachial amyotrophic diplegia
MONDO:0020707	central hearing loss
MONDO:0007728	acne inversa, familial, 1
MONDO:0032728	Charcot-Marie-Tooth disease, axonal, type 2EE
MONDO:0007729	developmental dysplasia of the hip 1
MONDO:0032729	intellectual developmental disorder, autosomal recessive 70
MONDO:0032726	combined oxidative phosphorylation deficiency 39
MONDO:0007726	hip dysplasia, Beukes type
MONDO:0007727	autosomal dominant familial periodic fever
MONDO:0007724	hirsutism-skeletal dysplasia-intellectual disability syndrome
MONDO:0032724	spondyloepimetaphyseal dysplasia with joint laxity, type 3
MONDO:0007725	hereditary progressive mucinous histiocytosis
MONDO:0032725	developmental and epileptic encephalopathy, 74
MONDO:0007722	heterochromia iridis
MONDO:0007723	Hirschsprung disease, susceptibility to, 1
MONDO:0032723	immunodeficiency 60
MONDO:0007720	hernia, double inguinal
MONDO:0007721	hiatus hernia
MONDO:0044710	lip and oral cavity squamous cell carcinoma
MONDO:0019709	cleidocranial dysplasia and isolated cranial ossification defect
MONDO:0019717	chromosomal disease with overgrowth
MONDO:0019716	overgrowth syndrome
MONDO:0044705	paranasal sinus squamous cell carcinoma
MONDO:0019719	congenital anomaly of kidney and urinary tract
MONDO:0019718	lethal chondrodysplasia
MONDO:0019713	non-syndromic limb reduction defect
MONDO:0044702	X-linked external auditory canal atresia-dilated internal auditory canal-facial dysmorphism syndrome
MONDO:0019712	patellar dysostosis
MONDO:0044701	childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder
MONDO:0019715	syndrome with synostosis or other joint formation defect
MONDO:0044704	oropharynx squamous cell carcinoma
MONDO:0019714	non-syndromic polydactyly, syndactyly and/or hyperphalangy
MONDO:0032732	deafness, autosomal recessive 113
MONDO:0019711	dysostosis with predominant vertebral and costal involvement
MONDO:0032730	leukodystrophy, hypomyelinating, 18
MONDO:0019710	dysostosis with predominant craniofacial involvement
MONDO:0044709	cochleovestibular dysplasia
MONDO:0007719	diaphragmatic hernia, congenital 1
MONDO:0032739	spermatogenic failure 36
MONDO:0007739	Huntington disease
MONDO:0007737	humeroradial synostosis
MONDO:0032737	spastic paraplegia 80, autosomal dominant
MONDO:0007738	spondyloepiphyseal dysplasia with congenital joint dislocations
MONDO:0032738	gonadal dysgenesis, dysmorphic facies, retinal dystrophy, and myopathy
MONDO:0007735	congenital Horner syndrome
MONDO:0032735	cataract 48
MONDO:0007736	HPA 1 Recognition polymorphism, beta-globin-related
MONDO:0032736	metabolic crises, recurrent, with variable encephalomyopathic features and neurologic regression
MONDO:0007733	holoprosencephaly 3
MONDO:0032733	global developmental delay, progressive ataxia, and elevated glutamine
MONDO:0007734	holoprosencephaly 4
MONDO:0007731	HLA modifier
MONDO:0044720	cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome
MONDO:0007732	Holt-Oram syndrome
MONDO:0044721	severe combined immunodeficiency due to LAT deficiency
MONDO:0007730	histiocytic dermatoarthritis
MONDO:0019706	lysosomal storage disease with skeletal involvement
MONDO:0044717	4q25 proximal deletion syndrome
MONDO:0019705	primary bone dysplasia with defective bone mineralization
MONDO:0044716	STAG1-related intellectual disability-facial dysmorphism-gastroesophageal reflux syndrome
MONDO:0019708	primary bone dysplasia with disorganized development of skeletal components
MONDO:0044719	erythema multiforme major
MONDO:0019707	primary osteolysis
MONDO:0044718	alkaline ceramidase 3 deficiency
MONDO:0019702	neonatal osteosclerotic dysplasia
MONDO:0019701	chondrodysplasia punctata
MONDO:0019704	primary bone dysplasia with decreased bone density
MONDO:0044715	metopic ridging-ptosis-facial dysmorphism syndrome
MONDO:0019703	primary bone dysplasia with increased bone density
MONDO:0044714	mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome
MONDO:0032742	encephalopathy, acute, infection-induced, susceptibility to, 9
MONDO:0032740	deafness, autosomal recessive 100
MONDO:0019700	primary bone dysplasia with multiple joint dislocations
MONDO:0032741	neurodevelopmental disorder with impaired speech and hyperkinetic movements
MONDO:0005127	lepromatous leprosy
MONDO:0005126	tuberculoid leprosy
MONDO:0005129	cataract
MONDO:0007788	hypertriglyceridemia, familial
MONDO:0007789	hypertrophia musculorum vera
MONDO:0005128	sensory system disease
MONDO:0020764	Brown-Pearce carcinoma
MONDO:0005123	Hibiscus chlorotic ringspot virus infection
MONDO:0007786	hypertrichosis lanuginosa congenita
MONDO:0007787	Ambras type hypertrichosis universalis congenita
MONDO:0005122	Pectobacterium carotovorum infection
MONDO:0020763	Menke-Hennekam syndrome 1
MONDO:0005125	borderline leprosy
MONDO:0020762	diencephalic-mesencephalic junction dysplasia syndrome 2
MONDO:0007784	selective pituitary resistance to thyroid hormone
MONDO:0020761	Bowen disease of the skin
MONDO:0005124	leprosy
MONDO:0007785	hyperthyroxinemia, dystransthyretinemic
MONDO:0020760	skin squamous cell carcinoma in situ
MONDO:0007782	hyperthermia, cutaneous, with headaches and nausea
MONDO:0007783	malignant hyperthermia, susceptibility to, 1
MONDO:0005121	Enterococcus faecalis infection
MONDO:0007780	hypertelorism, Teebi type
MONDO:0007781	essential hypertension, genetic
MONDO:0005120	Drosophila C virus infection
MONDO:0020759	epilepsy, childhood absence, susceptibility to, 1
MONDO:0020757	sporadic hemiplegic migraine
MONDO:0019779	Renier-Gabreels-Jasper syndrome
MONDO:0017116	congenital communicating hydrocephalus
MONDO:0020756	migraine, familial hemiplegic, 1
MONDO:0019778	Smith-Fineman-Myers syndrome
MONDO:0017117	congenital non-communicating hydrocephalus
MONDO:0020755	heart block
MONDO:0017118	syndrome with a cerebellar malformation as major feature
MONDO:0020754	visceral myopathy
MONDO:0017119	syndrome with microcephaly as major feature
MONDO:0019775	Chudley-Lowry-Hoar syndrome
MONDO:0017112	isolated unilateral hemispheric cerebellar hypoplasia
MONDO:0019774	Holmes-Gang syndrome
MONDO:0017113	isolated bilateral hemispheric cerebellar hypoplasia
MONDO:0019777	Carpenter-Waziri syndrome
MONDO:0017114	global cerebellar malformation
MONDO:0019776	Juberg-Marsidi syndrome
MONDO:0017115	bifid nose
MONDO:0019771	oromandibular dystonia
MONDO:0019770	X-linked dominant intellectual disability-epilepsy syndrome
MONDO:0019773	myelomeningocele
MONDO:0017110	isolated Dandy-Walker malformation with hydrocephalus
MONDO:0019772	blepharospasm-oromandibular dystonia syndrome
MONDO:0017111	isolated Dandy-Walker malformation without hydrocephalus
MONDO:0005138	lung carcinoma
MONDO:0005137	nutritional disorder
MONDO:0007799	hypophosphatemic bone disease
MONDO:0005139	morbid obesity
MONDO:0007797	hypoparathyroidism-deafness-renal disease syndrome
MONDO:0020753	Orthocoronavirinae infectious disease
MONDO:0005134	experimental autoimmune encephalomyelitis
MONDO:0005133	endometriosis
MONDO:0020752	EJM1
MONDO:0007798	adult hypophosphatasia
MONDO:0005136	malaria
MONDO:0007795	mullerian duct anomalies-limb anomalies syndrome
MONDO:0020751	orthostatic hypotension 2
MONDO:0005135	parasitic infectious disease
MONDO:0007796	hypoparathyroidism, familial isolated 1
MONDO:0020750	polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 2
MONDO:0005130	celiac disease
MONDO:0007793	hypochondroplasia
MONDO:0007794	hypogonadotropic hypogonadism 7 with or without anosmia
MONDO:0005132	cytomegalovirus infection
MONDO:0007791	familial hypocalciuric hypercalcemia 1
MONDO:0007792	familial hypocalciuric hypercalcemia 2
MONDO:0005131	cervical carcinoma
MONDO:0017109	isolated partial cerebellar vermis agenesis
MONDO:0007790	Charcot-Marie-Tooth disease type 3
MONDO:0020749	polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 1
MONDO:0020748	sitosterolemia 2
MONDO:0020747	sitosterolemia 1
MONDO:0019768	X-linked intellectual disability, Golabi-Ito-hall type
MONDO:0020746	contractures, pterygia, and variable skeletal fusions syndrome 1B
MONDO:0017105	glioependymal/ependymal cyst
MONDO:0017106	retrocerebellar cyst
MONDO:0019767	hamel cerebro-palato-cardiac syndrome
MONDO:0020745	autosomal dominant cardiac arrhythmia (Kuhn)
MONDO:0020744	Mobitz type I atrioventricular block
MONDO:0017107	isolated cerebellar vermis agenesis
MONDO:0020743	mixed phenotype acute leukemia
MONDO:0019769	X-linked intellectual disability, Sutherland-Haan type
MONDO:0017108	isolated total cerebellar vermis agenesis
MONDO:0017101	isolated focal cortical dysplasia type IIa
MONDO:0019764	laryngotracheoesophageal cleft type 4
MONDO:0017102	isolated focal cortical dysplasia type IIb
MONDO:0019763	laryngotracheoesophageal cleft type 3
MONDO:0019766	X-linked intellectual disability, Porteous type
MONDO:0017103	encephaloclastic disorder
MONDO:0019765	Celosomia
MONDO:0017104	central nervous system cystic malformation
MONDO:0019760	terminal transverse defects of arm
MONDO:0019762	laryngotracheoesophageal cleft type 2
MONDO:0017100	neutropenia-monocytopenia-deafness syndrome
MONDO:0019761	laryngotracheoesophageal cleft type 1
MONDO:0005109	HIV infectious disease
MONDO:0005108	viral infectious disease
MONDO:0007768	hyperparathyroidism 2 with jaw tumors
MONDO:0005105	melanoma
MONDO:0007769	hyperpigmentation of eyelid
MONDO:0005104	aJCC grade 1 sarcoma
MONDO:0007766	Morgagni-Stewart-Morel syndrome
MONDO:0005107	hepatocellular adenoma
MONDO:0005106	lipoma
MONDO:0007767	hyperparathyroidism 1
MONDO:0005101	ulcerative colitis
MONDO:0007764	autosomal dominant osteosclerosis, Worth type
MONDO:0020742	cataract, microcephaly, failure to thrive, kyphoscoliosis syndrome
MONDO:0005100	systemic sclerosis
MONDO:0007765	hyperostosis cranialis interna
MONDO:0020741	pyridoxine-dependent epilepsy caused by ALDH7A1 mutant
MONDO:0005103	well-differentiated liposarcoma
MONDO:0007762	hyperlipoproteinemia type V
MONDO:0020740	ectodermal dysplasia and immunodeficiency 1
MONDO:0005102	undifferentiated (embryonal) sarcoma
MONDO:0007763	nonpapillary renal cell carcinoma
MONDO:0007760	hyperlipoproteinemia, type II, and deafness
MONDO:0007761	hyperlipoproteinemia type IV
MONDO:0020739	autosomal recessive infantile hypercalcemia 1
MONDO:0020738	multiple benign circumferential skin creases on limbs 1
MONDO:0020737	optic atrophy 10 with or without ataxia, intellectual disability, and seizures
MONDO:0020736	uncombable hair syndrome 1
MONDO:0020735	ACTH-independent macronodular adrenal hyperplasia 1
MONDO:0019757	alobar holoprosencephaly
MONDO:0020734	erythrocyte AMP deaminase deficiency
MONDO:0019756	lobar holoprosencephaly
MONDO:0019759	epispadias
MONDO:0020733	proximal symphalangism 1A
MONDO:0019758	midline interhemispheric variant of holoprosencephaly
MONDO:0020732	progeria
MONDO:0019753	localized Castleman disease
MONDO:0019752	pediatric Castleman disease
MONDO:0019755	developmental defect during embryogenesis
MONDO:0019754	multicentric Castleman disease
MONDO:0019751	autoinflammatory syndrome
MONDO:0019750	rare renal disease
MONDO:0005119	anthrax infection
MONDO:0005116	Whipple disease
MONDO:0007779	autosomal dominant Opitz G/BBB syndrome
MONDO:0005115	temporal lobe epilepsy
MONDO:0005118	human granulocytic ehrlichiosis
MONDO:0007777	hypertaurinuric cardiomyopathy
MONDO:0007778	hypertelorism
MONDO:0005117	Aeromonas hydrophila infectious disease
MONDO:0020731	arbovirus infection
MONDO:0007775	hypersecretion of adrenal androgens, familial
MONDO:0005112	malignant pleural mesothelioma
MONDO:0005111	Epstein-Barr virus infection
MONDO:0007776	hypersensitivity pneumonitis, familial
MONDO:0020730	carpal tunnel syndrome 1
MONDO:0005114	pneumococcal infection
MONDO:0007773	hyperproglucagonemia
MONDO:0007774	hyperreflexia
MONDO:0005113	bacterial infectious disease
MONDO:0007771	hyperpigmentation with or without hypopigmentation, familial progressive
MONDO:0007772	pseudohypoaldosteronism type 2A
MONDO:0005110	idiopathic cardiomyopathy
MONDO:0007770	hyperpigmentation of Fuldauer and Kuijpers
MONDO:0020728	hypouricemia, renal 1
MONDO:0019749	rare renal tumor
MONDO:0020727	combined oxidative phosphorylation deficiency 22
MONDO:0020726	tubulointerstitial kidney disease, autosomal dominant, 2
MONDO:0020725	anemia due to chronic disorder
MONDO:0020724	cerebral cavernous malformation 1
MONDO:0019746	cystinuria type B
MONDO:0020723	vitamin D-dependent rickets, type 1A
MONDO:0019745	cystinuria type A
MONDO:0019748	rare cause of hypertension
MONDO:0020722	nephrolithiasis susceptibility caused by SLC26A1
MONDO:0019747	hematological disorder with renal involvement
MONDO:0020721	X-linked sideroblastic anemia 1
MONDO:0019742	late-onset nephronophthisis
MONDO:0019741	familial cystic renal disease
MONDO:0019744	rare renal tubular disease
MONDO:0019743	nephropathy secondary to a storage or other metabolic disease
MONDO:0019740	acquired thrombotic thrombocytopenic purpura
MONDO:0020729	autosomal recessive agammaglobulinemia 1
MONDO:0007706	cavernous hemangiomas of face-supraumbilical midline raphe syndrome
MONDO:0007707	hemangiomas of small intestine
MONDO:0007704	osteoarthritis susceptibility 2
MONDO:0007705	Heinz body anemia
MONDO:0007702	heart-hand syndrome type 3
MONDO:0007703	heart, malformation of
MONDO:0007700	hawkinsinuria
MONDO:0007701	progressive familial heart block type II
MONDO:0007717	hemoglobin--variants for which the chain carrying the mutation 1S unknown or uncertain
MONDO:0007718	hepatic adenomas, familial
MONDO:0007715	hemolytic poikilocytic anemia due to reduced ankyrin binding sites
MONDO:0007716	alpha thalassemia-intellectual disability syndrome type 1
MONDO:0007713	clonic hemifacial spasm
MONDO:0007714	migraine, familial hemiplegic, 1
MONDO:0007711	Bencze syndrome
MONDO:0007712	oculoauriculovertebral spectrum with radial defects
MONDO:0007710	facial hemiatrophy
MONDO:0007708	Kasabach-Merritt syndrome
MONDO:0007709	hematuria, benign familial
MONDO:0032591	hyperparathyroidism, transient neonatal
MONDO:0032592	cardiomyopathy, dilated, 2c
MONDO:0032590	ovarian dysgenesis 8
MONDO:0032599	immunodeficiency 15a
MONDO:0032597	myasthenic syndrome, congenital, 24, presynaptic
MONDO:0032598	developmental and epileptic encephalopathy, 68
MONDO:0032596	myasthenic syndrome, congenital, 23, presynaptic
MONDO:0032594	intellectual developmental disorder and retinitis pigmentosa; IDDRP
MONDO:0019571	autosomal dominant cutis laxa
MONDO:0019570	Cockayne syndrome type 2
MONDO:0007588	extrasystoles-short stature-hyperpigmentation-microcephaly syndrome
MONDO:0020566	Klatskin tumor
MONDO:0007589	exudative vitreoretinopathy 1
MONDO:0020565	adenocarcinoma of esophagus
MONDO:0007586	exostoses, multiple, type 2
MONDO:0020564	well-differentiated liposarcoma
MONDO:0020563	Dedifferentiated liposarcoma
MONDO:0007587	external auditory canal atresia-vertical talus-hypertelorism syndrome
MONDO:0020562	pleomorphic liposarcoma
MONDO:0007584	exostoses-anetodermia-brachydactyly type E syndrome
MONDO:0020561	myxoid/round cell liposarcoma
MONDO:0007585	exostoses, multiple, type 1
MONDO:0020560	atypical teratoid rhabdoid tumor
MONDO:0007582	Cockayne syndrome B
MONDO:0007583	exostoses of heel
MONDO:0007580	esterase ES-2, regulator for
MONDO:0007581	exchondrosis of pinna, posterior
MONDO:0020559	O'Sullivan-McLeod syndrome
MONDO:0020558	autosomal dominant Charcot-Marie-Tooth disease type 2K
MONDO:0020557	pleuropulmonary blastoma type 3
MONDO:0020556	pleuropulmonary blastoma type 2
MONDO:0019577	anonychia-onychodystrophy syndrome
MONDO:0019576	telangiectasia macularis eruptiva perstans
MONDO:0019579	discrete papular lichen myxedematosus
MONDO:0019578	nodular lichen myxedematosus
MONDO:0019573	autosomal recessive cutis laxa type 2
MONDO:0019572	autosomal recessive cutis laxa type 1
MONDO:0019575	hypotrichosis simplex of the scalp
MONDO:0019574	secondary intestinal lymphangiectasia
MONDO:0019560	lupus erythematosus tumidus
MONDO:0007599	factor 9 and Factor XI, combined deficiency of
MONDO:0020555	pleuropulmonary blastoma type 1
MONDO:0020554	Heiner syndrome
MONDO:0007597	factor VIII and Factor IX, combined deficiency of
MONDO:0020553	secondary pulmonary hemosiderosis
MONDO:0020552	placental site trophoblastic tumor
MONDO:0007598	factors VIII, IX and XI, combined deficiency of
MONDO:0020551	hydatidiform mole
MONDO:0007595	factor VII and Factor VIII, combined deficiency of
MONDO:0020550	gestational choriocarcinoma
MONDO:0007596	factor VIII deficiency
MONDO:0007593	facial spasm
MONDO:0007594	factor 5 excess with spontaneous thrombosis
MONDO:0007591	facial hypertrichosis
MONDO:0007592	familial recurrent peripheral facial palsy
MONDO:0020549	invasive hydatidiform mole
MONDO:0007590	hemifacial hypertrophy
MONDO:0020548	ocular pemphigoid
MONDO:0019569	Cockayne syndrome type 1
MONDO:0020547	chronic graft versus host disease
MONDO:0020546	acute graft versus host disease
MONDO:0020545	staphylococcal toxic-shock syndrome
MONDO:0032566	squalene synthase deficiency
MONDO:0019566	Klippel-Trenaunay syndrome
MONDO:0019565	hereditary von Willebrand disease
MONDO:0032567	isolated growth hormone deficiency, type 4
MONDO:0019568	Ehlers-Danlos syndrome, classic type, 2
MONDO:0032564	hennekam lymphangiectasia-lymphedema syndrome 3
MONDO:0019567	Ehlers-Danlos syndrome, classic type, 1
MONDO:0032565	ophthalmoplegia, external, with rib and vertebral anomalies
MONDO:0019562	localized scleroderma
MONDO:0019561	lupus erythematosus panniculitis
MONDO:0019564	systemic sclerosis
MONDO:0019563	CREST syndrome
MONDO:0007568	aortic aneurysm, familial thoracic 4
MONDO:0032568	intellectual developmental disorder with macrocephaly, seizures, and speech delay
MONDO:0007569	erythema nodosum, familial
MONDO:0032569	isolated growth hormone deficiency, type 5
MONDO:0007566	multiple self-healing squamous epithelioma
MONDO:0020544	streptococcal toxic-shock syndrome
MONDO:0007567	Epstein-Barr virus insertion site 1
MONDO:0020543	theca steroid-producing cell malignant tumor of ovary, not further specified
MONDO:0020542	malignant Sertoli-Leydig cell tumor of ovary
MONDO:0007564	pilomatrixoma
MONDO:0020541	maligant granulosa cell tumor of ovary
MONDO:0007565	familial cylindromatosis
MONDO:0007562	multiple epiphyseal dysplasia, Beighton type
MONDO:0020540	ovarian gynandroblastoma
MONDO:0007563	epistaxis, hereditary
MONDO:0007560	reading seizures
MONDO:0007561	multiple epiphyseal dysplasia type 1
MONDO:0032570	Joubert syndrome 35
MONDO:0020539	extragonadal non-dysgerminomatous germ cell tumor
MONDO:0020538	malignant dysgerminomatous germ cell tumor of ovary
MONDO:0020537	occupational allergic alveolitis
MONDO:0019559	hypertrophic or verrucous lupus erythematosus
MONDO:0019558	discoid lupus erythematosus
MONDO:0020536	pigeon-breeder lung disease
MONDO:0020535	house allergic alveolitis
MONDO:0020534	farmer's lung
MONDO:0032577	retinitis pigmentosa 83
MONDO:0019555	panniculitis and localized lipodystrophy
MONDO:0032578	cortical dysplasia, complex, with other brain malformations 9
MONDO:0019554	idiopathic localized lipodystrophy
MONDO:0019557	chilblain lupus
MONDO:0032575	diarrhea 9
MONDO:0019556	pressure-induced localized lipoatrophy
MONDO:0032573	bone marrow failure syndrome 5
MONDO:0019551	hereditary motor and sensory neuropathy type 6
MONDO:0019550	hereditary motor and sensory neuropathy with acrodystrophy
MONDO:0032574	osteochondrodysplasia, brachydactyly, and overlapping malformed digits
MONDO:0019553	drug-induced localized lipodystrophy
MONDO:0032571	spondyloepimetaphyseal dysplasia, Krakow type
MONDO:0032572	cardiac, facial, and digital anomalies with developmental delay
MONDO:0019552	centrifugal lipodystrophy
MONDO:0007579	esterase C
MONDO:0032579	warburg-cinotti syndrome
MONDO:0007577	esophageal ring, lower
MONDO:0020533	streptobacillary rat-bite fever
MONDO:0007578	esterase B
MONDO:0020532	spirillary rat-bite fever
MONDO:0020531	long chain acyl-CoA dehydrogenase deficiency
MONDO:0007575	erythrokeratodermia variabilis
MONDO:0020530	mendelian susceptibility to mycobacterial diseases due to complete IFNgammaR1 deficiency
MONDO:0007576	esophageal cancer
MONDO:0007573	acute erythroleukemia, familial
MONDO:0007574	spinocerebellar ataxia type 34
MONDO:0007571	primary erythermalgia
MONDO:0007572	primary familial polycythemia due to EPO receptor mutation
MONDO:0032580	nephrotic syndrome, type 17
MONDO:0007570	erythema palmare hereditarium
MONDO:0020529	ACTH-independent Cushing syndrome
MONDO:0032581	nephrotic syndrome, type 18
MONDO:0020528	ACTH-dependent Cushing syndrome
MONDO:0020527	ectopic Cushing syndrome
MONDO:0019548	autosomal dominant intermediate Charcot-Marie-Tooth disease
MONDO:0020526	acute megakaryoblastic leukemia in down syndrome
MONDO:0019547	Wells syndrome
MONDO:0020525	transient neonatal diabetes mellitus
MONDO:0020524	primary parathyroid hyperplasia
MONDO:0019549	severe early-onset axonal neuropathy due to MFN2 deficiency
MONDO:0020523	familial parathyroid adenoma
MONDO:0019544	cocaine intoxication
MONDO:0032588	periventricular nodular heterotopia 8
MONDO:0019543	acquired aneurysmal subarachnoid hemorrhage
MONDO:0032586	diarrhea 10, protein-losing enteropathy type
MONDO:0019546	other acquired skin disease
MONDO:0019545	systemic monochloroacetate poisoning
MONDO:0019540	diffuse alveolar hemorrhage
MONDO:0032584	ectodermal dysplasia 14, hair/tooth type with or without hypohidrosis
MONDO:0019542	acute liver failure
MONDO:0032582	nephrotic syndrome, type 19
MONDO:0019541	non-infectious posterior uveitis
MONDO:0032583	microcephaly 24, primary, autosomal recessive
MONDO:0020591	disease of peritoneum
MONDO:0020590	mycobacterial infectious disease
MONDO:0020599	acquired coagulation factor deficiency
MONDO:0020598	malabsorption syndrome
MONDO:0020597	angiokeratoma of scrotum
MONDO:0020596	mucin-producing carcinoma
MONDO:0020595	disease of retroperitoneum
MONDO:0020594	abducens nerve disease
MONDO:0020593	trichoblastoma
MONDO:0020592	disease of pharynx
MONDO:0020589	cardiac germ cell tumor
MONDO:0020580	germinomatous germ cell tumor
MONDO:0019591	panhypopituitarism
MONDO:0019590	rare endocrine growth disease
MONDO:0019593	46,XX disorder of sex development induced by fetal androgens excess
MONDO:0019592	disorder of sex development
MONDO:0032526	spinocerebellar ataxia 48
MONDO:0020588	lung PEComa
MONDO:0020587	factor XI deficiency
MONDO:0020586	factor V deficiency
MONDO:0020585	anemia due to erythrocyte enzyme disorder
MONDO:0020584	anemia due to enzyme disorder
MONDO:0020583	chromosome 17 abnormality
MONDO:0020582	benign uterine ligament neoplasm
MONDO:0020581	benign PEComa
MONDO:0020579	mucositis
MONDO:0020578	vitamin D deficiency
MONDO:0019599	primary lipodystrophy
MONDO:0019598	fragile X syndrome
MONDO:0019595	46,XY disorder of sex development due to adrenal and testicular steroidogenesis defect
MONDO:0019594	46,XY disorder of sex development due to a testosterone synthesis defect
MONDO:0019597	46,XY disorder of sex development due to isolated 17,20-lyase deficiency
MONDO:0019596	46,XY disorder of sex development due to testicular steroidogenesis defect
MONDO:0019580	papular mucinosis of infancy
MONDO:0019582	self-healing papular mucinosis
MONDO:0019581	acral persistent papular mucinosis
MONDO:0020577	childhood gonadal germ cell tumor
MONDO:0020576	cutaneous vasculitis
MONDO:0020575	polymorphic ventricular tachycardia
MONDO:0020574	central nervous system nongerminomatous germ cell tumor
MONDO:0020573	inherited disease susceptibility
MONDO:0020572	complex regional pain syndrome type 2
MONDO:0020571	relapsing epidemic typhus
MONDO:0020570	Brill-Zinsser disease
MONDO:0020569	intermediate DEND syndrome
MONDO:0020568	cutaneous myiasis
MONDO:0020567	apnea of prematurity
MONDO:0019588	deafness, autosomal recessive
MONDO:0019587	autosomal dominant nonsyndromic deafness
MONDO:0019589	syndromic genetic deafness
MONDO:0019584	localized lichen myxedematosus with monoclonal gammopathy or systemic symptoms
MONDO:0019583	localized lichen myxedematosus with mixed features of different subtypes
MONDO:0019586	X-linked nonsyndromic deafness
MONDO:0019585	scleromyxedema without monoclonal gammopathy
MONDO:0007629	fragile site 10Q23
MONDO:0007627	focal facial dermal dysplasia type I
MONDO:0007628	foveal hypoplasia 1
MONDO:0007625	focal epithelial hyperplasia of the oral mucosa
MONDO:0007626	familial congenital palsy of trochlear nerve
MONDO:0007623	flushing of ears and somnolence
MONDO:0007624	Flynn-Aird syndrome
MONDO:0007621	floating-Harbor syndrome
MONDO:0007622	flood factor deficiency
MONDO:0007620	fish eye disease
MONDO:0019618	Sheehan syndrome
MONDO:0019617	pituitary deficiency due to empty sella turcica syndrome
MONDO:0019619	duplication of the esophagus
MONDO:0019614	pituitary deficiency due to Rathke's pouch cysts
MONDO:0019613	non-functioning pituitary adenoma
MONDO:0019616	germinoma of the central nervous system
MONDO:0019615	pituitary dermoid and epidermoid cysts
MONDO:0019610	Zollinger-Ellison syndrome
MONDO:0019612	functioning gonadotropic adenoma
MONDO:0019611	TSH-secreting pituitary adenoma
MONDO:0007638	fucosidase regulator
MONDO:0007639	fundus albipunctatus
MONDO:0007636	frontorhiny
MONDO:0007637	corneal dystrophy, Fuchs endothelial, 1
MONDO:0007634	intellectual disability, FRA12A type
MONDO:0007635	Frasier syndrome
MONDO:0007632	fragile site, Distamycin a type, rare, fra(16)(q22.1)
MONDO:0007633	Friedreich ataxia, so-called, with optic atrophy and sensorineural deafness
MONDO:0007630	North Carolina macular dystrophy
MONDO:0007631	chromosome 16p12.1 deletion syndrome, 520kb
MONDO:0019607	unspecified juvenile idiopathic arthritis
MONDO:0019606	simple cryoglobulinemia
MONDO:0019609	Zellweger spectrum disorders
MONDO:0019608	46,XX disorder of sex development induced by maternal-derived androgen
MONDO:0019603	osteopenia-myopia-hearing loss-intellectual disability-facial dysmorphism syndrome
MONDO:0019602	other inborn metabolic disease
MONDO:0019605	immunotactoid or fibrillary glomerulopathy
MONDO:0019604	acquired monoclonal Ig light chain-associated Fanconi syndrome
MONDO:0032600	Snijders Blok-Campeau syndrome
MONDO:0019601	autosomal recessive axonal hereditary motor and sensory neuropathy
MONDO:0019600	xeroderma pigmentosum
MONDO:0007607	Birt-Hogg-Dube syndrome
MONDO:0032607	vertebral anomalies and variable endocrine and T-cell dysfunction
MONDO:0007608	desmoid tumor
MONDO:0032608	mitochondrial complex 1 deficiency, nuclear type 3
MONDO:0007605	fibrinolytic defect
MONDO:0032605	intellectual disability, autosomal recessive 66
MONDO:0007606	fibrodysplasia ossificans progressiva
MONDO:0032606	mitochondrial complex 1 deficiency, nuclear type 2
MONDO:0007603	Felty syndrome
MONDO:0032603	polydactyly, postaxial, type A9
MONDO:0032604	retinitis pigmentosa 84
MONDO:0007604	femoral-facial syndrome
MONDO:0007601	familial Mediterranean fever, autosomal dominant
MONDO:0032601	inflammatory bowel disease, immunodeficiency, and encephalopathy
MONDO:0007602	favism, susceptibility to
MONDO:0007600	primary Fanconi syndrome
MONDO:0032609	mitochondrial complex 1 deficiency, nuclear type 4
MONDO:0032610	mitochondrial complex 1 deficiency, nuclear type 5
MONDO:0032611	mitochondrial complex 1 deficiency, nuclear type 6
MONDO:0007618	Eng-Strom syndrome
MONDO:0032618	mitochondrial complex 1 deficiency, nuclear type 13
MONDO:0007619	isolated congenital adermatoglyphia
MONDO:0032619	mitochondrial complex 1 deficiency, nuclear type 14
MONDO:0032616	mitochondrial complex 1 deficiency, nuclear type 10
MONDO:0007616	fibula, recurrent dislocation of head of
MONDO:0007617	Coffin-Siris syndrome 1
MONDO:0032617	mitochondrial complex 1 deficiency, nuclear type 11
MONDO:0007614	congenital fibrosis of extraocular muscles
MONDO:0032614	epidermodysplasia verruciformis, susceptibility to, 2
MONDO:0032615	mitochondrial complex 1 deficiency, nuclear type 9
MONDO:0007615	laurin-Sandrow syndrome
MONDO:0007612	gingival fibromatosis-progressive deafness syndrome
MONDO:0032612	mitochondrial complex 1 deficiency, nuclear type 7
MONDO:0032613	mitochondrial complex 1 deficiency, nuclear type 8
MONDO:0007613	fibromuscular dysplasia of arteries
MONDO:0007610	gingival fibromatosis-hypertrichosis syndrome
MONDO:0007611	Zimmermann-Laband syndrome
MONDO:0032621	mitochondrial complex 1 deficiency, nuclear type 16
MONDO:0032622	mitochondrial complex 1 deficiency, nuclear type 17
MONDO:0032620	mitochondrial complex 1 deficiency, nuclear type 15
MONDO:0007609	fibromatosis, gingival, 1
MONDO:0005009	congestive heart failure
MONDO:0005006	clear cell sarcoma of kidney
MONDO:0007669	renal cysts and diabetes syndrome
MONDO:0005005	clear cell renal carcinoma
MONDO:0007667	subependymoma
MONDO:0005008	colorectal adenocarcinoma
MONDO:0005007	colon mucinous adenocarcinoma
MONDO:0007668	globulin anomaly involving beta (2A)-globulin
MONDO:0020643	autism susceptibility 1
MONDO:0007665	glaucoma 1, open angle, E
MONDO:0005002	chronic obstructive pulmonary disease
MONDO:0005001	chronic gastritis
MONDO:0007666	glaucoma-sleep apnea syndrome
MONDO:0020642	polycystic kidney disease
MONDO:0005004	clear cell adenocarcinoma
MONDO:0007663	glaucoma with elevated episcleral venous pressure
MONDO:0020641	respiratory tract neoplasm
MONDO:0007664	glaucoma 1, open angle, A
MONDO:0005003	chronic pancreatitis
MONDO:0020640	autoimmune encephalitis
MONDO:0007661	Tourette syndrome
MONDO:0007662	anterior segment dysgenesis 4
MONDO:0005000	chromophobe renal cell carcinoma
MONDO:0007660	familial ossifying fibroma
MONDO:0020639	monosomy
MONDO:0020638	superficial spreading melanoma
MONDO:0020637	mendelian susceptibility to mycobacterial diseases due to a partial deficiency
MONDO:0020636	mendelian susceptibility to mycobacterial diseases due to a complete deficiency
MONDO:0019658	sporadic idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial proliferation
MONDO:0020635	anaplastic meningioma
MONDO:0019657	sporadic idiopathic steroid-resistant nephrotic syndrome with minimal changes
MONDO:0020634	grade III meningioma
MONDO:0020633	anaplastic cancer
MONDO:0019659	Pfeiffer syndrome type 1
MONDO:0019654	familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis
MONDO:0019653	familial idiopathic steroid-resistant nephrotic syndrome with minimal changes
MONDO:0019656	sporadic idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis
MONDO:0019655	sporadic idiopathic steroid-resistant nephrotic syndrome with focal segmental hyalinosis
MONDO:0019650	idiopathic steroid-sensitive nephrotic syndrome with minimal change
MONDO:0019652	familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial proliferation
MONDO:0019651	idiopathic steroid-sensitive nephrotic syndrome with diffuse mesangial proliferation
MONDO:0005017	diffuse gastric adenocarcinoma
MONDO:0005016	diabetic kidney disease
MONDO:0005019	diffuse scleroderma
MONDO:0007678	glycoprotein, renal
MONDO:0007679	GMS syndrome
MONDO:0005018	diffuse large B-cell lymphoma
MONDO:0007676	glutathione transferase activity toward trans-stilbene oxide
MONDO:0005013	dedifferentiated chondrosarcoma
MONDO:0020632	epileptic encephalopathy, infantile or early childhood, 3
MONDO:0005012	cutaneous melanoma
MONDO:0020631	epileptic encephalopathy, infantile or early childhood, 2
MONDO:0007677	hyperglycinuria
MONDO:0020630	epileptic encephalopathy, infantile or early childhood, 1
MONDO:0005015	diabetes mellitus
MONDO:0007674	glucose-6-phosphate dehydrogenase-like
MONDO:0007675	glutamic acid decarboxylase, brain, membrane form
MONDO:0005014	dermatomyositis
MONDO:0007672	glomuvenous malformation
MONDO:0007673	Glucoglycinuria
MONDO:0005011	Crohn disease
MONDO:0007670	hypotrichosis-lymphedema-telangiectasia syndrome (grouping)
MONDO:0005010	coronary artery disease
MONDO:0007671	fibronectin glomerulopathy
MONDO:0020629	microcephaly, growth restriction and increased sister chromatid exchange
MONDO:0020628	microcephaly, growth restriction, and increased sister chromatid exchange 2
MONDO:0020627	epileptic encephalopathy, infantile or early childhood
MONDO:0020626	yt blood group antigen
MONDO:0019647	congenital bilateral megacalycosis
MONDO:0020625	blood group--wright antigen
MONDO:0020624	blood group--waldner type
MONDO:0019646	unilateral congenital megacalycosis
MONDO:0019649	idiopathic steroid-sensitive nephrotic syndrome with focal segmental hyalinosis
MONDO:0020623	blood group--ul system
MONDO:0019648	achondrogenesis
MONDO:0020622	blood group--stoltzfus system
MONDO:0019643	transient pseudohypoaldosteronism
MONDO:0019642	vitamin D-dependent rickets, type 2
MONDO:0019645	renal dysplasia, bilateral
MONDO:0019644	renal dysplasia, unilateral
MONDO:0019641	pauci-immune glomerulonephritis
MONDO:0019640	posterior urethral valve
MONDO:0007649	gastric juice peptides
MONDO:0007647	gastric volvulus, intrathoracic
MONDO:0007648	hereditary diffuse gastric adenocarcinoma
MONDO:0007645	gastric sneezing
MONDO:0007646	Gamstorp-Wohlfart syndrome
MONDO:0007643	gamma-A-globulin, defect in assembly of
MONDO:0020621	blood group--scianna system
MONDO:0007644	IgAD1
MONDO:0020620	blood group, ss
MONDO:0007641	Futcher line
MONDO:0007642	isolated agenesis of gallbladder
MONDO:0007640	Sorsby fundus dystrophy
MONDO:0020618	blood group--private systems
MONDO:0019639	congenital megacalycosis
MONDO:0020617	blood group--ok
MONDO:0020616	blood group, mn
MONDO:0020615	blood group system, landsteiner-wiener
MONDO:0020614	blood group--lutheran system
MONDO:0019636	renal agenesis, unilateral
MONDO:0019635	idiopathic achalasia
MONDO:0020613	blood group--lke
MONDO:0020612	blood group, kidd system
MONDO:0019638	renal dysplasia
MONDO:0019637	renal hypoplasia
MONDO:0020611	blood group--kell system
MONDO:0019632	Lyme disease
MONDO:0019631	persistent hyperplastic primary vitreous
MONDO:0019634	familial nasal acilia
MONDO:0019633	relapsing fever
MONDO:0019630	congenital ectropion uveae
MONDO:0020619	blood group, langereis system
MONDO:0007658	spitz nevus
MONDO:0007659	giant platelet syndrome with thrombocytopenia
MONDO:0007656	Gerstmann-Straussler-Scheinker syndrome
MONDO:0007657	giant neutrophil leukocytes
MONDO:0007654	genu valgum, st. Helena familial
MONDO:0020610	blood group, diego system
MONDO:0007655	fissured tongue
MONDO:0007652	gastric mucosal hypertrophy
MONDO:0007653	genochondromatosis
MONDO:0007650	MALT lymphoma
MONDO:0007651	gastrocutaneous syndrome
MONDO:0019629	sclerocornea
MONDO:0020607	Liddle syndrome 1
MONDO:0020606	sex-linked disease
MONDO:0019628	Rieger anomaly
MONDO:0020605	X-linked recessive disease
MONDO:0020604	X-linked dominant disease
MONDO:0019625	familial thoracic aortic aneurysm and aortic dissection
MONDO:0020603	X-linked chondrodysplasia punctata 2
MONDO:0019624	acquired angioedema
MONDO:0020602	Simpson-Golabi-Behmel syndrome type 1
MONDO:0019627	isolated congenital alacrima
MONDO:0020601	mosquito-borne viral encephalitis
MONDO:0019626	isolated ankyloblepharon filiforme adnatum
MONDO:0020600	acute pharyngitis
MONDO:0019621	chronic pneumonitis of infancy
MONDO:0019620	congenital esophageal diverticulum
MONDO:0019623	hereditary angioedema
MONDO:0019622	non-specific interstitial pneumonia
MONDO:0020609	blood group, colton system
MONDO:0020608	blood group--ahonen
MONDO:0020492	hemimegalencephaly
MONDO:0020491	subcortical band heterotopia
MONDO:0020490	mosaic trisomy 9
MONDO:0020499	Nipah virus disease
MONDO:0020498	Lassa fever
MONDO:0020497	Turcot syndrome with polyposis
MONDO:0020496	familial porencephaly
MONDO:0020495	peho-like syndrome
MONDO:0020494	oculootodental syndrome
MONDO:0020493	Haddad syndrome
MONDO:0032485	intellectual developmental disorder 61
MONDO:0019450	lissencephaly with cerebellar hypoplasia
MONDO:0007469	double nail for fifth toe
MONDO:0020445	agenesis of the superior vena cava
MONDO:0007467	DNA, low-repetitive sequences of
MONDO:0020444	subaortic course of innominate vein
MONDO:0007468	DNA, satellite, alpha type
MONDO:0020443	absence of innominate vein
MONDO:0007465	distichiasis with congenital anomalies of the heart and peripheral vasculature
MONDO:0020442	left superior vena cava persisting to left-sided atrium
MONDO:0007466	DNA, satellite, 3
MONDO:0020441	right superior vena cava connecting to left-sided atrium
MONDO:0007463	distal osteosclerosis
MONDO:0007464	isolated distichiasis
MONDO:0020440	persistent left superior vena cava connecting to the left-sided atrium
MONDO:0007461	short stature-valvular heart disease-characteristic facies syndrome
MONDO:0007462	multiple sclerosis, susceptibility to
MONDO:0007460	discrimination, Two-point, reduction 1N
MONDO:0020439	patent foramen ovale
MONDO:0020438	atrial septal aneurysm
MONDO:0020437	atrial septal defect, ostium primum type
MONDO:0019459	myeloid sarcoma
MONDO:0020436	atrial septal defect, sinus venosus type
MONDO:0044406	arthrogryposis-ectodermal dysplasia-other anomalies syndrome
MONDO:0020435	atrial septal defect, coronary sinus type
MONDO:0019456	acute myeloid leukemia with multilineage dysplasia
MONDO:0019455	acute panmyelosis with myelofibrosis
MONDO:0019458	acute basophilic leukemia
MONDO:0019457	therapy related acute myeloid leukemia and myelodysplastic syndrome
MONDO:0019452	myeloproliferative neoplasm, unclassifiable
MONDO:0019451	chronic neutrophilic leukemia
MONDO:0019454	myelodysplastic syndrome with excess blasts
MONDO:0019453	refractory cytopenia with multilineage dysplasia
MONDO:0020434	atrial septal defect, ostium secundum type
MONDO:0007478	autosomal dominant Kenny-Caffey syndrome
MONDO:0007479	dwarfism, Levi type
MONDO:0020433	ectasia of the left appendage
MONDO:0007476	familial Dupuytren contracture
MONDO:0020432	ectasia of the right atrial appendage
MONDO:0020431	juxtaposition of the atrial appendages
MONDO:0007477	3-M syndrome
MONDO:0007474	duodenal ulcer due to antral G-cell hyperfunction
MONDO:0020430	cor triatriatum sinister
MONDO:0007475	duodenal ulcer, hyperpepsinogenemic 1
MONDO:0007472	basal laminar drusen
MONDO:0007473	Duane retraction syndrome
MONDO:0007470	calvarial doughnut lesions-bone fragility syndrome
MONDO:0007471	Doyne honeycomb retinal dystrophy
MONDO:0020429	cor triatriatum dexter
MONDO:0020428	congenital Gerbode defect
MONDO:0019449	lissencephaly type 3-familial fetal akinesia sequence syndrome
MONDO:0020427	Laubry-Pezzi syndrome
MONDO:0019448	benign adult familial myoclonic epilepsy
MONDO:0020426	malposition of the coronary ostium
MONDO:0020425	abnormal number of coronary ostia
MONDO:0020424	intramural coronary arterial course
MONDO:0019445	trichofolliculoma
MONDO:0019444	Trichinellosis
MONDO:0019447	atypical lichen myxedematosus
MONDO:0019446	localized lichen myxedematosus
MONDO:0019441	ATTRV122I amyloidosis
MONDO:0019440	wild type ABeta2M amyloidosis
MONDO:0019443	dextro-looped transposition of the great arteries
MONDO:0019442	congenital toxoplasmosis
MONDO:0007449	dermo-odonto dysplasia
MONDO:0007447	autosomal dominant vibratory urticaria
MONDO:0007448	familial dermatographia
MONDO:0007445	dermatopathia pigmentosa reticularis
MONDO:0020423	stenosis or atrophy of the coronary ostium
MONDO:0007446	dermatosis papulosa nigra
MONDO:0020422	aortopulmonary coronary arterial course
MONDO:0020421	coronary artery intramyocardial course
MONDO:0007443	congenital unilateral hypoplasia of depressor anguli oris
MONDO:0007444	dermal Ridges, patternless
MONDO:0020420	pulmonary branch stenosis
MONDO:0007441	dentinogenesis imperfecta type 2
MONDO:0007442	dentinogenesis imperfecta type 3
MONDO:0007440	major affective disorder 1
MONDO:0020419	pulmonary artery hypoplasia
MONDO:0020418	dysphagia lusoria
MONDO:0020417	right aortic arch
MONDO:0019438	AL amyloidosis
MONDO:0020416	Neuhauser anomaly
MONDO:0019437	enthesitis-related juvenile idiopathic arthritis
MONDO:0020415	Kommerell diverticulum
MONDO:0020414	persistent fifth aortic arch
MONDO:0019439	AA amyloidosis
MONDO:0020413	encircling double aortic arch
MONDO:0019434	systemic-onset juvenile idiopathic arthritis
MONDO:0019433	oligoarticular juvenile idiopathic arthritis
MONDO:0019436	psoriasis-related juvenile idiopathic arthritis
MONDO:0019435	rheumatoid factor-positive polyarticular juvenile idiopathic arthritis
MONDO:0019430	X-linked intellectual disability-ataxia-apraxia syndrome
MONDO:0019432	rheumatoid factor-negative juvenile idiopathic arthritis
MONDO:0019431	primitive portal vein thrombosis
MONDO:0007458	digitotalar dysmorphism; ulnar drift, hereditary
MONDO:0007459	dilution, pigmentary
MONDO:0020412	congenital patent ductus arteriosus aneurysm
MONDO:0007456	diarrhea, glucose-stimulated secretory, with common variable immunodeficiency
MONDO:0007457	diastema, dental medial
MONDO:0020411	aorto-left ventricular tunnel
MONDO:0007454	type 1 diabetes mellitus 2
MONDO:0020410	aorto-right ventricular tunnel
MONDO:0007455	diabetes mellitus, noninsulin-dependent
MONDO:0007452	maturity-onset diabetes of the young type 1
MONDO:0007453	maturity-onset diabetes of the young type 2
MONDO:0007450	neurohypophyseal diabetes insipidus
MONDO:0007451	diabetes insipidus, nephrogenic, autosomal
MONDO:0020409	univentricular heart with single atrio-ventricular valve
MONDO:0020408	complete atrioventricular canal-tetralogy of fallot syndrome
MONDO:0020407	complete atrioventricular canal-ventricle hypoplasia syndrome
MONDO:0020406	complete atrioventricular canal-left heart obstruction syndrome
MONDO:0019427	X-linked neurodegenerative syndrome, Bertini type
MONDO:0020405	straddling and/or overriding mitral valve
MONDO:0019426	X-linked intellectual disability-corpus callosum agenesis-spastic quadriparesis syndrome
MONDO:0020404	shone complex
MONDO:0019429	X-linked neurodegenerative syndrome, Hamel type
MONDO:0020403	congenital mitral valve agenesis
MONDO:0020402	congenital accessory mitral valve tissue
MONDO:0019428	fried syndrome
MONDO:0019423	X-linked intellectual disability, Stoll type
MONDO:0019422	X-linked intellectual disability, Stevenson type
MONDO:0019425	X-linked intellectual disability-hypotonia-facial dysmorphism-aggressive behavior syndrome
MONDO:0019424	X-linked intellectual disability-acromegaly-hyperactivity syndrome
MONDO:0019421	X-linked intellectual disability, Seemanova type
MONDO:0019420	X-linked intellectual disability, Pai type
MONDO:0020481	myotonia fluctuans
MONDO:0019492	desmoid tumor
MONDO:0019491	rare intellectual disability
MONDO:0020480	sulfite oxidase deficiency due to molybdenum cofactor deficiency
MONDO:0019494	primary pediatric heart tumor
MONDO:0019493	primary adult heart tumor
MONDO:0019490	progressive familial heart block
MONDO:0020489	familial hyperreninemic hypoaldosteronism type 1
MONDO:0020488	atypical progressive supranuclear palsy syndrome
MONDO:0020487	Pontiac fever
MONDO:0020485	King-Denborough syndrome
MONDO:0020484	rare familial disorder with hypertrophic cardiomyopathy
MONDO:0020483	acetazolamide-responsive myotonia
MONDO:0020482	myotonia permanens
MONDO:0020479	pituitary gigantism
MONDO:0019499	Turner syndrome
MONDO:0019496	neuroendocrine neoplasm
MONDO:0019495	yolk sac tumor
MONDO:0019498	tungiasis
MONDO:0019497	nonsyndromic genetic deafness
MONDO:0020470	49,XYYYY syndrome
MONDO:0019481	follicular dendritic cell sarcoma
MONDO:0019480	Langerhans cell sarcoma
MONDO:0019483	methotrexate-associated lymphoproliferative disorders
MONDO:0019482	dendritic cell sarcoma not otherwise specified
MONDO:0020478	Leber plus disease
MONDO:0020477	progeria-associated arthropathy
MONDO:0020476	mesial temporal lobe epilepsy with hippocampal sclerosis
MONDO:0020475	dermotrichic syndrome
MONDO:0020474	cheirospondyloenchondromatosis
MONDO:0020473	dappled diaphyseal dysplasia
MONDO:0020472	Turner syndrome due to structural X chromosome anomalies
MONDO:0020471	pituitary adenoma
MONDO:0020469	48,XYYY syndrome
MONDO:0020468	paternal uniparental disomy of chromosome 13
MONDO:0019489	diffuse palmoplantar keratoderma - acrocyanosis syndrome
MONDO:0019488	myoclonic epilepsy in non-progressive encephalopathies
MONDO:0019485	idiopathic hemiconvulsion-hemiplegia syndrome
MONDO:0019484	hypothalamic hamartomas with gelastic seizures
MONDO:0019487	epilepsy with myoclonic absences
MONDO:0019486	myoclonic epilepsy of infancy
MONDO:0019470	aggressive NK-cell leukemia
MONDO:0019472	extranodal nasal NK/T cell lymphoma
MONDO:0019471	adult T-cell leukemia/lymphoma
MONDO:0007489	dysplasia epiphysealis hemimelica
MONDO:0020467	mosaic monosomy X
MONDO:0020466	monosomy X
MONDO:0007487	dyslexia, susceptibility to, 1
MONDO:0020465	congenital eyelid retraction
MONDO:0020464	euryblepharon
MONDO:0007488	Lewy body dementia
MONDO:0007485	dyskeratosis congenita, autosomal dominant 1
MONDO:0020463	isolated congenital ectropion
MONDO:0020462	tarsal kink syndrome
MONDO:0007486	hereditary benign intraepithelial dyskeratosis
MONDO:0007483	dyschromatosis symmetrica hereditaria
MONDO:0020461	epiblepharon
MONDO:0007484	dyschromatosis universalis
MONDO:0020460	acquired von willebrand syndrome
MONDO:0007481	Leri-Weill dyschondrosteosis
MONDO:0007482	dyschondrosteosis-nephritis syndrome
MONDO:0007480	dwarfism with stiff joints and ocular abnormalities
MONDO:0020459	unstable hemoglobin disease
MONDO:0020458	hemolytic anemia due to erythrocyte adenosine deaminase overproduction
MONDO:0020457	6-phosphogluconate dehydrogenase deficiency
MONDO:0019478	adult nodular lymphocyte predominant Hodgkin lymphoma
MONDO:0019477	angioimmunoblastic T-cell lymphoma
MONDO:0019479	histiocytic sarcoma
MONDO:0019474	hepatosplenic T-cell lymphoma
MONDO:0019473	enteropathy-associated T-cell lymphoma
MONDO:0019476	primary cutaneous peripheral T-cell lymphoma not otherwise specified
MONDO:0019475	subcutaneous panniculitis-like T-cell lymphoma
MONDO:0019461	B-cell prolymphocytic leukemia
MONDO:0019460	acute leukemia of ambiguous lineage
MONDO:0020456	pleuro-pericardial cyst
MONDO:0020455	congenital partial agenesis of pericardium
MONDO:0020454	congenital complete agenesis of pericardium
MONDO:0007498	ear exostoses
MONDO:0020453	congenital partial pulmonary venous return anomaly
MONDO:0007499	ear folding
MONDO:0020452	inferior vena cava interruption
MONDO:0007496	dystonia 12
MONDO:0007497	ear antitragus, tag at base of
MONDO:0020451	congenital stenosis of the inferior vena cava
MONDO:0007494	episodic kinesigenic dyskinesia 1
MONDO:0020450	azygos continuation of the inferior vena cava
MONDO:0007495	dystonia 5
MONDO:0007492	early-onset generalized limb-onset dystonia
MONDO:0007493	torsion dystonia 4
MONDO:0007490	carpotarsal osteochondromatosis
MONDO:0007491	dystelephalangy
MONDO:0020449	persistent eustachian valve
MONDO:0020448	right inferior vena cava connecting to left-sided atrium
MONDO:0020447	coronary sinus atresia
MONDO:0020446	coronary sinus stenosis
MONDO:0019467	CD4+/CD56+ hematodermic neoplasm
MONDO:0019466	lymphomatoid granulomatosis
MONDO:0019469	T-cell large granular lymphocyte leukemia
MONDO:0019468	T-cell prolymphocytic leukemia
MONDO:0019463	non-amyloid monoclonal immunoglobulin deposition disease
MONDO:0019462	splenic marginal zone lymphoma
MONDO:0019465	nodal marginal zone B-cell lymphoma
MONDO:0019464	heavy chain disease
MONDO:0007508	Rapp-Hodgkin syndrome
MONDO:0007509	ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominant
MONDO:0007506	obsoleted echo virus 11 sensitivity
MONDO:0007507	absence of fingerprints-congenital milia syndrome
MONDO:0007504	thickened earlobes-conductive deafness syndrome
MONDO:0007505	earring holes, natural
MONDO:0007502	ear pits, posterior helical
MONDO:0007503	ear without helix
MONDO:0007500	ear malformation
MONDO:0007501	preauricular fistulae, congenital
MONDO:0007519	Edinburgh malformation syndrome
MONDO:0007517	ectrodactyly-cleft palate syndrome
MONDO:0007518	edema, familial idiopathic, prepubertal
MONDO:0007515	ectopia pupillae
MONDO:0007516	ectrodactyly and ectodermal dysplasia without cleft lip/palate
MONDO:0007513	ectodermal dysplasia with adrenal cyst
MONDO:0007514	ectopia lentis 1, isolated, autosomal dominant
MONDO:0007511	ectodermal dysplasia, trichoodontoonychial type
MONDO:0007512	ectodermal dysplasia syndrome with distinctive facial appearance and preaxial polydactyly of feet
MONDO:0007510	Clouston syndrome
MONDO:0007548	transient bullous dermolysis of the newborn
MONDO:0007549	generalized dominant dystrophic epidermolysis bullosa
MONDO:0007546	myeloproliferative disorder, chronic, with eosinophilia
MONDO:0007547	epidermoid cysts
MONDO:0020522	Ehlers-Danlos syndrome type 7B
MONDO:0007544	eosinophilia, familial
MONDO:0020521	Ehlers-Danlos syndrome type 7A
MONDO:0007545	Eosinophilopenia
MONDO:0020520	adult pulmonary Langerhans cell histiocytosis
MONDO:0007542	Camurati-Engelmann disease
MONDO:0007543	enolase, sperm specific
MONDO:0007540	multiple endocrine neoplasia type 1
MONDO:0007541	endometriosis, susceptibility to, 1
MONDO:0020519	hand-Schuller-Christian disease
MONDO:0020518	Hashimoto-Pritzker syndrome
MONDO:0020517	eosinophilic granuloma
MONDO:0020516	thymic neuroendocrine carcinoma
MONDO:0019537	hemoglobin D disease
MONDO:0020515	thymic carcinoma
MONDO:0019536	typical hemolytic-uremic syndrome
MONDO:0020514	thymoma
MONDO:0020513	spermatocytic seminoma
MONDO:0019539	retinopathy of prematurity
MONDO:0019538	Gaisbock syndrome
MONDO:0020512	precursor T-cell acute lymphoblastic leukemia
MONDO:0019533	paroxysmal cold hemoglobinuria
MONDO:0019532	autoimmune hemolytic anemia, warm type
MONDO:0019535	drug-induced autoimmune hemolytic anemia
MONDO:0019534	mixed-type autoimmune hemolytic anemia
MONDO:0019531	hemolytic anemia due to glutathione reductase deficiency
MONDO:0019530	non-syndromic syndactyly
MONDO:0007559	photoparoxysmal response 1
MONDO:0007557	epidermolysis bullosa with congenital localized absence of skin and deformity of nails
MONDO:0007558	benign occipital epilepsy
MONDO:0007555	epidermolysis bullosa simplex Ogna type
MONDO:0020511	precursor B-cell acute lymphoblastic leukemia
MONDO:0007556	epidermolysis bullosa simplex with mottled pigmentation
MONDO:0020510	idiopathic syringomyelia
MONDO:0007553	epidermolysis bullosa with deficiency of galactosylhydroxylysyl glucosyltransferase
MONDO:0007554	generalized epidermolysis bullosa simplex, non-Dowling-Meara type
MONDO:0007551	localized epidermolysis bullosa simplex
MONDO:0007552	pretibial dystrophic epidermolysis bullosa
MONDO:0007550	epidermolysis bullosa simplex Dowling-Meara type
MONDO:0020508	primary syringomyelia
MONDO:0019529	radiation myelitis
MONDO:0020507	Cree leukoencephalopathy
MONDO:0020506	ovarioleukodystrophy
MONDO:0020505	ravine syndrome
MONDO:0019526	erythema elevatum diutinum
MONDO:0020504	genetic recurrent myoglobinuria
MONDO:0019525	tetrasomy X
MONDO:0020503	resistance to thyrotropin-releasing hormone syndrome
MONDO:0020502	yellow fever
MONDO:0019528	IgG4-related hepatopathy
MONDO:0019527	undifferentiated connective tissue syndrome
MONDO:0020501	Crimean-Congo hemorrhagic fever
MONDO:0019522	recessive dystrophic epidermolysis bullosa-generalized other
MONDO:0019521	centripetalis recessive dystrophic epidermolysis bullosa
MONDO:0019524	infantile Bartter syndrome with sensorineural deafness
MONDO:0019523	Walker-Warburg syndrome
MONDO:0019520	syndromic lymphedema
MONDO:0020509	secondary syringomyelia
MONDO:0007528	Ehlers-Danlos syndrome, autosomal dominant, type unspecified
MONDO:0007529	elastosis perforans serpiginosa
MONDO:0007526	Ehlers-Danlos syndrome progeroid type
MONDO:0007527	Ehlers-Danlos syndrome, periodontitis type
MONDO:0007524	autosomal dominant Ehlers-Danlos syndrome, vascular type
MONDO:0007525	Ehlers-Danlos syndrome, arthrochalasis type
MONDO:0020500	Marburg hemorrhagic fever
MONDO:0007522	Ehlers-Danlos syndrome, classic type
MONDO:0007523	Ehlers-Danlos syndrome, hypermobility type
MONDO:0007520	ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 1
MONDO:0007521	egasyn
MONDO:0019519	rare skin disease
MONDO:0019518	Waardenburg-Shah syndrome
MONDO:0019515	rare dementia
MONDO:0019514	hepatic veno-occlusive disease
MONDO:0019517	Waardenburg syndrome type 2
MONDO:0019516	exudative vitreoretinopathy
MONDO:0019511	autosomal dominant medullary cystic kidney disease with hyperuricemia
MONDO:0019510	autosomal dominant medullary cystic kidney disease without hyperuricemia
MONDO:0019513	esophageal malformation
MONDO:0019512	congenital heart malformation
MONDO:0007539	encephalopathy, recurrent, of childhood
MONDO:0007537	lateral meningocele syndrome
MONDO:0007538	amelogenesis imperfecta, type 3A
MONDO:0007535	emphysema, hereditary pulmonary
MONDO:0007536	congenital lobar emphysema
MONDO:0007533	elliptocytosis 2
MONDO:0007534	Beckwith-Wiedemann syndrome
MONDO:0007531	electroencephalographic peculiarity: fronto-precentral beta wave groups
MONDO:0007532	Electroencephalographic peculiarity: occipital slow beta waves
MONDO:0007530	electroencephalographic peculiarity: 14 and 6 per sec. positive spike phenomenon
MONDO:0019508	van der Woude syndrome
MONDO:0019507	amelogenesis imperfecta
MONDO:0019509	cutaneous leukocytoclastic angiitis
MONDO:0019504	superior limbic keratoconjunctivitis
MONDO:0019503	anterior segment dysgenesis
MONDO:0019506	obesity-colitis-hypothyroidism-cardiac hypertrophy-developmental delay syndrome
MONDO:0019505	hypomyelination-hypogonadotropic hypogonadism-hypodontia syndrome
MONDO:0019500	extragonadal teratoma
MONDO:0019502	autosomal recessive non-syndromic intellectual disability
MONDO:0019501	Usher syndrome
MONDO:0020393	discrete fibromuscular subaortic stenosis
MONDO:0020392	discrete fixed membranous subaortic stenosis
MONDO:0020391	pulmonary artery coming from the aorta
MONDO:0020390	pulmonary artery coming from patent ductus arteriosus
MONDO:0020399	congenital hypoplasia of the mitral valve annulus
MONDO:0020398	congenital mitral stenosis
MONDO:0020397	parachute tricuspid valve
MONDO:0020396	anomaly of the tricuspid valve chordae
MONDO:0020395	valvar pulmonary stenosis
MONDO:0020394	tunnel subaortic stenosis
MONDO:0020382	multifocal pattern dystrophy simulating fundus flavimaculatus
MONDO:0019393	idiopathic malabsorption due to bile acid synthesis defects
MONDO:0020381	patterned macular dystrophy
MONDO:0019392	syringocystadenoma papilliferum
MONDO:0020380	autosomal dominant cerebellar ataxia
MONDO:0019395	Hinman syndrome
MONDO:0019394	Senior-Boichis syndrome
MONDO:0019391	Fanconi anemia
MONDO:0019390	Susac syndrome
MONDO:0020389	pulmonary valve agenesis-ventricular septal defect-persistent ductus arteriosus syndrome
MONDO:0020388	double outlet right ventricle with non-committed subpulmonary ventricular septal defect
MONDO:0020387	double outlet right ventricle with subpulmonary ventricular septal defect
MONDO:0020386	double outlet right ventricle with subaortic or doubly committed ventricular septal defect with pulmonary stenosis
MONDO:0020385	congenitally uncorrected transposition of the great arteries with coarctation
MONDO:0020384	Niemann-Pick disease type E
MONDO:0020383	fundus pulverulentus
MONDO:0400006	botryomycosis
MONDO:0400004	phrynoderma
MONDO:0400005	refeeding syndrome
MONDO:0400002	calcium-alkali syndrome
MONDO:0400003	skeletal fluorosis
MONDO:0400000	small intestinal bacterial overgrowth
MONDO:0019397	unknown leukodystrophy
MONDO:0019396	collagen type III glomerulopathy
MONDO:0019399	Isaac syndrome
MONDO:0019398	desmin-related myopathy with Mallory body-like inclusions
MONDO:0019382	Colorado tick fever
MONDO:0020371	essential iris atrophy
MONDO:0020370	Cogan-Reese syndrome
MONDO:0019381	eastern equine encephalitis
MONDO:0019384	encephalitis lethargica
MONDO:0019383	acute disseminated encephalomyelitis
MONDO:0019380	western equine encephalitis
MONDO:0020379	early-onset zonular cataract
MONDO:0020378	early-onset posterior polar cataract
MONDO:0020377	early-onset partial cataract
MONDO:0020376	early-onset nuclear cataract
MONDO:0020375	coralliform cataract
MONDO:0020374	cerulean cataract
MONDO:0020373	early-onset anterior polar cataract
MONDO:0020372	early-onset sutural cataract
MONDO:0020369	Chandler syndrome
MONDO:0019389	X-linked recessive intellectual disability-macrocephaly-ciliary dysfunction syndrome
MONDO:0019386	progressive rubella panencephalitis
MONDO:0019385	steroid-responsive encephalopathy associated with autoimmune thyroiditis
MONDO:0019388	pelvis syndrome
MONDO:0019387	macrostomia-preauricular tags-external ophthalmoplegia syndrome
MONDO:0044335	benign soft tissue neoplasm
MONDO:0044334	connective and soft tissue neoplasm
MONDO:0044337	stromal sarcoma
MONDO:0044336	colorectal signet ring cell carcinoma
MONDO:0044331	genetic transient congenital hypothyroidism
MONDO:0044330	hyperekplexia 4
MONDO:0044333	alcohol-induced Wernicke-Korsakoff's syndrome
MONDO:0044332	childhood-onset benign chorea with striatal involvement
MONDO:0044328	short-rib thoracic dysplasia 20 with polydactyly
MONDO:0044327	polycystic liver disease 4 with or without kidney cysts
MONDO:0044329	osteogenesis imperfecta, type 18
MONDO:0044346	echinococcus granulosus infectious disease
MONDO:0044345	Schistosoma mansoni infectious disease
MONDO:0044348	hemoglobinopathy
MONDO:0044347	erythrocyte disease
MONDO:0044342	thoracic disc degenerative disorder
MONDO:0044344	Schistosoma japonicum infectious disease
MONDO:0044343	cervical disc degenerative disorder
MONDO:0044339	lumbar disc degenerative disorder
MONDO:0044338	autoimmune primary ovarian failure
MONDO:0044351	Schistosoma intercalatum infectious disease
MONDO:0044350	hyperparathyroidism, primary, caused by water clear cell hyperplasia
MONDO:0044355	isolated sternocostoclavicular hyperostosis
MONDO:0044354	Rosai-Dorfman disease
MONDO:0044349	acquired hemoglobinopathy
MONDO:0022981	die Smulders droog van dijk syndrome
MONDO:0022982	die Smulders Vles Fryns syndrome
MONDO:0022983	Dieterich disease
MONDO:0007348	colchicine resistance
MONDO:0022985	diffuse cavernous hemangioma of the rectum
MONDO:0022986	diffuse idiopathic pulmonary neuroendocrine cell hyperplasia
MONDO:0007349	familial cold autoinflammatory syndrome 1
MONDO:0007346	cochleosaccular degeneration-cataract syndrome
MONDO:0010998	ALG3-CDG
MONDO:0020324	intravascular large B-cell lymphoma
MONDO:0020323	primary mediastinal large B-cell lymphoma
MONDO:0010997	supranuclear palsy, progressive, 1
MONDO:0007347	Coxsackievirus B3 susceptibility
MONDO:0020322	acute biphenotypic leukemia
MONDO:0007344	cluster headache, familial
MONDO:0020321	acute undifferentiated leukemia
MONDO:0010999	fallot complex-intellectual disability-growth delay syndrome
MONDO:0007345	aorta coarctation
MONDO:0020320	acute myeloblastic leukemia with maturation
MONDO:0007342	clubfoot
MONDO:0007343	isolated congenital digital clubbing
MONDO:0007340	cleidocranial dysplasia
MONDO:0007341	cleidorhizomelic syndrome
MONDO:0020319	acute myeloblastic leukemia without maturation
MONDO:0019339	47,XYY syndrome
MONDO:0020317	acute myeloid leukemia with 11q23 abnormalities
MONDO:0019338	sarcoidosis
MONDO:0020316	acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22)
MONDO:0020315	unclassified myelodysplastic syndrome
MONDO:0020314	refractory anemia
MONDO:0019335	mild hyperphenylalaninemia
MONDO:0034976	iatrogenic Creutzfeldt-Jakob disease
MONDO:0022977	diaphragmatic hernia exomphalos corpus callosum agenesis
MONDO:0019334	autosomal recessive hyperinsulinism due to Kir6.2 deficiency
MONDO:0022978	diaphragmatic hernia upper limb defects
MONDO:0019337	autoimmune bullous skin disease
MONDO:0019336	Gardner syndrome
MONDO:0019331	rare form of salmonellosis
MONDO:0019330	pili gemini
MONDO:0019333	autosomal recessive hyperinsulinism due to SUR1 deficiency
MONDO:0019332	punctate palmoplantar keratoderma type 1
MONDO:0022971	diabetes persistent mullerian ducts
MONDO:0022972	diabetic mastopathy
MONDO:0007359	commissural lip pits
MONDO:0022975	diaphragmatic agenesis radial aplasia omphalocele
MONDO:0044302	congenital heart defects, dysmorphic facial features, and intellectual developmental disorder
MONDO:0007357	colonic varices without portal hypertension
MONDO:0020313	unclassified myelodysplastic/myeloproliferative disease
MONDO:0010987	autosomal recessive nonsyndromic deafness 8
MONDO:0007358	comedones, familial Dyskeratotic
MONDO:0010986	autosomal recessive nonsyndromic deafness 9
MONDO:0044301	aortic aneurysm, familial thoracic 11, susceptibility to
MONDO:0020312	atypical chronic myeloid leukemia
MONDO:0020311	chronic myelomonocytic leukemia
MONDO:0007355	uveal coloboma-cleft lip and palate-intellectual disability
MONDO:0044304	hyperphenylalaninemia due to DNAJC12 deficiency
MONDO:0010989	Mayer-Rokitansky-Küster-Hauser syndrome type 2
MONDO:0010988	aplasia cutis-myopia syndrome
MONDO:0007356	Lynch syndrome 1
MONDO:0044303	congenital heart defects and ectodermal dysplasia
MONDO:0020310	familial focal epilepsy with variable foci
MONDO:0007353	coloboma of macula-brachydactyly type B syndrome
MONDO:0007354	coloboma of optic nerve
MONDO:0044300	familial adenomatous polyposis 4
MONDO:0007351	coloboma of macula
MONDO:0007352	renal coloboma syndrome
MONDO:0010990	Cd4/CD8 T-cell ratio
MONDO:0007350	coloboma, ocular, autosomal dominant
MONDO:0020309	Landau-Kleffner syndrome
MONDO:0010992	Ayme-Gripp syndrome
MONDO:0020308	benign childhood occipital epilepsy, Gastaut type
MONDO:0020307	benign childhood occipital epilepsy, Panayiotopoulos type
MONDO:0010991	laterality defects, autosomal dominant
MONDO:0020306	absent tibia-polydactyly syndrome
MONDO:0010994	micromelic dwarfism, Fryns type
MONDO:0019328	macrocystic lymphatic malformation
MONDO:0010993	Harrod syndrome
MONDO:0019327	phakomatosis spilorosea
MONDO:0020305	isochromosomy Yq
MONDO:0010996	hereditary hemorrhagic telangiectasia type 3
MONDO:0020304	isochromosomy Yp
MONDO:0010995	Charcot-Marie-Tooth disease type 1C
MONDO:0020303	Angelman syndrome due to paternal uniparental disomy of chromosome 15
MONDO:0019329	microcystic lymphatic malformation
MONDO:0022965	desmoplastic infantile ganglioglioma
MONDO:0019324	pemphigus foliaceus
MONDO:0034987	intraductal tubulopapillary neoplasm of pancreas
MONDO:0019323	pemphigus erythematosus
MONDO:0019326	phakomatosis cesiomarmorata
MONDO:0019325	phakomatosis cesioflammea
MONDO:0022968	dextrocardia with situs inversus
MONDO:0019320	acanthokeratolytic verrucous nevus
MONDO:0019322	pemphigus vegetans
MONDO:0019321	atypical Werner syndrome
MONDO:0022960	dermatocardioskeletal syndrome boronne type
MONDO:0007328	choroidal osteoma, bilateral
MONDO:0007329	cirrhosis, familial
MONDO:0022963	desmoplastic infantile astrocytoma
MONDO:0007326	paroxysmal nonkinesigenic dyskinesia 1
MONDO:0009989	enhanced S-cone syndrome
MONDO:0007327	chylomicronemia, familial, due to circulating inhibitor of lipoprotein lipase
MONDO:0009988	retinoschisis of fovea
MONDO:0009987	autosomal recessive pericentral pigmentary retinopathy
MONDO:0044313	intellectual disability, autosomal recessive 60
MONDO:0010976	KRT14-related epidermolysis bullosa simplex
MONDO:0020302	Angelman syndrome due to maternal 15q11q13 deletion
MONDO:0007324	chorea
MONDO:0010975	arrhythmogenic right ventricular dysplasia 2
MONDO:0044312	immunoskeletal dysplasia with neurodevelopmental abnormalities
MONDO:0007325	choreoathetosis, familial inverted
MONDO:0009986	retinopathy, pigmentary, and intellectual disability
MONDO:0020301	Prader-Willi syndrome due to paternal 15q11q13 deletion
MONDO:0007322	chondrodysplasia punctata, tibial-metacarpal type
MONDO:0010978	portal vein, cavernous transformation of
MONDO:0044315	craniosynostosis 7
MONDO:0020300	autosomal dominant nocturnal frontal lobe epilepsy
MONDO:0009985	retinohepatoendocrinologic syndrome
MONDO:0044314	retinitis pigmentosa 78
MONDO:0010977	Brody myopathy
MONDO:0007323	Chondronectin
MONDO:0009984	late-adult onset retinitis pigmentosa
MONDO:0009983	retinitis pigmentosa-intellectual disability-deafness-hypogenitalism syndrome
MONDO:0007320	chondrocalcinosis due to apatite crystal deposition
MONDO:0007321	autosomal dominant chondrodysplasia punctata
MONDO:0010979	Timothy syndrome
MONDO:0009982	retinitis pigmentosa inversa with deafness
MONDO:0044311	brachycephaly, trichomegaly, and developmental delay
MONDO:0009981	retinitis pigmentosa type 1
MONDO:0044310	Diamond-Blackfan anemia 17
MONDO:0009980	retinal telangiectasia and hypogammaglobulinemia
MONDO:0044309	Diamond-Blackfan anemia 16
MONDO:0010981	absent tibia-polydactyly-arachnoid cyst syndrome
MONDO:0010980	midline malformations, multiple, with limb abnormalities and hypopituitarism
MONDO:0010983	dystonia 9
MONDO:0044306	neurodevelopmental disorder with epilepsy, cataracts, feeding difficulties, and delayed brain myelination
MONDO:0019317	follicular atrophoderma-basal cell carcinoma
MONDO:0019316	maculopapular cutaneous mastocytosis
MONDO:0010982	ichthyosis-intellectual disability syndrome with large keratohyalin granules in the skin
MONDO:0044305	ectodermal dysplasia 13, hair/tooth type
MONDO:0019319	verrucous nevus
MONDO:0010985	epilepsy, familial adult myoclonic, 1
MONDO:0044308	bardet-biedl syndrome 21
MONDO:0010984	Usher syndrome type 1D
MONDO:0019318	inflammatory linear verrucous epidermal nevus
MONDO:0019313	lymphatic malformation
MONDO:0019312	Hermansky-Pudlak syndrome
MONDO:0019315	diffuse cutaneous mastocytosis
MONDO:0019314	cutaneous mastocytoma
MONDO:0019311	woolly hair nevus
MONDO:0019310	recessive dystrophic epidermolysis bullosa inversa
MONDO:0007339	blepharocheilodontic syndrome
MONDO:0007337	cleft palate-lateral synechia syndrome
MONDO:0022953	delta-1-pyrroline-5-carboxylate dehydrogenase deficiency
MONDO:0007338	cleft soft palate
MONDO:0009999	autosomal recessive Robinow syndrome
MONDO:0044324	Al Kaissi syndrome
MONDO:0009998	Richieri Costa-Pereira syndrome
MONDO:0010965	autosomal recessive nonsyndromic deafness 6
MONDO:0007335	orofacial cleft 1
MONDO:0009997	Roberts syndrome
MONDO:0044323	Rahman syndrome
MONDO:0007336	isolated cleft palate
MONDO:0010964	epiphyseal dysplasia, multiple, 3
MONDO:0044326	developmental delay and seizures with or without movement abnormalities
MONDO:0009996	rhizomelic syndrome, Urbach type
MONDO:0007333	van der Woude syndrome 1
MONDO:0010967	autosomal recessive nonsyndromic deafness 7
MONDO:0009995	rheumatic fever-related antigen
MONDO:0007334	autosomal dominant popliteal pterygium syndrome
MONDO:0010966	achondrogenesis type IB
MONDO:0044325	Fanconi anemia, complementation group W
MONDO:0009994	alveolar rhabdomyosarcoma
MONDO:0010969	cone-rod dystrophy 5
MONDO:0007331	cleft chin
MONDO:0044320	retinitis pigmentosa 79
MONDO:0009993	embryonal rhabdomyosarcoma
MONDO:0007332	split-hand/foot malformation with long bone deficiency 1
MONDO:0010968	glaucoma 3, primary infantile, B
MONDO:0009992	myoglobinuria, acute recurrent, autosomal recessive
MONDO:0044322	intellectual developmental disorder with neuropsychiatric features
MONDO:0044321	structural heart defects and renal anomalies syndrome
MONDO:0007330	congenital pseudoarthrosis of clavicle
MONDO:0009991	Rh deficiency syndrome
MONDO:0009990	Revesz syndrome
MONDO:0019309	late-onset junctional epidermolysis bullosa
MONDO:0010970	cardiac malformation, cleft lip/palate, microcephaly, and digital anomalies
MONDO:0010972	hydrocephalus-costovertebral dysplasia-Sprengel anomaly syndrome
MONDO:0044317	premature ovarian failure 13
MONDO:0019306	congenital non-bullous ichthyosiform erythroderma
MONDO:0010971	infundibulopelvic stenosis-multicystic kidney syndrome
MONDO:0019305	immune deficiency with skin involvement
MONDO:0044316	thrombocytopenia, anemia, and myelofibrosis
MONDO:0019308	junctional epidermolysis bullosa inversa
MONDO:0010974	nephrotic syndrome, type 2
MONDO:0044319	intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies
MONDO:0010973	autosomal dominant nonsyndromic deafness 5
MONDO:0044318	intellectual developmental disorder with gastrointestinal difficulties and high pain threshold
MONDO:0019307	generalized junctional epidermolysis bullosa non-Herlitz type
MONDO:0019302	mucopolysaccharidosis with skin involvement
MONDO:0019301	metabolic disease with skin involvement
MONDO:0019304	rare photodermatosis
MONDO:0022945	deafness peripheral neuropathy arterial disease
MONDO:0019303	premature aging syndrome
MONDO:0022946	deafness progressive cataract autosomal dominant
MONDO:0022948	Deal Barratt Dillon syndrome
MONDO:0019300	rare skin tumor or hamartoma
MONDO:0022949	defective apolipoprotein b-100
MONDO:0019371	narcolepsy without cataplexy
MONDO:0020360	complete cryptophthalmia
MONDO:0019370	vulvovaginal gingival syndrome
MONDO:0019373	desmoplastic small round cell tumor
MONDO:0019372	solitary bone cyst
MONDO:0020368	Axenfeld anomaly
MONDO:0020367	juvenile open angle glaucoma
MONDO:0007388	congenitally short costocoracoid ligament
MONDO:0020366	congenital glaucoma
MONDO:0020365	congenital hereditary endothelial dystrophy type I
MONDO:0007389	spondylocostal dysostosis 5
MONDO:0007386	human coronavirus sensitivity
MONDO:0020364	posterior polymorphous corneal dystrophy
MONDO:0007387	Cornelia de Lange syndrome 1
MONDO:0020363	honey-droplet corneal dystrophy
MONDO:0007384	congenital trigeminal anesthesia
MONDO:0020362	inverse Marcus-Gunn phenomenon
MONDO:0020361	partial cryptophthalmia
MONDO:0007385	idiopathic spontaneous coronary artery dissection
MONDO:0007382	Ramos-Arroyo syndrome
MONDO:0007383	Stern-Lubinsky-Durrie syndrome
MONDO:0007380	lattice corneal dystrophy type I
MONDO:0007381	epithelial recurrent erosion dystrophy
MONDO:0020359	congenital symblepharon
MONDO:0020358	coloboma of optic disc
MONDO:0019379	st. Louis encephalitis
MONDO:0019378	la Crosse encephalitis
MONDO:0019375	megalencephaly-polymicrogyria-postaxial polydactyly-hydrocephalus syndrome
MONDO:0019374	CAMOS syndrome
MONDO:0019377	Mycoplasma encephalitis
MONDO:0019376	West-Nile encephalitis
MONDO:0019360	rickettsialpox
MONDO:0019362	epidemic louse-borne typhus
MONDO:0019361	boutonneuse fever
MONDO:0020357	coloboma of eyelid
MONDO:0020356	coloboma of iris
MONDO:0020355	coloboma of eye lens
MONDO:0007399	TWIST1-related craniosynostosis
MONDO:0020354	coloboma of choroid and retina
MONDO:0020353	von Hippel anomaly
MONDO:0007397	craniometaphyseal dysplasia, autosomal dominant
MONDO:0007398	craniorhiny
MONDO:0020352	multiple system atrophy, parkinsonian type
MONDO:0007395	craniofacial-deafness-hand syndrome
MONDO:0020351	Blake pouch cyst
MONDO:0020350	Miller-Fisher syndrome
MONDO:0007396	dysostosis, Stanescu type
MONDO:0007393	cranioacrofacial syndrome
MONDO:0007394	craniodiaphyseal dysplasia
MONDO:0007391	coxa vara
MONDO:0007392	coxoauricular syndrome
MONDO:0020349	acute motor axonal neuropathy
MONDO:0007390	coumarin resistance
MONDO:0020348	acute motor and sensory axonal neuropathy
MONDO:0020347	acute inflammatory demyelinating polyradiculoneuropathy
MONDO:0019368	florid cemento-osseous dysplasia
MONDO:0019367	regional odontodysplasia
MONDO:0019369	complex regional pain syndrome
MONDO:0019364	pseudotyphus of California
MONDO:0019363	murine typhus
MONDO:0019366	free sialic acid storage disease
MONDO:0019365	scrub typhus
MONDO:0019351	isolated spina bifida
MONDO:0019350	hereditary spherocytosis
MONDO:0007368	familial benign copper deficiency
MONDO:0020346	synaptic congenital myasthenic syndrome
MONDO:0007369	hereditary coproporphyria
MONDO:0020345	presynaptic congenital myasthenic syndrome
MONDO:0007366	seizures, benign familial neonatal, 2
MONDO:0020344	postsynaptic congenital myasthenic syndrome
MONDO:0020343	alpha-crystallinopathy
MONDO:0007367	febrile seizures, familial, 1
MONDO:0020342	congenital myopathy with excess of thin filaments
MONDO:0007364	arthrogryposis, distal, type 2E
MONDO:0007365	seizures, benign familial neonatal, 1
MONDO:0020341	periventricular nodular heterotopia
MONDO:0020340	bilateral perisylvian polymicrogyria
MONDO:0007362	cone-rod dystrophy 2
MONDO:0007363	congenital contractural arachnodactyly
MONDO:0007360	branchiootic syndrome 2
MONDO:0007361	C1 inhibitor deficiency
MONDO:0020339	X-linked complex spastic paraplegia
MONDO:0020338	adult pure red cell aplasia
MONDO:0020337	congenital dyserythropoietic anemia type 1
MONDO:0020336	autosomal dominant Emery-Dreifuss muscular dystrophy
MONDO:0019357	congenital narrowing of cervical spinal canal
MONDO:0022998	distal arthrogryposis Moore weaver type
MONDO:0019356	urogenital tract malformation
MONDO:0022999	distichiasis heart congenital anomalies
MONDO:0019359	Rocky mountain spotted fever
MONDO:0019358	encephalopathy due to sulfite oxidase deficiency
MONDO:0019353	Stargardt disease
MONDO:0019352	sporotrichosis
MONDO:0019355	adult-onset Still disease
MONDO:0019354	Stickler syndrome
MONDO:0022990	diphallus rachischisis imperforate anus
MONDO:0022991	diploid-triploid mosaicism
MONDO:0019340	scleroderma
MONDO:0022993	dipsogenic diabetes insipidus
MONDO:0007379	Meesmann corneal dystrophy
MONDO:0020335	desquamative interstitial pneumonia
MONDO:0020334	mast cell leukemia
MONDO:0007377	granular corneal dystrophy type I
MONDO:0020333	aggressive systemic mastocytosis
MONDO:0020332	systemic mastocytosis with an associated clonal hematologic non-mast cell lineage disease
MONDO:0007378	posterior polymorphous corneal dystrophy 1
MONDO:0007375	epithelial basement membrane dystrophy
MONDO:0020331	indolent systemic mastocytosis
MONDO:0007376	fleck corneal dystrophy
MONDO:0020330	classic Hodgkin lymphoma, lymphocyte-depleted type
MONDO:0007373	corneal degeneration, ribbonlike, with deafness
MONDO:0007374	Schnyder corneal dystrophy
MONDO:0007371	cornea guttata with anterior polar cataracts
MONDO:0007372	cornea plana 1, autosomal dominant
MONDO:0007370	coracoclavicular joint, anomalous
MONDO:0020329	classic Hodgkin lymphoma, lymphocyte-rich type
MONDO:0020328	classic Hodgkin lymphoma, mixed cellularity type
MONDO:0019349	Sotos syndrome
MONDO:0020327	classic Hodgkin lymphoma, nodular sclerosis type
MONDO:0020326	lymphomatoid papulosis
MONDO:0020325	anaplastic large cell lymphoma
MONDO:0019346	sialidosis type 1
MONDO:0019345	shigellosis
MONDO:0022989	diomedi bernardi placidi syndrome
MONDO:0019348	Ehlers-Danlos syndrome with periventricular heterotopia
MONDO:0019347	peeling skin syndrome
MONDO:0019342	Seckel syndrome
MONDO:0019341	tuberous sclerosis complex
MONDO:0019344	antisynthetase syndrome
MONDO:0019343	mixed connective tissue disease
MONDO:0007429	optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy
MONDO:0007427	deafness with anhidrotic ectodermal dysplasia
MONDO:0007428	deafness-craniofacial syndrome
MONDO:0007425	deafness, sensorineural, with peripheral neuropathy and arterial disease
MONDO:0007426	deafness, unilateral
MONDO:0020401	congenital unguarded mitral orifice
MONDO:0007423	deafness, mid-tone neural
MONDO:0020400	congenital supravalvular mitral ring
MONDO:0007424	autosomal dominant nonsyndromic deafness 1
MONDO:0007421	deafness-ear malformation-facial palsy syndrome
MONDO:0007422	keratoderma hereditarium mutilans
MONDO:0007420	autosomal dominant deafness - onychodystrophy syndrome
MONDO:0019419	X-linked intellectual disability-macrocephaly-macroorchidism syndrome
MONDO:0019416	X-linked intellectual disability-hypogammaglobulinemia-progressive neurological deterioration syndrome
MONDO:0019415	fetal and neonatal alloimmune thrombocytopenia
MONDO:0019418	X-linked intellectual disability-epilepsy-progressive joint contractures-dysmorphism syndrome
MONDO:0019417	X-linked intellectual disability-precocious puberty-obesity syndrome
MONDO:0019412	dysspondyloenchondromatosis
MONDO:0019411	genochondromatosis type 1
MONDO:0019414	BRESEK syndrome
MONDO:0019413	ischio-vertebral syndrome
MONDO:0019410	nodulosis-arthropathy-osteolysis syndrome
MONDO:0007438	dentin dysplasia-sclerotic bones syndrome
MONDO:0007439	deoxyribose-5-phosphate aldolase deficiency
MONDO:0007436	dentin dysplasia type I
MONDO:0007437	dentin dysplasia type II
MONDO:0007434	primary failure of tooth eruption
MONDO:0007435	dentatorubral-pallidoluysian atrophy
MONDO:0007432	cerebral arteriopathy with subcortical infarcts and leukoencephalopathy
MONDO:0007433	dementia/parkinsonism with non-Alzheimer amyloid plaques
MONDO:0007430	dens evaginatus
MONDO:0007431	dens in dente and palatal invaginations
MONDO:0019409	idiopathic juvenile osteoporosis
MONDO:0019408	Astley-Kendall dysplasia
MONDO:0019405	facial onset sensory and motor neuronopathy
MONDO:0019404	perineurioma
MONDO:0019407	microcephalic osteodysplastic dysplasia, Saul-Wilson type
MONDO:0019406	craniofacial conodysplasia
MONDO:0019401	sporadic idiopathic steroid-resistant nephrotic syndrome
MONDO:0019400	testicular seminomatous germ cell tumor
MONDO:0019403	congenital dyserythropoietic anemia
MONDO:0019402	beta thalassemia
MONDO:0007409	cryptomicrotia-brachydactyly-excess fingertip arch syndrome
MONDO:0007407	Cryoglobulinemic vasculitis
MONDO:0007408	cryptotia, familial
MONDO:0007405	Crouzon syndrome
MONDO:0007406	cryofibrinogenemia, familial primary
MONDO:0007403	inherited Creutzfeldt-Jakob disease
MONDO:0007404	Cri-du-chat syndrome
MONDO:0007401	craniosynostosis-Dandy-Walker malformation-hydrocephalus syndrome
MONDO:0007402	creatine phosphokinase, elevated serum
MONDO:0007400	Jackson-Weiss syndrome
MONDO:0007418	Darwinian tubercle of pinna
MONDO:0007419	Darwinian tubercle of pinna
MONDO:0007416	Balkan nephropathy
MONDO:0007417	Darier disease
MONDO:0007414	Gorham-Stout disease
MONDO:0007415	mitochondrial complex III deficiency nuclear type 1
MONDO:0007412	Beare-Stevenson cutis gyrata syndrome
MONDO:0007413	Cyprus facial-neuromusculoskeletal syndrome
MONDO:0007410	isolated cryptophthalmia
MONDO:0007411	cutis laxa, autosomal dominant 1
MONDO:0044250	tongue curling, folding, or rolling
MONDO:0020283	uveitis
MONDO:0019294	mixed dermis disorder
MONDO:0019293	skin vascular disease
MONDO:0020282	metabolic disease with macular cherry-red spot
MONDO:0020281	metabolic disease with pigmentary retinitis
MONDO:0019296	subcutaneous tissue disease
MONDO:0044252	skin/hair/eye pigmentation, variation in, 6
MONDO:0020280	metabolic disease with cataract
MONDO:0044251	australia antigen
MONDO:0019295	other dermis disorder
MONDO:0019290	hypopigmentation of the skin
MONDO:0019292	dermis elastic tissue disorder
MONDO:0019291	rare genetic dermis disorder
MONDO:0044258	methane production
MONDO:0044257	lutheran null
MONDO:0020289	congenital tricuspid malformation
MONDO:0020288	atrioventricular valve anomaly
MONDO:0044259	skin/hair/eye pigmentation, variation in, 2
MONDO:0044254	dermatoglyphics--hypothenar radial arch
MONDO:0020287	pulmonary artery or pulmonary branch anomaly
MONDO:0044253	dermatoglyphics--palmar triradius d, absence of
MONDO:0020286	aortic malformation
MONDO:0044256	skin/hair/eye pigmentation, variation in, 5
MONDO:0020285	transposition of the great arteries and conotruncal cardiac anomaly
MONDO:0020284	heart position anomaly
MONDO:0044255	skin/hair/eye pigmentation, variation in, 1
MONDO:0019298	rare urticaria
MONDO:0019297	lymphedema
MONDO:0019299	unclassified genetic skin disorder
MONDO:0019283	nail anomaly
MONDO:0020272	connective tissue disease with eye involvement
MONDO:0044261	menoq1
MONDO:0044260	ec1
MONDO:0019282	syndromic hair shaft abnormality
MONDO:0020271	phakomatosis with eye involvement
MONDO:0044263	lutheran suppressor, x-linked
MONDO:0020270	pigmentation disorder with eye involvement
MONDO:0019285	syndromic nail anomaly
MONDO:0044262	cyanide, inability to smell
MONDO:0019284	inherited isolated nail anomaly
MONDO:0019281	isolated genetic hair shaft abnormality
MONDO:0019280	hypertrichosis
MONDO:0044269	novelty seeking personality trait
MONDO:0044268	transsexuality
MONDO:0020279	metabolic disease with corneal opacity
MONDO:0020278	metabolic disease associated with ocular features
MONDO:0020277	ectodermal malformation syndrome associated with ocular features
MONDO:0020276	pigmentation disorder with eye involvement, excluding albinism
MONDO:0044265	tooth size
MONDO:0044264	radial loop, plain, on right index finger
MONDO:0020275	oculocutaneous or ocular albinism
MONDO:0044267	gcy
MONDO:0020274	onycho-patellar syndrome with eye involvement
MONDO:0044266	xm system
MONDO:0020273	disease with potential neoplastic degeneration associated with ocular features
MONDO:0019287	ectodermal dysplasia syndrome
MONDO:0019286	sebaceous gland anomaly
MONDO:0019289	hyperpigmentation of the skin
MONDO:0019288	skin pigmentation disease
MONDO:0019272	hereditary palmoplantar keratoderma
MONDO:0020261	neurological disease with abnormal eye movements
MONDO:0044272	body mass index quantitative trait locus 9
MONDO:0044271	bone mineral density quantitative trait locus 1
MONDO:0019271	acrokeratoderma
MONDO:0020260	myasthenic syndrome with eye involvement
MONDO:0019274	other epidermal disorder
MONDO:0044274	hemoglobin, high altitude adaptation
MONDO:0044273	hypertension, diastolic, resistance to
MONDO:0019273	porokeratosis
MONDO:0044270	bilirubin, serum level of, quantitative trait locus 1
MONDO:0019270	erythrokeratoderma
MONDO:0020269	syndromic ichthyosis associated with ocular features
MONDO:0044279	bone mineral density quantitative trait locus 15
MONDO:0020268	ichthyosis associated with ocular features
MONDO:0007289	cataract 13 with adult I phenotype
MONDO:0020267	genetic keratinization disorder associated with ocular features
MONDO:0020266	genodermatosis with ocular features
MONDO:0020265	mitochondrial disease with eye involvement
MONDO:0044276	skin/hair/eye pigmentation, variation in, 11
MONDO:0007287	cataract 41
MONDO:0007288	cataract 6 multiple types
MONDO:0020264	spinocerebellar degenerescence and spastic paraparesis with an oculomotor anomaly
MONDO:0044275	carotid intimal medial thickness 1
MONDO:0007285	cataract 1 multiple types
MONDO:0044278	short sleeper
MONDO:0020263	spinocerebellar ataxia with oculomotor anomaly
MONDO:0007286	cataract 30
MONDO:0044277	uric acid concentration, serum, quantitative trait locus 4
MONDO:0020262	nervous system anomaly with eye involvement
MONDO:0007283	cataract 42
MONDO:0007284	cataract 20 multiple types
MONDO:0007281	cataract 4 multiple types
MONDO:0007282	cataract 29
MONDO:0007280	cataract 8 multiple types
MONDO:0020259	myopathy with eye involvement
MONDO:0019279	alopecia
MONDO:0019276	inherited epidermolysis bullosa
MONDO:0019275	other genetic epidermal disease
MONDO:0019278	hair anomaly
MONDO:0019277	epidermal appendage anomaly
MONDO:0020250	autosomal dominant optic atrophy
MONDO:0019261	infantile neuronal ceroid lipofuscinosis
MONDO:0044283	body mass index quantitative trait locus 18
MONDO:0019260	adult neuronal ceroid lipofuscinosis
MONDO:0044282	blood group, vel system
MONDO:0019263	autosomal erythropoietic protoporphyria
MONDO:0019262	juvenile neuronal ceroid lipofuscinosis
MONDO:0044284	blood group, gerbich system
MONDO:0044281	c3hex, ability to smell
MONDO:0044280	glycerol quantitative trait locus
MONDO:0020258	oculomotor apraxia or related oculomotor disease
MONDO:0020257	supranuclear oculomotor palsy
MONDO:0020256	congenital trochlear nerve palsy
MONDO:0020255	oculomotor palsy
MONDO:0007298	spinocerebellar ataxia type 29
MONDO:0020254	craniostenosis associated with a strabismus
MONDO:0020253	syndrome with a symptomatic strabismus
MONDO:0007299	Sotos syndrome 1
MONDO:0007296	spinocerebellar ataxia type 31
MONDO:0020252	essential strabismus
MONDO:0020251	rare strabismus and restriction syndrome
MONDO:0007297	ADan amyloidosis
MONDO:0007294	central core myopathy
MONDO:0007295	rolandic epilepsy
MONDO:0007292	celiac artery stenosis from compression by median arcuate ligament of diaphragm
MONDO:0007293	leukocyte adhesion deficiency 1
MONDO:0007290	cataract 5 multiple types
MONDO:0007291	familial cerebral cavernous malformation
MONDO:0020249	hereditary optic neuropathy
MONDO:0020248	vitreoretinal degeneration
MONDO:0019269	ichthyosis
MONDO:0019268	epidermal disease
MONDO:0019265	diazoxide-resistant focal hyperinsulinism
MONDO:0019264	alpha-N-acetylgalactosaminidase deficiency type 3
MONDO:0019267	vitamin B12-unresponsive methylmalonic acidemia type mut-
MONDO:0019266	SAPHO syndrome
MONDO:0044214	androstenone, ability to smell
MONDO:0044213	acute idiopathic urticaria
MONDO:0044216	artichoke, modification of taste by
MONDO:0044215	arm folding preference
MONDO:0044210	thalassemia minor
MONDO:0044212	chronic idiopathic urticaria
MONDO:0044211	idiopathic urticaria
MONDO:0044207	specific granule deficiency 1
MONDO:0044206	otospondylomegaepiphyseal dysplasia, autosomal recessive
MONDO:0044209	disorder of lectin complement activation pathway
MONDO:0044208	specific granule deficiency 2
MONDO:0044225	creatine kinase, brain type, ectopic expression of
MONDO:0044224	apocrine gland secretion, variation 1n
MONDO:0044227	dimples, facial
MONDO:0044226	defective interfering particle induction, control of
MONDO:0044221	blood group--lutheran inhibitor
MONDO:0044220	blood group, 1 system
MONDO:0044223	radin blood group antigen
MONDO:0044222	blood group, p1pk system
MONDO:0044218	beeturia
MONDO:0044217	asparagus, specific smell hypersensitivity
MONDO:0044219	blood group, duffy system
MONDO:0044230	epiblepharon of upper 51d
MONDO:0044236	hepatitis b vaccine, response to
MONDO:0044235	hsr
MONDO:0044238	lunulae of fingernails
MONDO:0044237	hypercholesterolemia suppressor
MONDO:0044232	fingers, relative length of
MONDO:0044231	eyebrow, whorl 1n
MONDO:0044234	hrm2
MONDO:0044233	hair whorl
MONDO:0044229	epiblepharon of lower 51d
MONDO:0044228	eegbqtl
MONDO:0020294	atrial defect and interatrial communication
MONDO:0020293	ascending aorta anomaly
MONDO:0020292	congenital anomaly of the great arteries
MONDO:0044241	mydriatic response to pharmacologic agents
MONDO:0020291	hypoplastic right heart syndrome
MONDO:0044240	musical perfect pitch
MONDO:0020290	atrioventricular septal defect
MONDO:0044247	palmomental reflex
MONDO:0044246	nystagmus, voluntary
MONDO:0044249	alkaline phosphatase, plasma level of, quantitative trait locus 1
MONDO:0020299	spinocerebellar ataxia type 15/16
MONDO:0044248	thiourea tasting
MONDO:0020298	Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15
MONDO:0044243	nail high-sulfur protein
MONDO:0020297	Noonan syndrome and Noonan-related syndrome
MONDO:0044242	mydriasis, congenital
MONDO:0020296	congenital arteriovenous fistula
MONDO:0044245	nailbeds, pigmentation of
MONDO:0020295	congenital pulmonary veins anomaly
MONDO:0044244	nail low-sulfur protein
MONDO:0044239	median-ulnar nerve communications
MONDO:0022862	cormier rustin munnich syndrome
MONDO:0007229	Brachymetatarsus 4
MONDO:0022863	corneal crystals myopathy neuropathy
MONDO:0007227	Sillence syndrome
MONDO:0034846	primary desmosis coli
MONDO:0009889	autosomal recessive polycystic kidney disease
MONDO:0007228	brachymesomelia-renal syndrome
MONDO:0022865	corneal dystrophy ichthyosis microcephaly intellectual disability
MONDO:0010877	Charcot-Marie-Tooth disease type 5
MONDO:0009888	polycystic kidney, cataract, and congenital blindness
MONDO:0020203	pigmented conjunctival lesion
MONDO:0007225	fibular aplasia-ectrodactyly syndrome
MONDO:0007226	brachydactyly-nystagmus-cerebellar ataxia syndrome
MONDO:0020202	conjunctival lymphangiectasia
MONDO:0010876	recessive aplasia cutis congenita of limbs
MONDO:0009887	desquamative interstitial pneumonia
MONDO:0020201	conjunctival telangiectasia
MONDO:0009886	pleoconial myopathy with salt craving
MONDO:0010879	CODAS syndrome
MONDO:0007223	brachydactyly type E1
MONDO:0010878	hereditary spastic paraplegia 6
MONDO:0020200	conjunctival hemangioma or hemolymphangioma
MONDO:0009885	Scott syndrome
MONDO:0007224	brachydactyly, type E, with atrial septal defect, type 2
MONDO:0007221	brachydactyly type C
MONDO:0009884	platelet prostacyclin receptor defect
MONDO:0009883	alpha-2-plasmin inhibitor deficiency
MONDO:0007222	brachydactyly type D
MONDO:0009882	plasma clot retraction factor, deficiency of
MONDO:0007220	brachydactyly type B1
MONDO:0009881	pituitary dwarfism with large sella turcica
MONDO:0010880	telangiectasia, hereditary hemorrhagic, type 2
MONDO:0009880	short stature-pituitary and cerebellar defects-small sella turcica syndrome
MONDO:0010882	aphalangy-syndactyly-microcephaly syndrome
MONDO:0010881	mesomelia-synostoses syndrome
MONDO:0019218	inborn disorder of bile acid synthesis
MONDO:0010884	muscular dystrophy, scapulohumeral
MONDO:0010883	pectus excavatum-macrocephaly-dysplastic nails syndrome
MONDO:0019217	inborn disorder of urea cycle metabolism and ammonia detoxification
MONDO:0010886	2q37 microdeletion syndrome
MONDO:0010885	angiokeratoma corporis diffusum with arteriovenous fistulas
MONDO:0019219	inborn disorder of neurotransmitter metabolism and transport
MONDO:0019214	inborn carbohydrate metabolic disorder
MONDO:0022855	congenital vagal hyperreflexivity
MONDO:0019213	cerebral organic aciduria
MONDO:0019216	inborn disorder of amino acid absorption and transport
MONDO:0022857	continuous muscle fiber activity hereditary
MONDO:0022858	continuous spike-wave during slow sleep syndrome
MONDO:0019215	classic organic aciduria
MONDO:0022859	cor biloculare
MONDO:0019210	cutaneous neuroendocrine carcinoma
MONDO:0019212	disseminated superficial actinic porokeratosis
MONDO:0019211	isolated congenital anonychia
MONDO:0022850	congenital sucrose isomaltose malabsorption
MONDO:0022851	Dennis-Fairhurst-Moore syndrome
MONDO:0007238	amastia
MONDO:0007239	epidermolytic hyperkeratosis
MONDO:0022854	congenital unilateral pulmonary hypoplasia
MONDO:0009899	polyhydramnios, chronic idiopathic
MONDO:0007236	branchiootorenal syndrome 1
MONDO:0010866	infantile osteopetrosis with neuroaxonal dysplasia
MONDO:0009898	polysaccharide, storage of unusual
MONDO:0007237	familial juvenile hypertrophy of the breast
MONDO:0010865	pseudoaminopterin syndrome
MONDO:0009897	adult polyglucosan body disease
MONDO:0007234	branchial myoclonus with spastic paraparesis and cerebellar ataxia
MONDO:0010868	rippling muscle disease 1
MONDO:0007235	branchiooculofacial syndrome
MONDO:0010867	PARC syndrome
MONDO:0009896	polymyoclonus, infantile
MONDO:0009895	postaxial polydactyly-dental and vertebral anomalies syndrome
MONDO:0007232	autosomal dominant brachyolmia
MONDO:0007233	second branchial cleft anomaly
MONDO:0009894	short-rib thoracic dysplasia 6 with or without polydactyly
MONDO:0010869	motor neuron disease with dementia and ophthalmoplegia
MONDO:0007230	Brachymorphism-onychodysplasia-dysphalangism syndrome
MONDO:0009893	polydactyly, postaxial, type A5
MONDO:0009892	Chuvash polycythemia
MONDO:0007231	brachytelephalangy-dysmorphism-Kallmann syndrome
MONDO:0009891	acquired polycythemia vera
MONDO:0009890	Gillessen-Kaesbach-Nishimura syndrome
MONDO:0010871	succinic acidemia
MONDO:0010870	tibial muscular dystrophy
MONDO:0019207	DEND syndrome
MONDO:0010873	band heterotopia of brain
MONDO:0010872	parotid salivary glands, polycystic dysgenetic disease of
MONDO:0019206	sparse hair-short stature-skin anomalies syndrome
MONDO:0019209	Japanese encephalitis
MONDO:0010875	pachydermodactyly, familial
MONDO:0019208	Bickerstaff brainstem encephalitis
MONDO:0010874	enteropathy, familial, with villous edema and immunoglobulin G2 deficiency
MONDO:0019203	acute interstitial pneumonia
MONDO:0019202	myxofibrosarcoma
MONDO:0019205	trichodysplasia-amelogenesis imperfecta syndrome
MONDO:0022846	congenital nonhemolytic jaundice
MONDO:0019204	respiratory bronchiolitis-interstitial lung disease syndrome
MONDO:0022849	congenital stenosis of cervical medullary canal
MONDO:0019201	thyrotoxic periodic paralysis
MONDO:0019200	retinitis pigmentosa
MONDO:0007209	Weismann-Netter syndrome
MONDO:0007207	Böök syndrome
MONDO:0007208	Boomerang dysplasia
MONDO:0009869	isolated Pierre-Robin syndrome
MONDO:0022841	congenital hypotrichosis milia
MONDO:0009868	glycogen storage disease IXb
MONDO:0007205	diaphyseal medullary stenosis-bone malignancy syndrome
MONDO:0022843	congenital mumps
MONDO:0009867	lethal congenital glycogen storage disease of heart
MONDO:0007206	bone pain, periodic
MONDO:0010855	short tarsus-absence of lower eyelashes syndrome
MONDO:0009866	phosphoenolpyruvate carboxykinase deficiency, cytosolic
MONDO:0007203	blue rubber bleb nevus
MONDO:0009865	glycogen storage disease due to phosphoglycerate mutase deficiency
MONDO:0007204	Cole-Carpenter syndrome 1
MONDO:0010854	Toriello-Lacassie-Droste syndrome
MONDO:0009864	phosphoenolpyruvate carboxykinase deficiency, mitochondrial
MONDO:0007201	blepharophimosis, ptosis, and epicanthus inversus syndrome
MONDO:0010857	semantic dementia
MONDO:0009863	BH4-deficient hyperphenylalaninemia A
MONDO:0010856	autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis
MONDO:0007202	blepharoptosis-myopia-ectopia lentis syndrome
MONDO:0009862	dihydropteridine reductase deficiency
MONDO:0010859	atrioventricular septal defect 3
MONDO:0010858	macrocephaly-spastic paraplegia-dysmorphism syndrome
MONDO:0009861	phenylketonuria
MONDO:0007200	blepharonasofacial malformation syndrome
MONDO:0009860	phenformin 4-hydroxylation
MONDO:0010860	autosomal recessive nonsyndromic deafness 3
MONDO:0010862	type 1 diabetes mellitus 4
MONDO:0010861	type 1 diabetes mellitus 3
MONDO:0010864	type 1 diabetes mellitus 7
MONDO:0010863	type 1 diabetes mellitus 5
MONDO:0022839	congenital human immunodeficiency virus
MONDO:0007218	brachydactyly type A4
MONDO:0007219	brachydactyly type A6
MONDO:0007216	brachydactyly type A2
MONDO:0022831	congenital heart disease ptosis hypodontia craniostosis
MONDO:0009879	short stature due to growth hormone qualitative anomaly
MONDO:0007217	brachydactyly type A3
MONDO:0009878	pituitary hormone deficiency, combined, 2
MONDO:0022832	congenital heart disease radio ulnar synostosis intellectual disability
MONDO:0009877	Laron syndrome
MONDO:0007214	brachydactyly-preaxial hallux varus syndrome
MONDO:0044203	foveal hypoplasia
MONDO:0010844	epiphyseal dysplasia, multiple, 2
MONDO:0007215	brachydactyly type A1
MONDO:0009876	isolated growth hormone deficiency type IA
MONDO:0010843	dyslexia, susceptibility to, 2
MONDO:0044202	episodic kinesigenic dyskinesia
MONDO:0010846	exostoses, multiple, type III
MONDO:0009875	achromatopsia 3
MONDO:0044205	Shwachman-Diamond syndrome 2
MONDO:0007212	brachydactyly-long thumb syndrome
MONDO:0007213	Ballard syndrome
MONDO:0009874	Rabson-Mendenhall syndrome
MONDO:0044204	Shwachman-Diamond syndrome 1
MONDO:0010845	macrothrombocytopenia and progressive sensorineural deafness
MONDO:0009873	pilodental dysplasia-refractive errors syndrome
MONDO:0010848	spinocerebellar ataxia type 5
MONDO:0007210	Brachmann-de Lange-like facial changes with microcephaly, metatarsus adductus, and developmental delay
MONDO:0007211	brachydactyly-arterial hypertension syndrome
MONDO:0010847	spinocerebellar ataxia type 4
MONDO:0009872	Bjornstad syndrome
MONDO:0009871	pili torti-developmental delay-neurological abnormalities syndrome
MONDO:0044201	T+ B+ severe combined immunodeficiency
MONDO:0010849	palmoplantar keratoderma, Bothnian type
MONDO:0044200	T-B+ severe combined immunodeficiency
MONDO:0009870	pili torti
MONDO:0010851	Lowry-MacLean syndrome
MONDO:0010850	Tessier number 4 facial cleft
MONDO:0010853	Helicobacter pylori infection, susceptibility to
MONDO:0010852	chromosome 8Q12.1-q21.2 deletion syndrome
MONDO:0022822	congenital cardiovascular shunt
MONDO:0022823	congenital contractures
MONDO:0022824	congenital craniosynostosis maternal hyperthyroiditis
MONDO:0022825	congenital cystic eye
MONDO:0022826	congenital cystic eye multiple ocular and intracranial anomalies
MONDO:0019250	inborn disorder of biogenic amine metabolism and transport
MONDO:0019252	other metabolic disease with skin involvement
MONDO:0019251	oligosaccharidosis
MONDO:0007269	dilated cardiomyopathy 1A
MONDO:0020247	congenital vitreoretinal dysplasia
MONDO:0020246	inherited vitreoretinopathy
MONDO:0007267	hypertrophic cardiomyopathy 3
MONDO:0020245	disease predisposing to age-related macular degeneration
MONDO:0007268	hypertrophic cardiomyopathy 4
MONDO:0020244	unclassified primitive or secondary maculopathy
MONDO:0007265	cardiofaciocutaneous syndrome 1
MONDO:0020243	colobomatous and areolar dystrophy
MONDO:0007266	hypertrophic cardiomyopathy 2
MONDO:0020242	genetic macular dystrophy
MONDO:0020241	unclassified familial retinal dystrophy
MONDO:0007263	cardiac rhythm disease
MONDO:0007264	sudden cardiac arrest
MONDO:0020240	syndromic retinitis pigmentosa
MONDO:0007261	Carabelli anomaly of maxillary molar teeth
MONDO:0007262	carcinoid syndrome
MONDO:0007260	Car factor deficiency
MONDO:0020239	color-vision disease
MONDO:0020238	inherited vitreous-retinal disease
MONDO:0020237	lens shape anomaly
MONDO:0019258	mild phenylketonuria
MONDO:0022899	crawfurd syndrome
MONDO:0019257	hemochromatosis type 2
MONDO:0019259	classic phenylketonuria
MONDO:0019254	inborn disorder of purine or pyrimidine metabolism
MONDO:0019253	metabolic disease involving other neurotransmitter deficiency
MONDO:0019256	sterol metabolism disorder
MONDO:0019255	sphingolipidosis
MONDO:0022891	craniosynostosis Maroteaux Fonfria type
MONDO:0022892	craniosynostosis alopecia brain defect
MONDO:0019241	inborn disorder of the gamma-glutamyl cycle
MONDO:0022893	craniosynostosis arthrogryposis cleft palate
MONDO:0019240	sterol biosynthesis disorder
MONDO:0022894	craniosynostosis autosomal dominant
MONDO:0022895	craniosynostosis cleft lip palate arthrogryposis
MONDO:0022896	craniosynostosis contractures cleft
MONDO:0022897	craniosynostosis exostoses nevus epibulbar dermoid
MONDO:0022898	craniosynostosis intellectual disability heart defects
MONDO:0020236	lens position anomaly
MONDO:0020235	lens size anomaly
MONDO:0007278	cataract 32 multiple types
MONDO:0020234	craniofacial anomaly with cataract
MONDO:0020233	dentocutaneous disease with cataract
MONDO:0007279	cataract 7
MONDO:0007276	cat-eye syndrome
MONDO:0020232	musculoskeletal disease with cataract
MONDO:0007277	cataract-aberrant oral frenula-growth delay syndrome
MONDO:0020231	cardiac disease with cataract
MONDO:0007274	carpal displacement
MONDO:0020230	renal disease with cataract
MONDO:0007275	carpal tunnel syndrome
MONDO:0022890	craniosynostosis Fontaine type
MONDO:0007272	hereditary hypercarotenemia and vitamin A deficiency
MONDO:0007273	paragangliomas 4
MONDO:0007270	cardiomyopathy, familial restrictive, 1
MONDO:0007271	familial cutaneous collagenoma
MONDO:0020229	cerebral disease with cataract
MONDO:0020228	cataract associated with a metabolic disease
MONDO:0020227	systemic disease with cataract
MONDO:0020226	chromosomal anomaly with cataract
MONDO:0022888	craniostenosis cataract
MONDO:0019247	combined hyperlipidemia (including acquired and inherited)
MONDO:0019246	inborn disorder of lysosomal amino acid transport
MONDO:0022889	craniostenosis with congenital heart disease intellectual disability
MONDO:0019249	mucopolysaccharidosis
MONDO:0019248	mucolipidosis
MONDO:0019243	inborn disorder of energy metabolism
MONDO:0019242	inborn disorder of branched-chain amino acid metabolism
MONDO:0019245	lysosomal lipid storage disorder
MONDO:0019244	glycogen storage disease
MONDO:0022880	corticobasal degeneration
MONDO:0019230	inborn disorder of ornithine or proline metabolism
MONDO:0022883	craniofacial and skeletal defects
MONDO:0022884	craniofacial dysostosis arthrogryposis progeroid appearence
MONDO:0007249	camptobrachydactyly
MONDO:0022887	craniofrontonasal syndrome Teebi type
MONDO:0020225	syndromic cataract
MONDO:0007247	basal ganglia calcification, idiopathic, childhood-onset
MONDO:0010899	autosomal dominant nocturnal frontal lobe epilepsy 1
MONDO:0020224	rare cataract
MONDO:0007248	hereditary painful callosities
MONDO:0010898	Autosomal dominant epilepsy with auditory features
MONDO:0007245	neurofibromatosis type 6
MONDO:0020223	lens and zonula anomaly
MONDO:0007246	calcific aortic disease with immunologic abnormalities, familial
MONDO:0020222	rare disease with glaucoma as a major feature
MONDO:0007243	Burkitt lymphoma
MONDO:0020221	secondary glaucoma due to a proliferation and differentiation anomaly
MONDO:0007244	Caffey disease
MONDO:0020220	corneoiridogoniodysgenesis
MONDO:0007241	bundle branch block, familial isolated complete right
MONDO:0007242	butyrylesterase 1
MONDO:0007240	progressive familial heart block, type 1A
MONDO:0020219	corneogoniodysgenesis
MONDO:0020218	goniodysgenesis
MONDO:0020217	secondary dysgenetic glaucoma associated with neural crest cell migration anomaly
MONDO:0019239	inborn disorder of serine family metabolism
MONDO:0020216	secondary dysgenetic glaucoma
MONDO:0020215	syndromic corneal dystrophy
MONDO:0019236	inborn disorder of purine metabolism
MONDO:0019235	inborn disorder of phenylalanin or tyrosine metabolism
MONDO:0019238	inborn disorder of pyrimidine metabolism
MONDO:0019237	inborn disorder of pyridoxine metabolism
MONDO:0019232	inborn disorder of peptide metabolism
MONDO:0019231	inborn disorder of pentose phosphate metabolism
MONDO:0019234	peroxisome biogenesis disorder
MONDO:0019233	disorder of peroxisomal beta oxidation
MONDO:0022871	corpus callosum agenesis of blepharophimosis robin type
MONDO:0022872	corpus callosum dysgenesis X-linked recessive
MONDO:0022873	corpus callosum dysgenesis cleft spasm
MONDO:0022874	corpus callosum dysgenesis hypopituitarism
MONDO:0022875	cortada Koussef Matsumoto syndrome
MONDO:0022876	Cortes Lacassie syndrome
MONDO:0010888	endometriosis of uterus
MONDO:0020214	posterior corneal dystrophy
MONDO:0007258	canine teeth, absence of upper permanent
MONDO:0020213	stromal corneal dystrophy
MONDO:0007259	craniofaciofrontodigital syndrome
MONDO:0010887	isolated anterior cervical hypertrichosis
MONDO:0007256	hepatocellular carcinoma
MONDO:0020212	superficial corneal dystrophy
MONDO:0020211	syndromic keratoconus
MONDO:0010889	arterial dissection-lentiginosis syndrome
MONDO:0007257	candidiasis, familial, 1
MONDO:0007254	breast cancer
MONDO:0020210	syndromic hyperopia
MONDO:0007255	colorectal cancer
MONDO:0007252	Gordon syndrome
MONDO:0007253	cancer, familial, with in vitro Radioresistance
MONDO:0007250	camptodactyly of fingers
MONDO:0010891	lethal hemolytic anemia-genital anomalies syndrome
MONDO:0007251	campomelic dysplasia
MONDO:0010890	acrocardiofacial syndrome
MONDO:0020209	rare hyperopia and astigmatism
MONDO:0010893	malignant hyperthermia, susceptibility to, 4
MONDO:0020208	syndromic myopia
MONDO:0010892	mitochondrial myopathy and sideroblastic anemia
MONDO:0010895	ABCD syndrome
MONDO:0019229	inborn disorder of ketolysis
MONDO:0020207	rare isolated myopia
MONDO:0020206	rare refraction anomaly
MONDO:0019228	inborn disorder of histidine metabolism
MONDO:0010894	maturity-onset diabetes of the young type 3
MONDO:0020205	bulbar conjunctival dermoid or conjunctival dermolipoma
MONDO:0010897	schizophrenia 3
MONDO:0010896	pigment dispersion syndrome
MONDO:0020204	conjunctival tumor
MONDO:0019225	gluconeogenesis disorder
MONDO:0022866	corneal dystrophy pigmentary anomaly malabsorption
MONDO:0019224	inborn disorder of gamma-aminobutyric acid metabolism
MONDO:0019227	inborn disorder of glycerol metabolism
MONDO:0022869	coronary arteries congenital malformation
MONDO:0019226	glucose transport disorder
MONDO:0019221	creatine deficiency syndrome
MONDO:0019220	inborn disorder of cobalamin metabolism and transport
MONDO:0019223	inborn disorder of fatty acid oxidation and ketone body metabolism
MONDO:0019222	inborn disorder of methionine cycle and sulfur amino acid metabolism
MONDO:0010918	EIG1
MONDO:0009929	neonatal acute respiratory distress due to SP-B deficiency
MONDO:0009928	pulmonary alveolar microlithiasis
MONDO:0010917	chondrocalcinosis 1
MONDO:0009927	3MC syndrome 2
MONDO:0009926	autosomal recessive multiple pterygium syndrome
MONDO:0010919	varicella, severe recurrent
MONDO:0009925	autosomal recessive inherited pseudoxanthoma elasticum
MONDO:0009924	vitamin D-dependent rickets, type 1
MONDO:0009923	46,XY disorder of sex development due to 5-alpha-reductase 2 deficiency
MONDO:0009922	Pseudouridinuria and mental defect
MONDO:0010910	enuresis, nocturnal, 1
MONDO:0009921	holoprosencephaly-postaxial polydactyly syndrome
MONDO:0009920	Acrootoocular syndrome
MONDO:0010912	fibrosis of extraocular muscles, congenital, 3A, with or without extraocular involvement
MONDO:0010911	prolactin-producing pituitary gland adenoma
MONDO:0010914	carnitine palmitoyl transferase II deficiency, severe infantile form
MONDO:0010913	Caroli disease
MONDO:0010916	polycystic kidney disease 3 with or without polycystic liver disease
MONDO:0010915	autosomal dominant nonsyndromic deafness 4A
MONDO:0009919	peroxisomal acyl-CoA oxidase deficiency
MONDO:0010907	familial hypertryptophanemia
MONDO:0010906	orofacial cleft 11
MONDO:0009939	pulmonic stenosis and congenital nephrosis
MONDO:0010909	UV-sensitive syndrome 1
MONDO:0009938	pulmonic stenosis
MONDO:0009937	pulmonary venoocclusive disease
MONDO:0010908	loose anagen syndrome
MONDO:0009936	familial primary pulmonary hypoplasia
MONDO:0009935	pulmonary hypertension, primary, autosomal recessive
MONDO:0009934	alveolar capillary dysplasia with misalignment of pulmonary veins
MONDO:0009933	congenital pulmonary lymphangiectasia
MONDO:0009932	pulmonary bullae causing pneumothorax
MONDO:0009931	pulmonary atresia-intact ventricular septum syndrome
MONDO:0009930	pulmonary arteriovenous malformation
MONDO:0010901	HEC syndrome
MONDO:0010900	intrauterine growth retardation with increased mitomycin c sensitivity
MONDO:0010903	craniosynostosis, Adelaide type
MONDO:0010902	spondyloepiphyseal dysplasia, Reardon type
MONDO:0010905	cone-rod dystrophy 1
MONDO:0010904	setting-Sun phenomenon, familial benign
MONDO:0009907	Prepapillary vascular loops
MONDO:0009906	prenatal bowing
MONDO:0009905	urban-Rogers-Meyer syndrome
MONDO:0009904	Gitelman syndrome
MONDO:0009903	postaxial acrofacial dysostosis
MONDO:0009902	cutaneous porphyria
MONDO:0009901	Bartsocas-Papas syndrome
MONDO:0009900	polysyndactyly-cardiac malformation syndrome
MONDO:0009918	fundus dystrophy, pseudoinflammatory, recessive form
MONDO:0009917	autosomal recessive pseudohypoaldosteronism type 1
MONDO:0009916	46,XY disorder of sex development due to 17-beta-hydroxysteroid dehydrogenase 3 deficiency
MONDO:0009915	46,XX disorder of sex development-skeletal anomalies syndrome
MONDO:0009914	pseudodiastrophic dysplasia
MONDO:0009913	prune belly syndrome with pulmonic stenosis, intellectual disability, and deafness
MONDO:0009912	prolactin deficiency with obesity and enlarged testes
MONDO:0009911	prolactin deficiency, isolated
MONDO:0009910	Wiedemann-Rautenstrauch syndrome
MONDO:0009909	progesterone resistance
MONDO:0009908	pterin-4 alpha-carbinolamine dehydratase 1 deficiency
MONDO:0007308	Charcot-Marie-Tooth disease type 2A1
MONDO:0007309	Charcot-Marie-Tooth disease type 1A
MONDO:0007306	Klippel-Feil syndrome 1, autosomal dominant
MONDO:0009969	renal-genital-middle ear anomalies
MONDO:0009968	renal tubular acidosis, distal, 2, with progressive sensorineural hearing loss
MONDO:0007307	Charcot-Marie-Tooth disease type 1B
MONDO:0022940	deafness hyperuricemia neurologic ataxia
MONDO:0009967	renal tubular acidosis 3
MONDO:0022941	deafness hypospadias metacarpal and metatarsal syndrome
MONDO:0007304	cervical vertebral Bridge
MONDO:0009966	NPHP3-related Meckel-like syndrome
MONDO:0007305	cervical vertebral dysplasia
MONDO:0022942	deafness mesenteric diverticula of small bowel neuropathy
MONDO:0007302	cervical hypertrichosis with underlying kyphoscoliosis
MONDO:0009965	Perlman syndrome
MONDO:0010954	Wiskott-Aldrich syndrome, autosomal dominant form
MONDO:0009964	short-rib thoracic dysplasia 9 with or without polydactyly
MONDO:0007303	cervical rib disease
MONDO:0010953	Fanconi anemia complementation group E
MONDO:0007300	cerebral sarcoma
MONDO:0009963	Ulbright-Hodes syndrome
MONDO:0010956	enamel hypoplasia, cataracts, and aqueductal stenosis
MONDO:0010955	ectodermal dysplasia with intellectual disability and syndactyly
MONDO:0007301	cerebrocostomandibular syndrome
MONDO:0009962	Senior-Loken syndrome 1
MONDO:0010958	cardiac arrhythmia, ankyrin-B-related
MONDO:0009961	renal and mullerian duct hypoplasia
MONDO:0009960	inflammatory bowel disease 1
MONDO:0010957	agonadism, 46,XY, with intellectual disability, short stature, retarded bone age, and multiple extragenital malformations
MONDO:0010959	van den Ende-Gupta syndrome
MONDO:0010961	obesity due to prohormone convertase I deficiency
MONDO:0010960	protocadherin 3
MONDO:0010963	autosomal dominant nonsyndromic deafness 6
MONDO:0010962	diffuse nonepidermolytic palmoplantar keratoderma
MONDO:0022932	Davenport-Donlan syndrome
MONDO:0022934	Davis Lafer syndrome
MONDO:0022936	de Hauwere Leroy adriaenssens syndrome
MONDO:0022937	deafness conductive stapedial ear malformation facial palsy
MONDO:0022938	deafness goiter stippled epiphyses
MONDO:0022939	deafness hyperuricemia neurologic ataxia
MONDO:0007319	chondrocalcinosis 2
MONDO:0007317	chlorpropamide-alcohol flushing
MONDO:0007318	Alagille syndrome
MONDO:0009979	reticular dystrophy of the retinal pigment epithelium
MONDO:0007315	cherubism
MONDO:0009978	retinal degeneration-nanophthalmos-glaucoma syndrome
MONDO:0022930	dandy-walker malformation with nasopharyngeal teratoma and diaphragmatic hernia
MONDO:0007316	Chiari malformation type I
MONDO:0009977	Knobloch syndrome
MONDO:0007313	cheilitis glandularis
MONDO:0009976	retinal degeneration and epilepsy
MONDO:0010943	schizophrenia 4
MONDO:0007314	chemodectoma, intraabdominal, with cutaneous angiolipomas
MONDO:0010942	eukaryotic translation elongation factor 1 alpha-1-like 14
MONDO:0009975	reticulum cell sarcoma
MONDO:0009974	familial hemophagocytic lymphohistiocytosis type 1
MONDO:0007311	Charcot-Marie-Tooth disease type 1E
MONDO:0010945	retinitis pigmentosa 17
MONDO:0010944	mitochondrial import-stimulating factor
MONDO:0007312	Charcot-Marie-Tooth disease with ptosis and parkinsonism
MONDO:0009973	reticular dysgenesis
MONDO:0010947	Budd-Chiari syndrome
MONDO:0009972	respiratory underresponsiveness to hypoxia and hypercapnia
MONDO:0007310	Charcot-Marie-Tooth disease, Guadalajara neuronal type
MONDO:0009971	newborn respiratory distress syndrome
MONDO:0010946	hypertrophic cardiomyopathy 6
MONDO:0010949	Charcot-Marie-Tooth disease type 2B
MONDO:0009970	renal tubular dysgenesis of genetic origin
MONDO:0010948	cataract 10 multiple types
MONDO:0010950	type 1 diabetes mellitus 8
MONDO:0010952	hereditary hyperferritinemia with congenital cataracts
MONDO:0010951	dilated cardiomyopathy 1B
MONDO:0022921	short stature-microcephaly-heart defect syndrome
MONDO:0022926	daentl towsend Siegel syndrome
MONDO:0010939	low phospholipid associated cholelithiasis
MONDO:0009949	pyruvate carboxylase deficiency disease
MONDO:0009948	pyropoikilocytosis, hereditary
MONDO:0009947	glutathione synthetase deficiency with 5-oxoprolinuria
MONDO:0009946	hemolytic anemia due to pyrimidine 5' nucleotidase deficiency
MONDO:0009945	pyridoxine-dependent epilepsy
MONDO:0009944	pyloric atresia
MONDO:0009943	Pyle disease
MONDO:0010932	progressive bifocal chorioretinal atrophy
MONDO:0009942	pyknoachondrogenesis
MONDO:0010931	vitamin D-dependent rickets, type 2B
MONDO:0009941	Pygmy
MONDO:0010934	DFNB5
MONDO:0010933	autosomal recessive nonsyndromic deafness 4
MONDO:0009940	pycnodysostosis
MONDO:0010936	frontotemporal dementia and/or amyotrophic lateral sclerosis 7
MONDO:0010935	neuronopathy, distal hereditary motor, type 5A
MONDO:0010938	T-B+ severe combined immunodeficiency due to JAK3 deficiency
MONDO:0010937	isoproterenol-mediated vasodilatation
MONDO:0022918	cytokine deficiency
MONDO:0022919	cytokine receptor deficiency
MONDO:0010941	nocturnal enuresis, 2
MONDO:0010940	inherited susceptibility to asthma
MONDO:0022912	cutis verticis gyrata mental deficiency
MONDO:0022913	cutler bass Romshe syndrome
MONDO:0022916	cystic hygroma lethal cleft palate
MONDO:0010929	craniosynostosis 4
MONDO:0010928	dwarfism, familial, with muscle spasms
MONDO:0009959	peroxisome biogenesis disorder type 3B
MONDO:0009958	adult Refsum disease
MONDO:0009957	Reese retinal dysplasia
MONDO:0009956	red skin pigment anomaly of new guinea
MONDO:0009955	rapadilino syndrome
MONDO:0010921	nasal dermoid cyst
MONDO:0009954	Ramon syndrome
MONDO:0009953	leukocyte adhesion deficiency type II
MONDO:0010920	microtia
MONDO:0010923	proximal myopathy with focal depletion of mitochondria
MONDO:0009952	radioulnar synostosis-developmental delay-hypotonia syndrome
MONDO:0009951	radiculoneuropathy, fatal neonatal
MONDO:0010922	Satoyoshi syndrome
MONDO:0010925	velo-facial-skeletal syndrome
MONDO:0009950	pyruvate kinase deficiency of red cells
MONDO:0010924	D-2-hydroxyglutaric aciduria
MONDO:0010927	orofacial cleft 3
MONDO:0010926	familial hypocalciuric hypercalcemia 3
MONDO:0022907	cutaneous sclerosis
MONDO:0022908	cutis gyratum acanthosis nigricans craniosynostosis
MONDO:0022909	cutis laxa osteoporosis
MONDO:0010930	anophthalmia plus syndrome
MONDO:0022900	athyreotic congenital hypothyroidism
MONDO:0022901	Crohn disease of the esophagus
MONDO:0022904	cryofibrinogenemia
MONDO:0044299	myasthenic syndrome, congenital, 22
MONDO:0019173	rabies
MONDO:0020162	secondary ectropion
MONDO:0020161	congenital ectropion
MONDO:0019172	aniridia
MONDO:0019175	primary lymphedema
MONDO:0020160	secondary entropion
MONDO:0019174	infantile Refsum disease
MONDO:0019171	familial long QT syndrome
MONDO:0019170	polyarteritis nodosa
MONDO:0044137	vitreous body disorder
MONDO:0020169	rare disorder with ptosis
MONDO:0020168	kinetic eyelid anomaly
MONDO:0020167	malposition of external canthus
MONDO:0044138	hyalitis
MONDO:0007188	primary basilar invagination
MONDO:0020166	telecanthus
MONDO:0007189	B-cell growth factor
MONDO:0020165	syndromic epicanthus
MONDO:0007186	gastroesophageal reflux disease
MONDO:0020164	epicanthal fold
MONDO:0007187	nevoid basal cell carcinoma syndrome
MONDO:0020163	canthal anomaly
MONDO:0007184	alopecia, androgenetic, 1
MONDO:0007185	Banki syndrome
MONDO:0007182	Machado-Joseph disease
MONDO:0007183	azotemia, familial
MONDO:0007180	Axenfeld-Rieger anomaly with partially absent eye muscles, distinctive face, hydrocephaly, and skeletal abnormalities
MONDO:0007181	axial osteomalacia
MONDO:0019177	odontoleukodystrophy
MONDO:0019176	trichorhinophalangeal syndrome type I or III
MONDO:0019179	monosomy 9q22.3
MONDO:0019178	auricular abnormalities-cleft lip with or without cleft palate-ocular abnormalities syndrome
MONDO:0019162	pseudohypoaldosteronism type 2
MONDO:0020151	rare palpebral disease
MONDO:0019161	pseudohypoaldosteronism type 1
MONDO:0020150	obsolete rare palpebral, lacrimal system and conjunctival disease
MONDO:0019164	6q terminal deletion syndrome
MONDO:0019163	pseudoxanthoma elasticum
MONDO:0044141	panic disorder without agoraphobia
MONDO:0019160	primary progressive freezing gait
MONDO:0020159	congenital entropion
MONDO:0020158	eyelids malposition disorder
MONDO:0020157	syndromic palpebral coloboma
MONDO:0020156	syndromic ankyloblepharon
MONDO:0020155	eyelid border anomaly
MONDO:0044144	panic disorder with agoraphobia
MONDO:0007199	blepharochalasis, superior
MONDO:0020154	microblepharon-ablephara syndrome
MONDO:0007197	bladder diverticulum
MONDO:0020153	cryptophthalmia
MONDO:0020152	rare eyelid malformation
MONDO:0007198	Ascher syndrome
MONDO:0007195	bifid nose, autosomal dominant
MONDO:0007196	bladder cancer
MONDO:0007193	primary biliary cholangitis 1
MONDO:0007194	familial bicuspid aortic valve
MONDO:0007191	Behcet disease
MONDO:0007192	beta-amino acids, renal transport of
MONDO:0007190	leukemia, chronic lymphocytic, susceptibility to, 2
MONDO:0020149	rare eye disease due to a differentiation anomaly
MONDO:0019169	pyruvate dehydrogenase deficiency
MONDO:0019166	strongyloidiasis
MONDO:0019165	central precocious puberty
MONDO:0019168	pyomyositis
MONDO:0019167	immunoglobulin a vasculitis
MONDO:0019151	oligocone trichromacy
MONDO:0020140	late-onset ataxia with dementia
MONDO:0019150	familial isolated restrictive cardiomyopathy
MONDO:0019153	brain malformation-congenital heart disease-postaxial polydactyly syndrome
MONDO:0019152	Oguchi disease
MONDO:0020148	syndromic aniridia
MONDO:0020147	anophthalmia-microphthalmia syndrome
MONDO:0007168	atelosteogenesis type III
MONDO:0020146	major induction processes eye anomaly
MONDO:0007169	atherosclerosis susceptibility
MONDO:0020145	developmental defect of the eye
MONDO:0020144	cerebrovascular dementia
MONDO:0007166	ataxia with fasciculations
MONDO:0007167	atelosteogenesis type I
MONDO:0020143	cerebral lipidosis with dementia
MONDO:0007164	spastic ataxia 1
MONDO:0020142	metabolic disease with dementia
MONDO:0007165	spastic ataxia 7
MONDO:0020141	infectious disease with dementia
MONDO:0007162	asymmetric short stature syndrome
MONDO:0007163	episodic ataxia type 2
MONDO:0007160	Stickler syndrome type 1
MONDO:0007161	spermatogenic failure 2
MONDO:0020139	early-onset ataxia with dementia
MONDO:0020138	ataxia with dementia
MONDO:0019159	Loeffler endocarditis
MONDO:0019158	tropical endomyocardial fibrosis
MONDO:0019155	Leydig cell hypoplasia
MONDO:0019154	androgen insensitivity syndrome
MONDO:0019157	acquired idiopathic sideroblastic anemia
MONDO:0019156	angioosteohypotrophic syndrome
MONDO:0019140	acute ackee fruit intoxication
MONDO:0022792	coccygodynia
MONDO:0019142	inherited porphyria
MONDO:0022794	chromosome 8 deletion
MONDO:0022795	deficiency of coenzyme q cytochrome c reductase
MONDO:0019141	porokeratosis of Mibelli
MONDO:0022798	Cohen lockood wyborney syndrome
MONDO:0022799	cold urticaria
MONDO:0020137	frontotemporal degeneration with dementia
MONDO:0020136	neurodegenerative disease with dementia
MONDO:0020135	pontocerebellar hypoplasia
MONDO:0007179	autoimmune disease
MONDO:0020134	cystic malformation of the posterior fossa
MONDO:0007177	auriculoosteodysplasia
MONDO:0020133	posterior fossa malformation
MONDO:0007178	aurocephalosyndactyly
MONDO:0020132	cranial nerve and nuclear aplasia
MONDO:0022790	cleft tongue
MONDO:0007175	PR interval, variation 1N
MONDO:0020131	malformation of the cerebellar hemispheres
MONDO:0007176	helicoid peripapillary chorioretinal degeneration
MONDO:0022791	coarse face hypotonia constipation
MONDO:0020130	malformation of the cerebellar vermis
MONDO:0007173	atrial septal defect 7
MONDO:0007174	Lown-Ganong-Levine syndrome
MONDO:0007171	atrial standstill 1
MONDO:0007172	atrial septal defect 1
MONDO:0020129	acquired motor neuron disease
MONDO:0007170	atresia of external auditory canal and conductive deafness
MONDO:0020128	motor neuron disease
MONDO:0020127	genetic peripheral neuropathy
MONDO:0019148	Wolman disease
MONDO:0019147	myiasis
MONDO:0019149	cholesteryl ester storage disease
MONDO:0019144	hereditary thrombophilia due to congenital protein S deficiency
MONDO:0019143	angiostrongyliasis
MONDO:0019146	inherited susceptibility to mycobacterial diseases
MONDO:0019145	hereditary thrombophilia due to congenital protein C deficiency
MONDO:0020195	excretory apparatus of the lacrimal system anomaly
MONDO:0020194	congenital alacrima
MONDO:0020193	secretory apparatus of the lacrimal system anomaly
MONDO:0020192	rare lacrimal system disease
MONDO:0020191	eyebrow/eyelashes pigmentation anomaly
MONDO:0020190	eyebrow/eyelashes distichiasis
MONDO:0020199	conjunctival vascular anomaly
MONDO:0020198	rare conjunctival disease
MONDO:0020197	EEC syndrome and related syndrome
MONDO:0044101	pregnancy, cornual
MONDO:0020196	anomaly of the secretory and excretory apparatus of the lacrimal system
MONDO:0019195	hereditary inclusion body myopathy-joint contractures-ophthalmoplegia syndrome
MONDO:0020184	rare eyebrow/eyelashes anomaly
MONDO:0019194	localized lipodystrophy
MONDO:0020183	neurogenic palpebral tumor
MONDO:0019197	folinic acid-responsive seizures
MONDO:0020182	palpebral tumor with a vascular malformation
MONDO:0019196	Foix-Alajouanine syndrome
MONDO:0020181	mesenchymatous palpebral tumor
MONDO:0019191	IgG4-related dacryoadenitis and sialadenitis
MONDO:0020180	palpebral piliary tumor
MONDO:0019190	juvenile polyposis of infancy
MONDO:0019193	acquired generalized lipodystrophy
MONDO:0019192	AKT2-related familial partial lipodystrophy
MONDO:0020189	eyebrow/eyelashes structural anomaly
MONDO:0020188	congenital absence of the eyebrow/eyelashes
MONDO:0020187	eyelashes hypertrophy
MONDO:0020186	eyebrow hypertrophy
MONDO:0044113	bullous systemic lupus erythematosus
MONDO:0020185	eyebrow/eyelashes hypertrichosis
MONDO:0019199	interstitial granulomatous dermatitis with arthritis
MONDO:0019198	sympathetic ophthalmia
MONDO:0020173	benign tumor of palpebral epidermis
MONDO:0019184	ankylostomiasis
MONDO:0020172	palpebral epidermal tumor
MONDO:0019183	inherited odontologic disease
MONDO:0019186	Q fever
MONDO:0020171	palpebral tumor
MONDO:0020170	congenital upper palpebral retraction
MONDO:0019185	rhabdomyosarcoma
MONDO:0019180	hereditary hemorrhagic telangiectasia
MONDO:0019182	monogenic obesity
MONDO:0019181	non-syndromic X-linked intellectual disability
MONDO:0020179	palpebral nevus
MONDO:0020178	palpebral lentiginosis
MONDO:0020177	pigmented palpebral tumor
MONDO:0020176	palpebral sebaceous gland tumor
MONDO:0020175	malignant tumor of palpebral epidermis
MONDO:0020174	precancerous lesion of palpebral epidermis
MONDO:0019188	Rubinstein-Taybi syndrome
MONDO:0019187	Axenfeld-Rieger syndrome
MONDO:0019189	inborn disorder of amino acid and other organic acid metabolism
MONDO:0022740	Christian Johnson angenieta syndrome
MONDO:0007108	anal canal carcinoma
MONDO:0007109	congenital dyserythropoietic anemia type 3
MONDO:0022742	occupational asthma
MONDO:0009769	oculo-palato-cerebral syndrome
MONDO:0007106	anal sphincter dysplasia
MONDO:0007107	anal sphincter myopathy, internal
MONDO:0009768	oculodentodigital dysplasia, autosomal recessive
MONDO:0007104	amyotrophic lateral sclerosis-parkinsonism-dementia complex
MONDO:0009767	oculocerebral hypopigmentation syndrome, Cross type
MONDO:0010756	Von Willebrand disease, X-linked form
MONDO:0010755	vesicoureteral reflux, X-linked
MONDO:0007105	frontotemporal dementia and/or amyotrophic lateral sclerosis 1
MONDO:0009766	oculocerebral hypopigmentation syndrome of Preus
MONDO:0007102	amyotrophic dystonic paraplegia
MONDO:0010758	Wieacker-Wolff syndrome
MONDO:0009765	ocular myopathy with curare sensitivity
MONDO:0010757	widow's peak syndrome
MONDO:0007103	amyotrophic lateral sclerosis type 1
MONDO:0009764	ocular motor apraxia, Cogan type
MONDO:0007100	familial amyloid neuropathy
MONDO:0009763	obesity-hypoventilation syndrome
MONDO:0007101	familial primary localized cutaneous amyloidosis
MONDO:0009762	nystagmus, congenital, autosomal recessive
MONDO:0010759	Wildervanck syndrome
MONDO:0009761	cystic hygroma
MONDO:0009760	Norman-Roberts syndrome
MONDO:0010761	retinitis pigmentosa Y-linked
MONDO:0010760	XH antigen
MONDO:0010763	spermatogenic failure, Y-linked, 1
MONDO:0010762	lymphoma, Hodgkin, Y-linked pseudoautosomal
MONDO:0010765	46,XY complete gonadal dysgenesis
MONDO:0010764	deafness, Y-linked 1
MONDO:0022734	chorioretinopathy dominant form microcephaly
MONDO:0022735	choroid plexus cyst
MONDO:0022736	occupational lung disease
MONDO:0022737	choroideremia hypopituitarism
MONDO:0022739	Christian demyer franken syndrome
MONDO:0007119	isolated aniridia
MONDO:0022732	chorea minor
MONDO:0007117	angioedema, hereditary, type 1/2
MONDO:0009779	autosomal recessive omodysplasia
MONDO:0022733	choreoacanthocytosis amyotrophic
MONDO:0007118	isolated anhidrosis with normal sweat glands
MONDO:0010745	beta-thalassemia-X-linked thrombocytopenia syndrome
MONDO:0009778	olivopontocerebellar atrophy II, autosomal recessive
MONDO:0007115	angioma serpiginosum, autosomal dominant
MONDO:0009777	Oliver syndrome
MONDO:0007116	hereditary neurocutaneous angioma
MONDO:0010744	thrombocytopenia with elevated serum IgA and renal disease
MONDO:0009776	spermatogenic failure 1
MONDO:0007113	Angelman syndrome
MONDO:0010747	X-linked dystonia-parkinsonism
MONDO:0007114	angel-shaped phalango-epiphyseal dysplasia
MONDO:0010746	thumbs, congenital Clasped
MONDO:0009775	Oguchi disease-1
MONDO:0009774	cloacal exstrophy
MONDO:0010749	trigonocephaly-short stature-developmental delay syndrome
MONDO:0007111	aneurysm, intracranial berry type 1
MONDO:0010748	torticollis-keloids-cryptorchidism-renal dysplasia syndrome
MONDO:0009773	odonto-onycho-dermal dysplasia
MONDO:0007112	interventricular septum aneurysm
MONDO:0009772	oculorenocerebellar syndrome
MONDO:0007110	Diamond-Blackfan anemia 1
MONDO:0009771	oculotrichodysplasia
MONDO:0009770	3MC syndrome 1
MONDO:0010750	ulnar hypoplasia-split foot syndrome
MONDO:0010752	VACTERL association, X-linked, with or without hydrocephalus
MONDO:0010751	unique green phenomenon
MONDO:0010754	van den Bosch syndrome
MONDO:0010753	cardiac valvular dysplasia, X-linked
MONDO:0022723	chondrodysplasia
MONDO:0022725	chondrodysplasia lethal recessive
MONDO:0022729	chondrodysplasia punctata with steroid sulfatase deficiency
MONDO:0009749	giant axonal neuropathy 1
MONDO:0009748	hereditary sensory and autonomic neuropathy with spastic paraplegia
MONDO:0009747	Navajo neurohepatopathy
MONDO:0009746	hereditary sensory and autonomic neuropathy type 4
MONDO:0009745	neuronal ceroid lipofuscinosis 5
MONDO:0010734	spatial visualization, aptitude for
MONDO:0010733	hereditary spastic paraplegia 2
MONDO:0009744	neuronal ceroid lipofuscinosis 1
MONDO:0010736	split hand-foot malformation 2
MONDO:0009743	neurologic disease, infantile multisystem, with osseous fragility
MONDO:0009742	neuroectodermal melanolysosomal disease
MONDO:0010735	Kennedy disease
MONDO:0009741	neuroblastoma, susceptibility to
MONDO:0010738	spondylometaphyseal dysplasia, Golden type
MONDO:0009740	neurofaciodigitorenal syndrome
MONDO:0010737	spondyloepiphyseal dysplasia tarda, X-linked
MONDO:0010739	Taqi polymorphism
MONDO:0010741	tooth agenesis, selective, X-linked, 1
MONDO:0010740	taurodontism, microdontia, and dens invaginatus
MONDO:0010743	thrombocytopenia 1
MONDO:0010742	pentalogy of Cantrell
MONDO:0022712	oculo digital syndrome
MONDO:0022714	chester porphyria
MONDO:0022715	Chiari malformation type 3
MONDO:0022716	Chiari malformation type 4
MONDO:0009759	mosaic variegated aneuploidy syndrome 1
MONDO:0009758	congenital stationary night blindness 1B
MONDO:0009757	Niemann-Pick disease, type C1
MONDO:0009756	Niemann-Pick disease type A
MONDO:0010723	retinitis pigmentosa 2
MONDO:0010722	X-linked retinal dysplasia
MONDO:0009755	neutrophil actin dysfunction
MONDO:0010725	X-linked retinoschisis
MONDO:0009754	neutropenia, lethal congenital, with eosinophilia
MONDO:0009753	neurovisceral storage disease with Curvilinear bodies
MONDO:0010724	RP6
MONDO:0010727	Russell-silver syndrome, X-linked
MONDO:0009752	neuropathy, painful
MONDO:0010726	Rett syndrome
MONDO:0009751	neuropathy, hereditary sensory, atypical
MONDO:0009750	neuropathy, hereditary motor and sensory, with excessive myelin folding complex, autosomal recessive
MONDO:0010729	X-linked intellectual disability, Schimke type
MONDO:0010728	SCARF syndrome
MONDO:0010730	combined immunodeficiency, X-linked
MONDO:0010732	spastic paraparesis-deafness syndrome
MONDO:0010731	Simpson-Golabi-Behmel syndrome
MONDO:0022781	cleft lip palate-tetraphocomelia
MONDO:0022782	cleft lower lip cleft lateral canthi chorioretinal
MONDO:0019131	ossification anomalies-psychomotor developmental delay syndrome
MONDO:0019130	tubular renal disease-cardiomyopathy syndrome
MONDO:0022785	cleft palate cardiac defect ectrodactyly
MONDO:0022786	cleft palate colobomata radial synostosis deafness
MONDO:0022787	cleft palate heart disease polydactyly absent tibia
MONDO:0007148	appendicitis, proneness to
MONDO:0020126	rare peripheral neuropathy
MONDO:0007149	arbitrary restriction polymorphism 1
MONDO:0020125	acquired neuromuscular junction disease
MONDO:0010799	aminoglycoside-induced deafness
MONDO:0007146	apnea, central sleep
MONDO:0020124	neuromuscular junction disease
MONDO:0020123	metabolic myopathy
MONDO:0007147	obstructive sleep apnea syndrome
MONDO:0020122	acquired idiopathic inflammatory myopathy
MONDO:0007144	aortic arch interruption, facial palsy, and retinal coloboma
MONDO:0007145	aplasia cutis congenita
MONDO:0020121	muscular dystrophy
MONDO:0007142	Townes-Brocks syndrome
MONDO:0020120	skeletal muscle disease
MONDO:0007143	aortic arch anomaly-facial dysmorphism-intellectual disability syndrome
MONDO:0022780	cleft lip palate pituitary deficiency
MONDO:0007140	antiphospholipid syndrome
MONDO:0007141	antiviral state repressor, regulator of
MONDO:0020119	X-linked syndromic intellectual disability
MONDO:0020118	dense granule disease
MONDO:0020117	alpha granule disease
MONDO:0020116	rare blood coagulation disease
MONDO:0019137	non-24-hour sleep-wake syndrome
MONDO:0022778	cleft lip palate intellectual disability corneal opacity
MONDO:0019136	Zygomycosis
MONDO:0022779	cleft lip palate oligodontia syndactyly pili torti
MONDO:0019139	acquired hemophilia
MONDO:0019138	bleeding diathesis due to a collagen receptor defect
MONDO:0019133	visceral neuropathy-brain anomalies-facial dysmorphism-developmental delay syndrome
MONDO:0019132	spinal muscular atrophy-Dandy-Walker malformation-cataracts syndrome
MONDO:0019135	paracoccidioidomycosis
MONDO:0019134	central neurocytoma
MONDO:0022770	circumscribed cutaneous aplasia of the vertex
MONDO:0022771	circumscribed disseminated keratosis Jadassohn lew type
MONDO:0022772	classic Kaposi sarcoma
MONDO:0019120	pili bifurcati
MONDO:0022775	cleft lip and palate malrotation cardiopathy
MONDO:0022776	cleft lip and/or palate with mucous cysts of lower
MONDO:0022777	cleft lip palate dysmorphism kumar type
MONDO:0007159	arthrogryposis-like hand anomaly-sensorineural deafness syndrome
MONDO:0010789	MELAS syndrome
MONDO:0020115	secondary polycythemia
MONDO:0010788	Leber hereditary optic neuropathy
MONDO:0020114	polycythemia
MONDO:0020113	primary acquired red cell aplasia
MONDO:0007157	arthrogryposis, distal, type 1A
MONDO:0007158	arthrogryposis- oculomotor limitation-electroretinal anomalies syndrome
MONDO:0020112	vitamin B12- and folate-independent constitutional megaloblastic anemia
MONDO:0007155	arteritis, familial granulomatous, with juvenile polyarthritis
MONDO:0020111	constitutional megaloblastic anemia due to folate metabolism disorder
MONDO:0007156	arthritis, sacroiliac
MONDO:0020110	pulmonary agenesis
MONDO:0007153	arteries, anomalies of
MONDO:0007154	arteriovenous malformations of the brain
MONDO:0007151	arms, malformation of
MONDO:0010792	lethal infantile mitochondrial myopathy
MONDO:0007152	arrhythmogenic right ventricular dysplasia 1
MONDO:0010791	myoglobinuria, recurrent
MONDO:0010794	NARP syndrome
MONDO:0010793	nephropathy, chronic tubulointerstitial
MONDO:0020109	constitutional megaloblastic anemia due to vitamin B12 metabolism disorder
MONDO:0007150	arcus senilis
MONDO:0020108	autoimmune hemolytic anemia
MONDO:0010796	Parkinson disease, mitochondrial
MONDO:0020107	hemolytic anemia due to an erythrocyte nucleotide metabolism disorder
MONDO:0019129	global developmental delay-osteopenia-ectodermal defect syndrome
MONDO:0010795	oncocytic neoplasm
MONDO:0010798	proximal tubulopathy-diabetes mellitus-cerebellar ataxia syndrome
MONDO:0020106	hemolytic anemia due to a disorder of glycolytic enzymes
MONDO:0010797	Pearson syndrome
MONDO:0020105	hemolytic anemia due to hexose monophosphate shunt and glutathione metabolism anomalies
MONDO:0019126	intractable diarrhea of infancy
MONDO:0019125	relapsing polychondritis
MONDO:0022768	chronic polyradiculoneuritis
MONDO:0019128	mullerian aplasia
MONDO:0022769	ciliary dyskinesia-bronchiectasis
MONDO:0019127	polymyositis
MONDO:0019122	idiopathic acute eosinophilic pneumonia
MONDO:0019121	pneumocystosis
MONDO:0019124	microscopic polyangiitis
MONDO:0010790	MERRF syndrome
MONDO:0019123	continuous spikes and waves during sleep
MONDO:0022760	chromosome 22q deletion
MONDO:0022761	chromosome 3 duplication syndrome
MONDO:0022762	chromosome 4 short arm deletion
MONDO:0022765	chronic demyelinizing neuropathy with IgM monoclonal
MONDO:0007128	annular erythema
MONDO:0007129	tooth agenesis, selective, 1
MONDO:0007126	spondyloarthropathy, susceptibility to, 1
MONDO:0020104	rare constitutional hemolytic anemia due to an enzyme disorder
MONDO:0009789	nonarteritic anterior ischemic optic neuropathy, susceptibility to
MONDO:0010778	cyclic vomiting syndrome
MONDO:0007127	diffuse idiopathic skeletal hyperostosis
MONDO:0010777	cardiomyopathy, infantile hypertrophic
MONDO:0020103	constitutional hemolytic anemia due to acanthocytosis
MONDO:0009788	optic atrophy, hearing loss, and peripheral neuropathy, autosomal recessive
MONDO:0007124	ankyloblepharon-ectodermal defects-cleft lip/palate syndrome
MONDO:0009787	3-methylglutaconic aciduria type 3
MONDO:0020102	hereditary stomatocytosis
MONDO:0020101	constitutional hemolytic anemia due to membrane defect
MONDO:0009786	optic atrophy 6
MONDO:0010779	mitochondrial non-syndromic sensorineural deafness
MONDO:0007125	ankyloglossia
MONDO:0009785	opsismodysplasia
MONDO:0007122	anisocoria
MONDO:0020100	rare hemolytic anemia
MONDO:0007123	ankyloblepharon filiforme adnatum-cleft palate syndrome
MONDO:0009784	ophthalmoplegic neuromuscular disorder with abnormal mitochondria
MONDO:0007120	aniridia-absent patella syndrome
MONDO:0009783	progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 1
MONDO:0009782	ophthalmoplegia totalis with ptosis and miosis
MONDO:0007121	aniridia, microcornea, and spontaneously Reabsorbed cataract
MONDO:0009781	Onychotrichodysplasia and neutropenia
MONDO:0010781	ataxia and polyneuropathy, adult-onset
MONDO:0009780	lethal omphalocele-cleft palate syndrome
MONDO:0010780	mitochondrial myopathy with reversible cytochrome C oxidase deficiency
MONDO:0010783	Alzheimer disease, susceptibility to, mitochondrial
MONDO:0010782	myopathy, lactic acidosis, and sideroblastic anemia 3
MONDO:0019119	muscular channelopathy
MONDO:0010785	maternally-inherited diabetes and deafness
MONDO:0019118	inherited retinal dystrophy
MONDO:0010784	chloramphenicol toxicity
MONDO:0010787	Kearns-Sayre syndrome
MONDO:0010786	chronic diarrhea with villous atrophy
MONDO:0019115	obesity due to melanocortin 4 receptor deficiency
MONDO:0022756	chromosome 1q deletion
MONDO:0022757	chromosome 20 trisomy
MONDO:0019114	psychogenic movement disorders
MONDO:0019117	genetic nervous system disorder
MONDO:0022758	chromosome 22, monosome mosaic
MONDO:0019116	catecholamine-producing tumor
MONDO:0022759	trisomy 22
MONDO:0019111	familial thrombocytosis
MONDO:0019110	rare central nervous system or retinal vascular disease
MONDO:0019113	benign paroxysmal torticollis of infancy
MONDO:0019112	cancer-associated retinopathy
MONDO:0022752	chromosome 16p13.3 deletion syndrome
MONDO:0022754	chromosome 17p deletion
MONDO:0007139	Antipyrine metabolism
MONDO:0022755	chromosome 18 mosaic monosomy
MONDO:0007137	isolated congenital anosmia
MONDO:0010767	spermatogenic failure, Y-linked, 2
MONDO:0009799	pachydermoperiostosis
MONDO:0007138	anterior segment dysgenesis 1
MONDO:0010766	46,XX sex reversal 1
MONDO:0007135	nonsyndromic congenital nail disorder 6
MONDO:0010769	hairy ears, Y-linked
MONDO:0009798	intellectual disability-cataracts-calcified pinnae-myopathy syndrome
MONDO:0009797	orotic aciduria
MONDO:0010768	gonadoblastoma
MONDO:0007136	genetic anorectal anomalies
MONDO:0007133	anonychia-onychodystrophy with brachydactyly type b and ectrodactyly
MONDO:0009796	ornithine aminotransferase deficiency
MONDO:0007134	Cooks syndrome
MONDO:0009795	orofaciodigital syndrome IX
MONDO:0009794	orofaciodigital syndrome IV
MONDO:0007131	anonychia with flexural pigmentation
MONDO:0009793	orofaciodigital syndrome III
MONDO:0007132	anonychia-ectrodactyly
MONDO:0009792	ichthyosis-oral and digital anomalies syndrome
MONDO:0010770	ubiquitin-activating enzyme, Y-linked
MONDO:0007130	congenital total pulmonary venous return anomaly
MONDO:0009791	oral sensibility, disturbance of
MONDO:0010772	Leber optic atrophy and dystonia
MONDO:0009790	Opticocochleodentate degeneration
MONDO:0010771	histiocytoid cardiomyopathy
MONDO:0019108	silent sinus syndrome
MONDO:0010774	striatonigral degeneration, infantile, mitochondrial
MONDO:0019107	Rh deficiency syndrome
MONDO:0010773	myopathy and diabetes mellitus
MONDO:0010776	hypomagnesemia, hypertension, and hypercholesterolemia, mitochondrial
MONDO:0019109	CANOMAD syndrome
MONDO:0010775	retinitis pigmentosa-deafness syndrome
MONDO:0019104	Sandifer syndrome
MONDO:0022745	mixed dust pneumoconiosis
MONDO:0022746	chromosome 13p duplication
MONDO:0019103	benign exophthalmos syndrome
MONDO:0019106	disseminated peritoneal leiomyomatosis
MONDO:0019105	renal nutcracker syndrome
MONDO:0019100	neuromyelitis optica
MONDO:0022749	non-neoplastic nevus
MONDO:0019102	dentinogenesis imperfecta-short stature-hearing loss-intellectual disability syndrome
MONDO:0019101	retinal capillary malformation
MONDO:0009808	osteoid osteoma
MONDO:0009807	osteosarcoma
MONDO:0009806	Bruck syndrome 1
MONDO:0009805	osteogenesis imperfecta type 9
MONDO:0009804	osteogenesis imperfecta type 3
MONDO:0009803	congenital osteogenesis imperfecta-microcephaly-cataracts syndrome
MONDO:0009802	osteodysplasty, precocious, of Danks, Mayne, and Kozlowski
MONDO:0009801	familial osteodysplasia, Anderson type
MONDO:0009800	Blount disease, adolescent
MONDO:0009819	idiopathic juvenile osteoporosis
MONDO:0009818	autosomal recessive osteopetrosis 3
MONDO:0009817	autosomal recessive osteopetrosis 5
MONDO:0009816	autosomal recessive osteopetrosis 2
MONDO:0009815	autosomal recessive osteopetrosis 1
MONDO:0009814	osteopenia-intellectual disability-sparse hair syndrome
MONDO:0009813	chronic recurrent multifocal osteomyelitis
MONDO:0009812	osteomalacia, sclerosing, with cerebral calcification
MONDO:0009811	osteoma of middle ear
MONDO:0009810	autosomal recessive distal osteolysis syndrome
MONDO:0009809	multicentric osteolysis, nodulosis, and arthropathy
MONDO:0009849	hyperimmunoglobulinemia D with periodic fever
MONDO:0009848	dissecting cellulitis of the scalp
MONDO:0009847	pericardial effusion, chronic
MONDO:0022820	congenital articular rigidity
MONDO:0009846	pentosuria
MONDO:0009845	pelviscapular dysplasia
MONDO:0022821	congenital benign spinal muscular atrophy dominant
MONDO:0010833	Hirschsprung disease, susceptibility to, 2
MONDO:0009844	pellagra-like syndrome
MONDO:0009843	hypomyelinating leukodystrophy 3
MONDO:0010832	Bardet-Biedl syndrome 3
MONDO:0010835	pterygium colli-intellectual disability-digital anomalies syndrome
MONDO:0009842	Pelger-Huet-like anomaly and episodic fever with abdominal pain
MONDO:0010834	hirschsprung disease, susceptibility to, 5
MONDO:0009841	PEHO syndrome
MONDO:0010837	primary hyperparathyroidism
MONDO:0009840	Partington-Anderson syndrome
MONDO:0010836	nanophthalmos 1
MONDO:0010839	autosomal dominant congenital benign spinal muscular atrophy
MONDO:0010838	gonadal agenesis
MONDO:0022819	congenital arteriovenous shunt
MONDO:0010840	pachygyria-intellectual disability-epilepsy syndrome
MONDO:0010842	multiple cutaneous and mucosal venous malformations
MONDO:0010841	Waardenburg syndrome type 2B
MONDO:0022812	complement receptor deficiency
MONDO:0022815	congenital absence of the sternocleidomastoid muscle
MONDO:0022817	congenital amputation
MONDO:0022818	congenital aneurysms of the great vessels
MONDO:0010829	CARASIL syndrome
MONDO:0009859	PHAVER syndrome
MONDO:0009858	Pfeiffer-Palm-Teller syndrome
MONDO:0009857	persistent Mullerian duct syndrome
MONDO:0022810	Combarros Calleja Leno syndrome
MONDO:0009856	Peters plus syndrome
MONDO:0009855	d-bifunctional protein deficiency
MONDO:0010822	Warburg micro syndrome 1
MONDO:0010821	familial developmental dysphasia
MONDO:0009854	peroneus tertius muscle, absence of
MONDO:0009853	Imerslund-Grasbeck syndrome
MONDO:0010824	disorder of sex development-intellectual disability syndrome
MONDO:0009852	hereditary intrinsic factor deficiency
MONDO:0010823	rhizomelic chondrodysplasia punctata type 3
MONDO:0009851	peripheral neuropathy, ataxia, focal necrotizing encephalopathy, and spongy degeneration of brain
MONDO:0010826	childhood absence epilepsy
MONDO:0009850	periodontitis, chronic, adult
MONDO:0010825	atrioventricular defect-blepharophimosis-radial and anal defect syndrome
MONDO:0010828	retinitis pigmentosa 11
MONDO:0010827	retinitis pigmentosa 14
MONDO:0022809	Colver Steer Godman syndrome
MONDO:0010831	familial caudal dysgenesis
MONDO:0010830	neuronal ceroid lipofuscinosis 8
MONDO:0022800	type 2 collagenopathy
MONDO:0022802	Collins-Sakati syndrome
MONDO:0022803	coloboma porencephaly hydronephrosis
MONDO:0022804	colobomata unilobar lung heart defect
MONDO:0022805	colonic malakoplakia
MONDO:0010819	Stargardt disease 3
MONDO:0009829	pallidal degeneration, progressive, with retinitis pigmentosa
MONDO:0010818	retinitis pigmentosa 12
MONDO:0009828	palant cleft palate syndrome
MONDO:0009827	pachyonychia congenita, autosomal recessive
MONDO:0009826	PA polymorphism of alpha-2-globulin
MONDO:0009825	5-oxoprolinase deficiency
MONDO:0009824	primary hyperoxaluria type 2
MONDO:0009823	primary hyperoxaluria type 1
MONDO:0010811	benign prostatic hyperplasia
MONDO:0009822	otoonychoperoneal syndrome
MONDO:0010810	vitamin D hydroxylation-deficient rickets, type 1B
MONDO:0009821	lethal osteosclerotic bone dysplasia
MONDO:0010813	pancreatic beta cell agenesis with neonatal diabetes mellitus
MONDO:0009820	osteoporosis-pseudoglioma syndrome
MONDO:0010812	macrocytosis, familial
MONDO:0010815	spondyloepiphyseal dysplasia tarda with characteristic facies
MONDO:0010814	chondrodysplasia-pseudohermaphroditism syndrome
MONDO:0010817	autosomal dominant nonsyndromic deafness 2A
MONDO:0010816	Qazi Markouizos syndrome
MONDO:0010820	autosomal recessive juvenile Parkinson disease 2
MONDO:0010808	fatal familial insomnia
MONDO:0010807	autosomal recessive nonsyndromic deafness 2
MONDO:0009839	progressive supranuclear palsy-parkinsonism syndrome
MONDO:0010809	familial chronic myelocytic leukemia-like syndrome
MONDO:0009838	Parana hard-skin syndrome
MONDO:0009837	choroid plexus papilloma
MONDO:0009836	pancreatitis, sclerosing cholangitis, and sicca complex
MONDO:0009835	subacute sclerosing panencephalitis
MONDO:0009834	pancreatic insufficiency, combined exocrine
MONDO:0010800	Wolfram syndrome, mitochondrial form
MONDO:0009833	Shwachman-Diamond syndrome
MONDO:0009832	pancreatic agenesis
MONDO:0010802	pancreatic hypoplasia-diabetes-congenital heart disease syndrome
MONDO:0009831	malignant pancreatic neoplasm
MONDO:0009830	parkinsonian-pyramidal syndrome
MONDO:0010801	spondylocamptodactyly syndrome
MONDO:0010804	BRCATA
MONDO:0010803	Eiken syndrome
MONDO:0010806	retinitis pigmentosa 13
MONDO:0010805	bladder exstrophy
MONDO:0019052	inborn errors of metabolism
MONDO:0020041	46,XY disorder of sex development due to a defect in testosterone metabolism by peripheral tissue
MONDO:0019051	lysosomal disease
MONDO:0020040	46,XY disorder of sex development
MONDO:0019054	congenital limb malformation
MONDO:0019053	peroxisomal disease
MONDO:0019050	inherited hemoglobinopathy
MONDO:0020049	autosomal anomaly
MONDO:0020048	internal carotid agenesis
MONDO:0007069	Adie syndrome
MONDO:0020047	autosomal recessive syndromic cerebellar ataxia
MONDO:0020046	autosomal recessive degenerative and progressive cerebellar ataxia
MONDO:0020045	autosomal recessive cerebellar ataxia due to a DNA repair defect
MONDO:0007067	pyruvate kinase hyperactivity
MONDO:0007068	adenylosuccinate lyase deficiency
MONDO:0020044	autosomal recessive metabolic cerebellar ataxia
MONDO:0020043	autosomal recessive congenital cerebellar ataxia
MONDO:0044014	postpartum thyroiditis
MONDO:0007065	adenosine deaminase, elevated, hemolytic anemia due to
MONDO:0007066	adenosine triphosphatase deficiency, anemia due to
MONDO:0044013	puerperal disorder
MONDO:0020042	syndrome with 46,XY disorder of sex development
MONDO:0007063	long bone adamantinoma
MONDO:0007064	adenosine deaminase deficiency
MONDO:0007061	acylase, cobalt-activated
MONDO:0007062	congenital absence/hypoplasia of fingers excluding thumb, unilateral
MONDO:0007060	spermatogenic failure 6
MONDO:0020039	46,XX disorder of sex development induced by androgens excess
MONDO:0019059	rare parkinsonian disorder
MONDO:0019056	neuromuscular disease
MONDO:0019055	mitochondrial disease
MONDO:0019058	neurometabolic disease
MONDO:0019057	rare constitutional aplastic anemia
MONDO:0020030	rare genetic renal disease
MONDO:0019041	rare genetic inherited tumor
MONDO:0022693	cerebral calcification cerebellar hypoplasia
MONDO:0019040	chromosomal disorder
MONDO:0022694	cerebral calcifications opalescent teeth phosphaturia
MONDO:0019043	rare genetic skin disease
MONDO:0019042	multiple congenital anomalies/dysmorphic syndrome
MONDO:0022697	athetoid cerebral palsy
MONDO:0022699	cerebral palsy spastic hemiplegic
MONDO:0020038	gonadal dysgenesis of gynecological interest
MONDO:0020037	rare gynecological tumor
MONDO:0020036	rare nervous system tumor
MONDO:0020035	rare otorhinolaryngologic tumor
MONDO:0020034	rare respiratory tract neoplasm
MONDO:0007078	pseudohypoparathyroidism type 1A
MONDO:0007079	alcohol dependence
MONDO:0020033	rare digestive tumor
MONDO:0020032	rare urinary tract tumor
MONDO:0007076	ocular albinism with sensorineural deafness
MONDO:0022691	cerebello-olivary atrophy
MONDO:0020031	rare tumor
MONDO:0007077	Tietz syndrome
MONDO:0007074	ainhum
MONDO:0007075	alacrima, congenital, autosomal dominant
MONDO:0007072	ADULT syndrome
MONDO:0007073	hypoglossia-hypodactyly syndrome
MONDO:0007070	adiposis dolorosa
MONDO:0007071	adrenocortical hypofunction, chronic primary congenital
MONDO:0020029	rare genetic cardiac disease
MONDO:0020028	rare allergic respiratory disease
MONDO:0019049	rare dystonia
MONDO:0019048	rare vascular disease
MONDO:0019045	rare sleep disorder
MONDO:0019044	tumor of hematopoietic and lymphoid tissues
MONDO:0019047	rare deafness
MONDO:0019046	leukodystrophy
MONDO:0019030	Acanthamoeba keratitis
MONDO:0022682	cennamo gangemi syndrome
MONDO:0019032	X-linked intellectual disability with isolated growth hormone deficiency
MONDO:0019031	thrombocytopenia with congenital dyserythropoietic anemia
MONDO:0022685	cerebellar agenesis
MONDO:0022687	cerebellar degeneration
MONDO:0007049	acroleukopathy, symmetric
MONDO:0020027	rare allergic disease
MONDO:0020026	rare female infertility
MONDO:0044037	livedo reticularis
MONDO:0020025	rare male infertility
MONDO:0007047	punctate palmoplantar keratoderma type III
MONDO:0020024	rare infertility
MONDO:0007048	acrokeratosis verruciformis
MONDO:0007045	acrofacial dysostosis, Catania type
MONDO:0020023	respiratory or mediastinal malformation
MONDO:0007046	hereditary papulotranslucent acrokeratoderma
MONDO:0044033	posterior leukoencephalopathy syndrome
MONDO:0020022	central nervous system malformation
MONDO:0007043	Pfeiffer syndrome
MONDO:0020021	diaphragmatic or abdominal wall malformation
MONDO:0007044	acrodysostosis 1 with or without hormone resistance
MONDO:0020020	visceral malformation of the liver, biliary tract, pancreas or spleen
MONDO:0007041	apert syndrome
MONDO:0007042	Saethre-Chotzen syndrome
MONDO:0007040	Sakati-Nyhan syndrome
MONDO:0020019	digestive tract malformation
MONDO:0020018	cranial malformation
MONDO:0020017	rare otorhinolaryngologic disease
MONDO:0019038	rare maxillo-facial surgical disease
MONDO:0019037	progressive supranuclear palsy
MONDO:0019039	rare hemorrhagic disorder due to a constitutional coagulation factors defect
MONDO:0019034	accessory pancreas
MONDO:0019033	primary cutis verticis gyrata
MONDO:0019036	amoebiasis due to free-living amoebae
MONDO:0019035	pancreatoblastoma
MONDO:0022672	autosomal dominant cataract
MONDO:0019021	pigmented villonodular synovitis
MONDO:0022673	autosomal dominant non-nuclear cataract
MONDO:0019020	PANDAS
MONDO:0022675	cataract skeletal anomalies
MONDO:0022676	cataract - glaucoma
MONDO:0020016	rare neurologic disease with psychiatric involvement
MONDO:0010689	Charcot-Marie-Tooth disease X-linked recessive 4
MONDO:0020015	rare circulatory system disease
MONDO:0007058	acropectorovertebral dysplasia
MONDO:0020014	rare disease with odontological manifestation
MONDO:0007059	acrorenal syndrome
MONDO:0020013	rare odontologic disease
MONDO:0007056	acroosteolysis
MONDO:0020012	systemic or rheumatic disease
MONDO:0020011	rare headache disorder
MONDO:0007057	acroosteolysis dominant type
MONDO:0020010	infectious disease of the nervous system
MONDO:0007054	acromial dimples
MONDO:0007055	acromicric dysplasia
MONDO:0010693	nystagmus 1, congenital, X-linked
MONDO:0007052	growth hormone secreting pituitary adenoma 1
MONDO:0007053	restless legs syndrome 1
MONDO:0010692	nuclear ribonucleic acid
MONDO:0007050	acromegaloid changes, cutis verticis gyrata, and corneal leukoma
MONDO:0010695	occipital hair, white lock of
MONDO:0007051	acromegaloid facial appearance syndrome
MONDO:0010694	nystagmus, myoclonic
MONDO:0020009	rare neurologic disease
MONDO:0010697	ophthalmoplegia, external, and myopia
MONDO:0010696	omphalocele, X-linked
MONDO:0020008	rare immune disease
MONDO:0010699	Charcot-Marie-Tooth disease X-linked recessive 5
MONDO:0020007	absence of the pulmonary artery
MONDO:0010698	optic atrophy 2
MONDO:0020006	rare hematologic disease
MONDO:0019027	otopalatodigital syndrome
MONDO:0019026	autosomal recessive osteopetrosis
MONDO:0019029	segmental odontomaxillary dysplasia
MONDO:0019028	amoebiasis due to Entamoeba histolytica
MONDO:0019023	cutaneous mastocytosis
MONDO:0019022	sensorineural hearing loss-early graying-essential tremor syndrome
MONDO:0019025	extracutaneous mastocytoma
MONDO:0010691	Norrie disease
MONDO:0010690	congenital stationary night blindness 1A
MONDO:0019024	mast cell sarcoma
MONDO:0019096	rare pulmonary hypertension
MONDO:0020085	mastocytosis
MONDO:0019095	plague
MONDO:0020084	lymphoproliferative disease associated with primary immune disease
MONDO:0020083	immunodeficiency-associated lymphoproliferative disease
MONDO:0019098	autoimmune thrombocytopenia
MONDO:0020082	dendritic cell tumor
MONDO:0019097	hemorrhagic disorder due to a constitutional platelet anomaly
MONDO:0020081	macrophage or histiocytic tumor
MONDO:0019092	infantile apnea
MONDO:0019091	bronchopulmonary dysplasia
MONDO:0020080	histiocytic and dendritic cell tumor
MONDO:0019094	congenital Epstein-Barr virus infection
MONDO:0019093	immunodeficiency due to selective anti-polysaccharide antibody deficiency
MONDO:0019090	meconium aspiration syndrome
MONDO:0020089	acquired lipodystrophy
MONDO:0020088	familial partial lipodystrophy
MONDO:0020087	genetic lipodystrophy
MONDO:0020086	idiopathic interstitial pneumonia
MONDO:0019099	rare soft tissue tumor
MONDO:0020074	progressive myoclonus epilepsy
MONDO:0019085	vernal keratoconjunctivitis
MONDO:0020073	adolescent-onset epilepsy syndrome
MONDO:0019084	radiation proctitis
MONDO:0020072	childhood-onset epilepsy syndrome
MONDO:0019087	cholangiocarcinoma
MONDO:0020071	infantile epilepsy syndrome
MONDO:0019086	carcinoma of esophagus
MONDO:0020070	neonatal epilepsy syndrome
MONDO:0019081	alopecia universalis
MONDO:0019080	alopecia totalis
MONDO:0019083	Leigh syndrome with cardiomyopathy
MONDO:0019082	bullous pemphigoid
MONDO:0020079	plasma cell tumor
MONDO:0020078	acute myeloid leukemia with recurrent genetic anomaly
MONDO:0020077	myelodysplastic/myeloproliferative disease
MONDO:0020076	myeloproliferative neoplasm
MONDO:0020075	genetic non-syndromic obesity
MONDO:0019089	adult acute respiratory distress syndrome
MONDO:0019088	post-transplant lymphoproliferative disease
MONDO:0020063	malformation syndrome with hamartosis
MONDO:0019074	bilateral acute depigmentation of the iris
MONDO:0019073	hypotrichosis-lymphedema-telangiectasia-renal defect syndrome
MONDO:0020062	chromosome X structural anomaly
MONDO:0020061	chromosome Y structural anomaly
MONDO:0019076	circumscribed palmoplantar hypokeratosis
MONDO:0020060	gonosome structural anomaly
MONDO:0019075	Bosley-Salih-Alorainy syndrome
MONDO:0019070	liposarcoma
MONDO:0019072	intrahepatic cholestasis
MONDO:0019071	pure hair and nail ectodermal dysplasia
MONDO:0020069	chronic encephalitis
MONDO:0020068	postinfectious encephalitis
MONDO:0007089	Alzheimer disease 2
MONDO:0020067	infectious encephalitis
MONDO:0020066	Ehlers-Danlos syndrome
MONDO:0007087	alternating hemiplegia of childhood 1
MONDO:0020065	combined dystonia
MONDO:0007088	Alzheimer disease type 1
MONDO:0020064	pulmonary valve agenesis
MONDO:0007085	alopecia-epilepsy-pyorrhea-intellectual disability syndrome
MONDO:0007086	autosomal dominant Alport syndrome
MONDO:0007083	autosomal dominant palmoplantar keratoderma and congenital alopecia
MONDO:0007084	familial focal alopecia
MONDO:0007081	allergic bronchopulmonary aspergillosis
MONDO:0007082	alopecia areata 1
MONDO:0007080	glucocorticoid-remediable aldosteronism
MONDO:0019078	Ritscher-Schinzel syndrome
MONDO:0019077	warty dyskeratoma
MONDO:0019079	proximal spinal muscular atrophy
MONDO:0019063	vascular anomaly
MONDO:0020052	partial autosomal trisomy/tetrasomy
MONDO:0019062	rare infectious disease
MONDO:0020051	total autosomal trisomy
MONDO:0020050	autosomal trisomy
MONDO:0019065	amyloidosis
MONDO:0019064	hereditary spastic paraplegia
MONDO:0019061	rare parathyroid disease and phosphocalcic metabolism anomaly
MONDO:0019060	bone neoplasm
MONDO:0020059	gonosome number anomaly
MONDO:0020058	gonosome anomaly
MONDO:0020057	uniparental disomy of paternal origin
MONDO:0044001	hearing loss, mixed conductive-sensorineural
MONDO:0020056	uniparental disomy of maternal origin
MONDO:0020055	autosomal uniparental disomy
MONDO:0007098	ACys amyloidosis
MONDO:0020054	partial autosomal monosomy
MONDO:0007099	familial visceral amyloidosis
MONDO:0020053	total autosomal monosomy
MONDO:0007096	amenorrhea-galactorrhea syndrome
MONDO:0007097	Finnish type amyloidosis
MONDO:0007094	amelogenesis imperfecta type 1A
MONDO:0007095	ameloonychohypohidrotic syndrome
MONDO:0007092	amelogenesis imperfecta type 1B
MONDO:0007093	hypomaturation-hypoplastic amelogenesis imperfecta with taurodontism
MONDO:0007090	amastia, bilateral, with ureteral triplication and dysmorphism
MONDO:0007091	amelia and terminal transverse hemimelia
MONDO:0019067	idiopathic steroid-sensitive nephrotic syndrome
MONDO:0019066	syndrome with brachydactyly
MONDO:0019069	rhabdoid tumor
MONDO:0019068	congenital membranous nephropathy due to maternal anti-neutral endopeptidase alloimmunization
MONDO:0022620	CD4 deficiency
MONDO:0009649	moyamoya disease 1
MONDO:0009648	peripheral motor neuropathy-dysautonomia syndrome
MONDO:0022622	CDG syndrome type 4
MONDO:0009647	Morquio syndrome C
MONDO:0022623	CDK4 linked melanoma
MONDO:0009646	Monosomy 7 myelodysplasia and leukemia syndrome 1
MONDO:0010635	hypogonadotropic hypogonadism 1 with or without anosmia
MONDO:0009645	chronic mucocutaneous candidiasis due to monocyte chemotactic disorder
MONDO:0010634	jaundice, familial obstructive, of infancy
MONDO:0010637	keratosis follicularis spinulosa decalvans, X-linked
MONDO:0009644	sulfite oxidase deficiency due to molybdenum cofactor deficiency type B
MONDO:0009643	sulfite oxidase deficiency due to molybdenum cofactor deficiency type A
MONDO:0010636	Kallmann syndrome with spastic paraplegia
MONDO:0009642	orofaciodigital syndrome type II
MONDO:0010639	laryngeal abductor paralysis-intellectual disability syndrome
MONDO:0009641	mitochondrial complex II deficiency
MONDO:0010638	keratosis follicularis-dwarfism-cerebral atrophy syndrome
MONDO:0009640	mitochondrial complex I deficiency, nuclear type
MONDO:0010640	Leber optic atrophy, susceptibility to
MONDO:0010642	Lesch-Nyhan phenotype with normal HGPRT
MONDO:0010641	X-linked diffuse leiomyomatosis-Alport syndrome
MONDO:0010644	proteinuria, low molecular weight, with hypercalciuria and nephrocalcinosis
MONDO:0010643	acute leukemia
MONDO:0022613	bruyn scheltens syndrome
MONDO:0022615	burn goodship syndrome
MONDO:0022618	burning mouth syndrome type 3
MONDO:0022610	bronchiectasis oligospermia
MONDO:0009659	mucopolysaccharidosis type 4A
MONDO:0022611	Brunoni syndrome
MONDO:0022612	Brunsting-Perry syndrome
MONDO:0009658	Sanfilippo syndrome type D
MONDO:0009657	Sanfilippo syndrome type C
MONDO:0010624	IFAP/BRESHECK syndrome
MONDO:0009656	Sanfilippo syndrome type B
MONDO:0010623	ichthyosis and male hypogonadism
MONDO:0009655	Sanfilippo syndrome type A
MONDO:0010626	hyper-IgM syndrome type 1
MONDO:0009654	mucopolysaccharidoses, unclassified types
MONDO:0010625	immunodeficiency, X-linked, with deficiency of 115,000 Dalton surface glycoprotein
MONDO:0009653	mucolipidosis type IV
MONDO:0010628	immunoglobulin M, level of
MONDO:0010627	X-linked lymphoproliferative syndrome
MONDO:0009652	mucolipidosis type III gamma
MONDO:0009651	pseudo-Hurler polydystrophy
MONDO:0009650	mucolipidosis type II
MONDO:0010629	impacted teeth, multiple
MONDO:0010631	incontinentia pigmenti
MONDO:0010630	imprinting gene related to retinoblastoma
MONDO:0010633	iris hypoplasia with glaucoma
MONDO:0010632	developmental and epileptic encephalopathy, 1
MONDO:0022602	brachydactyly small stature face anomalies
MONDO:0022603	brachydactyly tibial hypoplasia
MONDO:0022605	brachymetapody anodontia hypotrichosis albinoidism
MONDO:0022606	branchial arch disease
MONDO:0022607	extraovarian Brenner tumor of the vagina
MONDO:0022608	brittle bone syndrome lethal type
MONDO:0022609	bronchial adenomas/carcinoids childhood
MONDO:0009629	Desbuquois dysplasia 1
MONDO:0009628	microcolon
MONDO:0009627	Galloway-Mowat syndrome
MONDO:0009626	pseudo-TORCH syndrome
MONDO:0009625	diencephalic-mesencephalic junction dysplasia syndrome 1
MONDO:0009624	microcephaly and chorioretinopathy 1
MONDO:0010613	inborn glycerol kinase deficiency
MONDO:0010612	hydrocephaly-cerebellar agenesis syndrome
MONDO:0009623	Nijmegen breakage syndrome
MONDO:0010615	isolated growth hormone deficiency type III
MONDO:0009622	Jawad syndrome
MONDO:0010614	X-linked congenital generalized hypertrichosis
MONDO:0009621	microcephaly-cervical spine fusion anomalies syndrome
MONDO:0009620	Say-Barber-Miller syndrome
MONDO:0010617	male hypergonadotropic hypogonadism-intellectual disability-skeletal anomalies syndrome
MONDO:0010616	hypogonadism, male
MONDO:0010619	X-linked dominant hypophosphatemic rickets
MONDO:0010618	familial isolated hypoparathyroidism due to agenesis of parathyroid gland
MONDO:0010620	hypouricemia, familial renal, due to tubular hypersecretion
MONDO:0010622	recessive X-linked ichthyosis
MONDO:0010621	CHILD syndrome
MONDO:0010609	Hirschsprung disease with type d brachydactyly
MONDO:0009639	mitochondrial myopathy with lactic acidosis
MONDO:0009638	mitochondrial myopathy with a defect in mitochondrial-protein transport
MONDO:0009637	inborn mitochondrial myopathy
MONDO:0009636	mitochondrial DNA depletion syndrome 3
MONDO:0010602	hemophilia A
MONDO:0009635	microvillus inclusion disease
MONDO:0010601	gynecomastia, familial
MONDO:0009634	microtia with meatal atresia and conductive deafness
MONDO:0009633	microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma
MONDO:0010604	hemophilia B
MONDO:0010603	hemophilia A with vascular abnormality
MONDO:0009632	microphthalmia with hyperopia, retinal degeneration, macrophakia, and dental anomalies
MONDO:0009631	isolated microphthalmia 1
MONDO:0010606	hernia, anterior diaphragmatic
MONDO:0009630	microphthalmia, isolated, with coloboma 4
MONDO:0010605	hemopoietic proliferation
MONDO:0010608	Hhhh syndrome
MONDO:0010607	heterotaxy, visceral, 1, X-linked
MONDO:0010611	X-linked hydrocephalus with stenosis of the aqueduct of Sylvius
MONDO:0010610	holoprosencephaly-hypokinesia-congenital contractures syndrome
MONDO:0019010	congenital isolated hyperinsulinism
MONDO:0022662	carpo tarsal osteolysis recessive
MONDO:0007029	branchio-oto-renal syndrome
MONDO:0022666	cassavism
MONDO:0020005	rare endocrine disease
MONDO:0007027	non-alcoholic steatohepatitis
MONDO:0010679	Duchenne muscular dystrophy
MONDO:0020004	rare eye disease
MONDO:0009689	congenital myasthenic syndrome 6
MONDO:0007028	rotator cuff syndrome
MONDO:0010678	muscular dystrophy, progressive Pectorodorsal
MONDO:0009688	myasthenia gravis
MONDO:0020003	rare surgical cardiac disease
MONDO:0007025	chancre
MONDO:0009687	myasthenia, congenital, refractory to acetylcholinesterase inhibitors
MONDO:0020002	rare surgical thoracic disease
MONDO:0007026	non-alcoholic fatty liver
MONDO:0009686	musk, inability to smell
MONDO:0007023	Yersinia infectious disease
MONDO:0020001	respiratory or thoracic malformation
MONDO:0007024	Yersinia pseudotuberculosis infectious disease
MONDO:0009685	Miyoshi myopathy
MONDO:0020000	rare respiratory disease
MONDO:0007021	wheat allergic disease
MONDO:0009684	muscular hypertonia, lethal
MONDO:0009683	autosomal recessive limb-girdle muscular dystrophy type 2H
MONDO:0007022	xanthogranulomatous pyelonephritis
MONDO:0010682	myoclonic epilepsy, progressive, X-linked
MONDO:0009682	muscular dystrophy, congenital, with rapid progression
MONDO:0007020	Wernicke encephalopathy
MONDO:0009681	Ullrich congenital muscular dystrophy 1
MONDO:0010681	myelolymphatic insufficiency
MONDO:0009680	congenital muscular dystrophy-infantile cataract-hypogonadism syndrome
MONDO:0010684	X-linked myopathy with excessive autophagy
MONDO:0010683	X-linked centronuclear myopathy
MONDO:0010686	N syndrome
MONDO:0010685	myopia 1, X-linked
MONDO:0019019	osteogenesis imperfecta
MONDO:0010688	hereditary sensory neuropathy X-linked
MONDO:0010687	nephrolithiasis, X-linked recessive, with renal failure
MONDO:0019016	maternally-inherited progressive external ophthalmoplegia
MONDO:0019015	omphalocele
MONDO:0019018	Tako-tsubo cardiomyopathy
MONDO:0019017	short fifth metacarpals-insulin resistance syndrome
MONDO:0019012	Carpenter syndrome
MONDO:0019011	Charcot-Marie-Tooth disease type 1
MONDO:0010680	X-linked Emery-Dreifuss muscular dystrophy
MONDO:0019014	mutilating palmoplantar keratoderma with periorificial keratotic plaques
MONDO:0019013	non-histaminic angioedema
MONDO:0022650	cardiomyopathy diabetes deafness
MONDO:0022651	cardiomyopathy dilated with conduction defect type 1
MONDO:0022652	cardiomyopathy dilated with conduction defect type 2
MONDO:0022653	cardiomyopathy due to anthracyclines
MONDO:0022654	cardiomyopathy hypogonadism collagenoma syndrome
MONDO:0022655	cardiomyopathy hypogonadism metabolic anomalies
MONDO:0022656	cardiomyopathy spherocytosis
MONDO:0010668	skeletal dysplasia-intellectual disability syndrome
MONDO:0007038	Achoo syndrome
MONDO:0007039	neurofibromatosis type 2
MONDO:0010667	Prieto syndrome
MONDO:0009699	action myoclonus-renal failure syndrome
MONDO:0007036	Achard syndrome
MONDO:0009698	Unverricht-Lundborg syndrome
MONDO:0007037	achondroplasia
MONDO:0010669	syndactyly type 8
MONDO:0009697	Lafora disease
MONDO:0007034	Adams-Oliver syndrome
MONDO:0007035	acanthosis nigricans
MONDO:0009696	juvenile myoclonic epilepsy
MONDO:0007032	prune belly syndrome
MONDO:0009695	myeloproliferative disease, autosomal recessive
MONDO:0009694	myeloperoxidase deficiency
MONDO:0007033	abducens nerve palsy
MONDO:0009693	plasma cell myeloma
MONDO:0007030	autosomal dominant Aarskog syndrome
MONDO:0010671	microphthalmia, syndromic 1
MONDO:0009692	primary myelofibrosis
MONDO:0007031	familial abdominal aortic aneurysm
MONDO:0010670	X-linked intellectual disability-spastic quadriparesis syndrome
MONDO:0009691	mycosis fungoides
MONDO:0010673	modifier, X-linked, for Neurofunctional defects
MONDO:0009690	congenital myasthenic syndrome 10
MONDO:0010672	linear skin defects with multiple congenital anomalies
MONDO:0019009	isolated focal cortical dysplasia
MONDO:0010675	muscular dystrophy, cardiac type
MONDO:0010674	mucopolysaccharidosis type 2
MONDO:0019008	benign recurrent intrahepatic cholestasis
MONDO:0010677	muscular dystrophy, Mabry type
MONDO:0010676	muscular dystrophy, Hemizygous lethal type
MONDO:0022646	cardiofacial syndrome short limbs
MONDO:0019005	nephronophthisis
MONDO:0019004	kidney Wilms tumor
MONDO:0022647	cardiomelic syndrome stratton Koehler type
MONDO:0022648	cardiomyopathy and deafness due to tRNA lysine gene mutation
MONDO:0019007	vaginal atresia
MONDO:0019006	familial idiopathic steroid-resistant nephrotic syndrome
MONDO:0019001	biotin-responsive basal ganglia disease
MONDO:0019000	perineural cyst
MONDO:0019003	multiple endocrine neoplasia type 2
MONDO:0019002	Lhermitte-Duclos disease
MONDO:0022642	childhood carcinoid tumor
MONDO:0007009	ureterolithiasis
MONDO:0022643	carcinoma of the vocal tract
MONDO:0007007	Ureaplasma urethritis
MONDO:0022644	cardiac hydatid cysts with intracavitary expansion
MONDO:0009669	spinal muscular atrophy, type 1
MONDO:0007008	uremia
MONDO:0022645	cardioencephalomyopathy
MONDO:0010657	methylmalonic acidemia with homocystinuria, type cblX
MONDO:0009668	lethal multiple pterygium syndrome
MONDO:0007005	ulcerative proctosigmoiditis
MONDO:0010656	intellectual disability, X-linked 1
MONDO:0009667	muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A3
MONDO:0007006	ulnar neuropathy
MONDO:0009666	holocarboxylase synthetase deficiency
MONDO:0010659	FRAXE intellectual disability
MONDO:0007003	twin-to-twin transfusion syndrome
MONDO:0009665	biotinidase deficiency
MONDO:0010658	syndromic X-linked intellectual disability 12
MONDO:0007004	type III hypersensitivity disease
MONDO:0007001	tricuspid valve prolapse
MONDO:0009664	mulibrey nanism
MONDO:0007002	trochlear nerve disease
MONDO:0009663	mucus inspissation of respiratory tract
MONDO:0009662	mucopolysaccharidosis type 7
MONDO:0009661	mucopolysaccharidosis type 6
MONDO:0007000	Treponema infectious disease
MONDO:0009660	mucopolysaccharidosis type 4B
MONDO:0010660	intellectual disability, X-linked 9
MONDO:0010662	paraplegia-intellectual disability-hyperkeratosis syndrome
MONDO:0010661	severe X-linked intellectual disability, Gustavson type
MONDO:0010664	syndromic X-linked intellectual disability Snyder type
MONDO:0010663	X-linked intellectual disability-hypotonic face syndrome
MONDO:0010666	Miles-Carpenter syndrome
MONDO:0010665	Wilson-Turner syndrome
MONDO:0022636	candida glabrata infection
MONDO:0022639	Cantu sanchez-corona Garcia-Cruz syndrome
MONDO:0022633	camptodactyly joint contractures and facial skeletal dysplasia
MONDO:0007018	vulvitis
MONDO:0007019	vulvovaginitis
MONDO:0022634	camptodactyly vertebral fusion
MONDO:0007016	vitamin A deficiency
MONDO:0009679	arthrogryposis due to muscular dystrophy
MONDO:0010646	macular dystrophy, X-linked
MONDO:0009678	muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4
MONDO:0010645	oculocerebrorenal syndrome
MONDO:0007017	vitreous detachment
MONDO:0009677	autosomal recessive limb-girdle muscular dystrophy type 2C
MONDO:0007014	vibrio infectious disease
MONDO:0010648	major affective disorder 2
MONDO:0007015	viral meningitis
MONDO:0009676	autosomal recessive limb-girdle muscular dystrophy type 2B
MONDO:0010647	spermatogenic failure, X-linked, 2
MONDO:0009675	autosomal recessive limb-girdle muscular dystrophy type 2A
MONDO:0007012	variant Creutzfeldt-Jakob disease
MONDO:0009674	muscular dystrophy, adult-onset, with leukoencephalopathy
MONDO:0007013	vasculogenic impotence
MONDO:0010649	isolated congenital megalocornea
MONDO:0009673	spinal muscular atrophy, type II
MONDO:0007010	uveitis
MONDO:0009672	spinal muscular atrophy, type III
MONDO:0007011	uveoparotid fever
MONDO:0009671	intellectual disability-myopathy-short stature-endocrine defect syndrome
MONDO:0009670	lethal congenital contracture syndrome 1
MONDO:0010651	Menkes disease
MONDO:0010650	Melnick-Needles syndrome
MONDO:0010653	Renpenning syndrome
MONDO:0010652	X-linked intellectual disability-seizures-psoriasis syndrome
MONDO:0010655	X-linked intellectual disability with marfanoid habitus
MONDO:0010654	Partington syndrome
MONDO:0010719	radiation sensitivity of natural killer activity
MONDO:0009729	nephropathy - deafness - hyperparathyroidism syndrome
MONDO:0009728	nephronophthisis 1
MONDO:0009727	atelosteogenesis type II
MONDO:0009726	proteosome-associated autoinflammatory syndrome
MONDO:0009725	nemaline myopathy 2
MONDO:0009724	nail-patella-like renal disease
MONDO:0022700	cerebral palsy spastic monoplegic
MONDO:0009723	Leigh syndrome
MONDO:0010712	panhypopituitarism, X-linked
MONDO:0010711	TARP syndrome
MONDO:0009722	Bailey-Bloch congenital myopathy
MONDO:0009721	Nathalie syndrome
MONDO:0010714	Pelizaeus-Merzbacher disease
MONDO:0010713	properdin deficiency, X-linked
MONDO:0009720	Keipert syndrome
MONDO:0010716	X-linked lethal multiple pterygium syndrome
MONDO:0010715	pseudohermaphroditism, incomplete male, type 1
MONDO:0010718	absent radius-anogenital anomalies syndrome
MONDO:0010717	pyruvate dehydrogenase E1-alpha deficiency
MONDO:0010721	reticuloendotheliosis, X-linked
MONDO:0010720	partial androgen insensitivity syndrome
MONDO:0010709	early-onset parkinsonism-intellectual disability syndrome
MONDO:0010708	Pallister-W syndrome
MONDO:0009739	infantile neuroaxonal dystrophy
MONDO:0009738	sialidosis type 2
MONDO:0009737	galactosialidosis
MONDO:0009736	Neu-Laxova syndrome 1
MONDO:0009735	Netherton syndrome
MONDO:0009734	hyperinsulinemic hypoglycemia, familial, 1
MONDO:0010701	opticoacoustic nerve atrophy with dementia
MONDO:0010700	optic atrophy--spastic paraplegia syndrome
MONDO:0009733	nephrotic syndrome, type 4
MONDO:0010703	ornithine carbamoyltransferase deficiency
MONDO:0009732	congenital nephrotic syndrome, Finnish type
MONDO:0010702	orofaciodigital syndrome I
MONDO:0009731	nephrosis-deafness-urinary tract-digital malformations syndrome
MONDO:0010705	ouabain resistance
MONDO:0009730	nephrosialidosis
MONDO:0010704	otopalatodigital syndrome type 1
MONDO:0010707	Paine syndrome
MONDO:0010706	premature ovarian failure 1
MONDO:0010710	Pierre Robin syndrome-faciodigital anomaly syndrome
MONDO:0009709	myopathy, centronuclear, 2
MONDO:0009708	myopathy, myosin storage, autosomal recessive
MONDO:0009707	myopathy with giant abnormal mitochondria
MONDO:0009706	hereditary myopathy with lactic acidosis due to ISCU deficiency
MONDO:0009705	carnitine palmitoyl transferase 1A deficiency
MONDO:0009704	carnitine palmitoyl transferase II deficiency, myopathic form
MONDO:0009703	myopathy with abnormal lipid metabolism
MONDO:0009702	myopathy due to malate-aspartate shuttle defect
MONDO:0009701	myopathy, granulovacuolar lobular, with electrical myotonia
MONDO:0009700	Carey-Fineman-Ziter syndrome
MONDO:0009719	familial atrial myxoma
MONDO:0009718	myxedema
MONDO:0009717	Schwartz-Jampel syndrome
MONDO:0009716	Richieri Costa-da Silva syndrome
MONDO:0009715	myotonia congenita, autosomal recessive
MONDO:0009714	myosclerosis
MONDO:0009713	myopia 18, autosomal recessive
MONDO:0009712	congenital multicore myopathy with external ophthalmoplegia
MONDO:0009711	congenital fiber-type disproportion myopathy
MONDO:0009710	myotonia congenita
MONDO:0044098	ovarian ectopic pregnancy
MONDO:0044092	collagenous sprue
MONDO:0020096	autosomal recessive isolated diffuse palmoplantar keratoderma
MONDO:0020095	autosomal dominant disease associated with focal palmoplantar keratoderma as a major feature
MONDO:0020094	autosomal dominant disease with diffuse palmoplantar keratoderma as a major feature
MONDO:0020093	autosomal dominant isolated diffuse palmoplantar keratoderma
MONDO:0020092	rare idiopathic male infertility
MONDO:0020091	male infertility due to obstructive azoospermia
MONDO:0020090	male infertility due to gonadal dysgenesis
MONDO:0020099	inherited sideroblastic anemia
MONDO:0020098	constitutional anemia due to iron metabolism disorder
MONDO:0020097	autosomal recessive disease with focal palmoplantar keratoderma as a major feature
MONDO:0044067	candidiasis, invasive
MONDO:0044070	candidemia
MONDO:0044079	cardio-renal syndrome
MONDO:0044083	alternariosis
MONDO:0015490	predominantly small-vessel vasculitis
MONDO:0015499	paralytic facial malformation
MONDO:0015494	isolated dystonia
MONDO:0015493	lipoatrophy with diabetes, leukomelanodermic papules, liver steatosis, and hypertrophic cardiomyopathy
MONDO:0015492	Anti-neutrophil cytoplasmic antibody-associated vasculitis
MONDO:0015491	immune complex mediated vasculitis
MONDO:0015498	oromandibular-limb anomalies syndrome
MONDO:0015497	hypoglossia/aglossia
MONDO:0015496	macroglossia
MONDO:0015495	otomandibular dysplasia associated with monogenic syndromes
MONDO:0027462	autosomal recessive cutis laxa type 2C
MONDO:0015489	predominantly medium-vessel vasculitis
MONDO:0015488	predominantly large-vessel vasculitis
MONDO:0015483	mandibulofacial dysostosis
MONDO:0015482	otomandibular dysplasia
MONDO:0015481	coloboma of inferior eyelid
MONDO:0015480	coloboma of superior eyelid
MONDO:0015487	fatal infantile encephalocardiomyopathy
MONDO:0015486	keratoconus
MONDO:0015485	primary hereditary glaucoma
MONDO:0015484	cysticercosis
MONDO:0003487	pseudoglandular squamous cell carcinoma
MONDO:0003488	anal squamous cell carcinoma
MONDO:0003489	middle ear squamous cell carcinoma
MONDO:0003483	gastric squamous cell carcinoma
MONDO:0027451	autosomal recessive cutis laxa type 2D
MONDO:0003484	penis squamous cell carcinoma
MONDO:0003485	colon squamous cell carcinoma
MONDO:0003486	basaloid squamous cell carcinoma
MONDO:0003480	pineal region dysgerminoma
MONDO:0003481	dysgerminoma of ovary
MONDO:0003482	Pediculus humanus corporis infestation
MONDO:0015479	submucosal cleft palate
MONDO:0015478	paramedian facial cleft
MONDO:0015477	pinnae fistula or cyst
MONDO:0015472	cryptococcosis
MONDO:0015471	benign focal seizures of adolescence
MONDO:0015470	familial isolated dilated cardiomyopathy
MONDO:0015476	cysts and fistulae of the face and oral cavity
MONDO:0015475	rare head and neck malformation
MONDO:0015474	cryptosporidiosis
MONDO:0015473	cryptorchidism-arachnodactyly-intellectual disability syndrome
MONDO:0003498	gallbladder squamous cell carcinoma
MONDO:0003499	sarcomatoid squamous cell skin carcinoma
MONDO:0003494	ovarian squamous cell carcinoma
MONDO:0003495	ovarian squamous cell neoplasm
MONDO:0003496	endometrial squamous cell carcinoma
MONDO:0003497	renal pelvis squamous cell carcinoma
MONDO:0003490	ampulla of vater squamous cell carcinoma
MONDO:0003491	rectum squamous cell carcinoma
MONDO:0003492	lacrimal gland squamous cell carcinoma
MONDO:0003493	thymus squamous cell carcinoma
MONDO:0015469	craniosynostosis
MONDO:0015468	craniosynostosis-cataract syndrome
MONDO:0015467	craniosynostosis, Philadelphia type
MONDO:0015466	cranio-osteoarthropathy
MONDO:0015461	short rib-polydactyly syndrome
MONDO:0015460	adrenocortical carcinoma
MONDO:0015465	craniometaphyseal dysplasia
MONDO:0015464	craniofrontonasal dysplasia-Poland anomaly syndrome
MONDO:0015463	craniodigital syndrome-intellectual disability syndrome
MONDO:0015462	thin ribs-tubular bones-dysmorphism syndrome
MONDO:0003425	ophthalmoplegia
MONDO:0003426	clear cell adenoma
MONDO:0003427	bronchus adenoma
MONDO:0003428	brain hemangioma
MONDO:0003421	mixed cell adenoma
MONDO:0003422	lung adenoma
MONDO:0003423	middle ear adenoma
MONDO:0003424	oncocytic adenoma
MONDO:0015409	isolated congenital syngnathia
MONDO:0003420	bile duct cystadenoma
MONDO:0015408	diffuse lymphatic malformation
MONDO:0015414	paramedian nasal cleft
MONDO:0015413	median cleft of the upper lip and maxilla
MONDO:0015412	median facial cleft
MONDO:0015411	facial cleft
MONDO:0015418	lateral facial cleft
MONDO:0015417	Tessier number 6 facial cleft
MONDO:0015416	Tessier number 5 facial cleft
MONDO:0015415	oblique facial cleft
MONDO:0015410	nasal dorsum fistula/cyst
MONDO:0003418	bile duct adenoma
MONDO:0003419	Bartholin gland adenoma
MONDO:0003436	lung oat cell carcinoma
MONDO:0003437	occult small cell lung carcinoma
MONDO:0003438	combined small cell lung carcinoma
MONDO:0003439	urinary bladder villous adenoma
MONDO:0003432	strabismus
MONDO:0003433	water-clear cell adenoma
MONDO:0003434	vaginal adenoma
MONDO:0003435	microcystic adenoma
MONDO:0003430	prolactin producing pituitary tumor
MONDO:0003431	lipoadenoma
MONDO:0015403	non-involuting congenital hemangioma
MONDO:0015402	mandibular arteriovenous malformation
MONDO:0015401	maxillary arteriovenous malformation
MONDO:0015400	frontonasal arteriovenous malformation
MONDO:0015407	cerebrofacial arteriovenous metameric syndrome type 3
MONDO:0015406	cerebrofacial arteriovenous metameric syndrome type 1
MONDO:0015405	cerebrofacial arteriovenous metameric syndrome
MONDO:0015404	rapidly involuting congenital hemangioma
MONDO:0003429	functioning pituitary gland adenoma
MONDO:0003403	testicular non-seminomatous germ cell cancer
MONDO:0003404	adult yolk sac tumor
MONDO:0003405	adult central nervous system germ cell tumor
MONDO:0003406	sleep-wake disorder
MONDO:0003400	childhood endodermal sinus tumor
MONDO:0003401	central nervous system endodermal sinus tumor
MONDO:0003402	testicular yolk sac tumor
MONDO:0003414	skin pilomatrix carcinoma
MONDO:0003415	hemoglobin d disease
MONDO:0003416	hemoglobin E disease
MONDO:0003417	internuclear ophthalmoplegia
MONDO:0003410	Wolffian duct adenocarcinoma
MONDO:0003411	breast hemangiopericytoma
MONDO:0003412	retroperitoneal hemangiopericytoma
MONDO:0003413	hair follicle neoplasm
MONDO:0003407	ovarian yolk sac tumor
MONDO:0003408	ovarian primitive germ cell tumor
MONDO:0003409	colonic disease
MONDO:0003469	epithelioid cell synovial sarcoma
MONDO:0003465	fibrous synovial sarcoma
MONDO:0003466	spindle cell synovial sarcoma
MONDO:0003467	mediastinum synovial sarcoma
MONDO:0003468	biphasic synovial sarcoma
MONDO:0003461	fallopian tube serous adenofibroma
MONDO:0003462	papillary adenofibroma
MONDO:0003463	ovarian endometrioid adenofibroma
MONDO:0003464	cystadenofibroma
MONDO:0003460	clear cell adenofibroma
MONDO:0015458	intellectual disability-hypoplastic corpus callosum-preauricular tag syndrome
MONDO:0015457	corpus callosum agenesis-double urinary collecting system syndrome
MONDO:0015456	whooping cough
MONDO:0015455	gonococcal conjunctivitis
MONDO:0015459	nasopharyngeal carcinoma
MONDO:0015450	triatrial heart
MONDO:0015454	multiple carboxylase deficiency
MONDO:0015453	Cogan syndrome
MONDO:0015452	Coffin-Siris syndrome
MONDO:0015451	univentricular heart
MONDO:0003476	clear cell ependymoma
MONDO:0003477	brain stem ependymoma
MONDO:0003478	childhood ependymoma
MONDO:0003479	toxic pneumonitis
MONDO:0003472	lice infestation
MONDO:0003473	spinal cord ependymoma
MONDO:0003474	tanycytic ependymoma
MONDO:0003475	papillary ependymoma
MONDO:0003470	cellular ependymoma
MONDO:0003471	Pediculus humanus capitis infestation
MONDO:0015447	differentiated thyroid carcinoma
MONDO:0015446	atypical coarctation of aorta
MONDO:0015445	autosomal dominant coarctation of aorta
MONDO:0015444	cleidocranial dysplasia
MONDO:0015449	criss-cross heart
MONDO:0015448	mitochondrial complex III deficiency
MONDO:0015443	chromosome 8-derived supernumerary ring/marker
MONDO:0015442	hereditary breast and ovarian cancer syndrome
MONDO:0015441	ring chromosome 7
MONDO:0015440	ring chromosome 6
MONDO:0003447	clear cell hidradenoma
MONDO:0003448	benign spiradenoma
MONDO:0003449	syringocystadenoma papilliferum
MONDO:0003443	papillary urothelial neoplasm
MONDO:0003444	intrahepatic bile duct adenoma
MONDO:0003445	extrahepatic bile duct adenoma
MONDO:0027416	retinal cone dystrophy 2
MONDO:0003446	papillary hidradenoma
MONDO:0003440	bladder flat intraepithelial lesion
MONDO:0003441	dystonic disorder
MONDO:0003442	bladder papillary urothelial neoplasm
MONDO:0015436	ring chromosome 20
MONDO:0015435	ring chromosome 19
MONDO:0015434	ring chromosome 18
MONDO:0015433	ring chromosome 17
MONDO:0015439	ring chromosome 4
MONDO:0015438	ring chromosome 22
MONDO:0015437	ring chromosome 21
MONDO:0015432	ring chromosome 12
MONDO:0015431	ring chromosome 10
MONDO:0015430	ring chromosome 1
MONDO:0003458	uterine corpus adenofibroma
MONDO:0003459	cervical adenofibroma
MONDO:0027407	Kleefstra syndrome 1
MONDO:0003454	conjunctival cancer
MONDO:0003455	bile duct papillary neoplasm
MONDO:0003456	bile duct mucinous cystic neoplasm
MONDO:0003457	ovarian serous adenofibroma
MONDO:0003450	eccrine papillary adenoma
MONDO:0003451	laryngeal neuroendocrine tumor
MONDO:0003452	cochlear disease
MONDO:0003453	conjunctival intraepithelial neoplasm
MONDO:0015419	midline cervical cleft
MONDO:0015425	lethal recessive chondrodysplasia
MONDO:0015424	lethal chondrodysplasia, Moerman type
MONDO:0015423	anaplastic thyroid carcinoma
MONDO:0015422	orofaciodigital syndrome type 13
MONDO:0015429	choroideremia-hypopituitarism syndrome
MONDO:0015428	choroidal atrophy-alopecia syndrome
MONDO:0015427	paroxysmal dyskinesia
MONDO:0015426	Desbuquois dysplasia
MONDO:0015421	orofaciodigital syndrome type 12
MONDO:0015420	cleft lip and alveolus
MONDO:0005923	Pneumocystis infectious disease
MONDO:0005922	pleural tuberculosis
MONDO:0005925	pneumonic pasteurellosis
MONDO:0005924	pneumocystosis
MONDO:0005921	Plasmodium vivax malaria
MONDO:0005920	Plasmodium falciparum malaria
MONDO:0017909	inherited glutathione synthetase deficiency
MONDO:0017905	X-linked mendelian susceptibility to mycobacterial diseases
MONDO:0017906	amyloidosis cutis dyschromia
MONDO:0017907	primary lymphoma of the conjunctiva
MONDO:0017908	hyperekplexia
MONDO:0017912	X-linked pure spastic paraplegia
MONDO:0017913	pure or complex hereditary spastic paraplegia
MONDO:0017914	pure or complex autosomal dominant spastic paraplegia
MONDO:0017915	pure or complex autosomal recessive spastic paraplegia
MONDO:0017910	dehydrated hereditary stomatocytosis
MONDO:0017911	cleft lip/palate-ectodermal dysplasia syndrome
MONDO:0005919	placental insufficiency
MONDO:0005916	placenta accreta
MONDO:0005915	pityriasis versicolor
MONDO:0005918	placenta praevia
MONDO:0005917	placenta disease
MONDO:0005934	pyruvate decarboxylase deficiency
MONDO:0005933	pulmonary blastoma
MONDO:0005936	recurrent pneumonia
MONDO:0005935	reactive arthritis
MONDO:0005930	postpoliomyelitis syndrome
MONDO:0005932	pseudorabies
MONDO:0005931	progressive multifocal leukoencephalopathy
MONDO:0017901	autosomal recessive mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency
MONDO:0017902	autosomal recessive mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR2 deficiency
MONDO:0017903	autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR2 deficiency
MONDO:0017904	steroid dehydrogenase deficiency-dental anomalies syndrome
MONDO:0017900	autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete IFNgammaR2 deficiency
MONDO:0005927	polyomavirus infectious disease
MONDO:0005926	poliomyelitis
MONDO:0005929	postpartum depression
MONDO:0005928	post-thrombotic syndrome
MONDO:0005901	pasteurellosis
MONDO:0005900	parotitis
MONDO:0005903	pericardial tuberculosis
MONDO:0005902	peanut allergic reaction
MONDO:0005912	phencyclidine abuse
MONDO:0005911	pharyngoconjunctival fever
MONDO:0005914	Picornaviridae infectious disease
MONDO:0005913	phlebotomus fever
MONDO:0005910	phagocyte bactericidal dysfunction
MONDO:0005909	pestivirus infectious disease
MONDO:0005908	peste des petits ruminants infectious disease
MONDO:0005905	periodic limb movement disorder
MONDO:0005904	pericarditis
MONDO:0005907	persian gulf syndrome
MONDO:0005906	peritonsillar abscess
MONDO:0003388	ampulla of vater clear cell adenocarcinoma
MONDO:0003389	epithelial-myoepithelial carcinoma
MONDO:0003384	uterine ligament clear cell adenocarcinoma
MONDO:0003385	cervical clear cell adenocarcinoma
MONDO:0003386	bladder clear cell adenocarcinoma
MONDO:0003387	urethra clear cell adenocarcinoma
MONDO:0003380	endometrial clear cell adenocarcinoma
MONDO:0003381	pituitary gland disease
MONDO:0003382	eyelid disease
MONDO:0027353	autosomal recessive dyskeratosis congenita 4
MONDO:0003383	fallopian tube clear cell adenocarcinoma
MONDO:0015379	cervical dermoid cyst
MONDO:0015378	fourth branchial cleft anomaly
MONDO:0015373	Saldino-Mainzer syndrome
MONDO:0015372	autosomal dominant macrothrombocytopenia
MONDO:0015371	linear atrophoderma of Moulin
MONDO:0015377	third branchial cleft anomaly
MONDO:0015376	first branchial cleft anomaly
MONDO:0015375	orofaciodigital syndrome
MONDO:0015374	primary central nervous system vasculitis
MONDO:0003399	pineal region yolk sac tumor
MONDO:0003395	testicular granulosa cell tumor
MONDO:0003396	epulis
MONDO:0003397	gingival hypertrophy
MONDO:0003398	anterograde amnesia
MONDO:0003391	vulvar alveolar soft part sarcoma
MONDO:0003392	fallopian tube germ cell tumor
MONDO:0003393	thymus gland disease
MONDO:0003394	dental pulp disease
MONDO:0015369	Joubert syndrome and related disorders
MONDO:0015368	neuro-ophthalmological disease
MONDO:0003390	glycogen-rich clear cell breast carcinoma
MONDO:0015367	Charlie M syndrome
MONDO:0015362	autosomal dominant distal hereditary motor neuropathy
MONDO:0015361	autosomal recessive hereditary demyelinating motor and sensory neuropathy
MONDO:0015360	autosomal dominant hereditary axonal motor and sensory neuropathy
MONDO:0015366	autosomal recessive hereditary sensory and autonomic neuropathy
MONDO:0015365	autosomal dominant hereditary sensory and autonomic neuropathy
MONDO:0015364	hereditary sensory and autonomic neuropathy
MONDO:0015363	autosomal recessive distal hereditary motor neuropathy
MONDO:0003366	hydrarthrosis
MONDO:0003367	gastric leiomyosarcoma
MONDO:0003368	prostate leiomyosarcoma
MONDO:0003369	vagina leiomyosarcoma
MONDO:0003362	cutaneous leiomyosarcoma
MONDO:0003363	malignant dermis tumor
MONDO:0003364	gallbladder leiomyosarcoma
MONDO:0003365	esophagus leiomyosarcoma
MONDO:0003360	small intestine leiomyosarcoma
MONDO:0003361	small intestinal sarcoma
MONDO:0015359	autosomal dominant hereditary demyelinating motor and sensory neuropathy
MONDO:0015358	hereditary motor and sensory neuropathy
MONDO:0015357	secondary hypoparathyroidism due to impaired parathormon secretion
MONDO:0015356	hereditary neoplastic syndrome
MONDO:0015351	neuropathy with hearing impairment
MONDO:0015350	17q11.2 microduplication syndrome
MONDO:0015355	distal hereditary motor neuropathy type 7
MONDO:0015354	hereditary sensory and autonomic neuropathy with deafness and global delay
MONDO:0015353	neuronopathy, distal hereditary motor, type 5A
MONDO:0015352	distal hereditary motor neuropathy type 2
MONDO:0003377	extrahepatic bile duct leiomyosarcoma
MONDO:0003378	liver leiomyosarcoma
MONDO:0003379	rectum leiomyosarcoma
MONDO:0003373	kidney leiomyosarcoma
MONDO:0003374	laryngeal leiomyosarcoma
MONDO:0003375	uterus leiomyosarcoma
MONDO:0003376	mediastinum leiomyosarcoma
MONDO:0003370	retroperitoneal leiomyosarcoma
MONDO:0003371	breast leiomyosarcoma
MONDO:0003372	vulvar leiomyosarcoma
MONDO:0015348	leukoencephalopathy with bilateral anterior temporal lobe cysts
MONDO:0015347	multicentric reticulohistiocytosis
MONDO:0015346	Jeavons syndrome
MONDO:0015345	perioral myoclonia with absences
MONDO:0015349	progressive cavitating leukoencephalopathy
MONDO:0015340	drug rash with eosinophilia and systemic symptoms
MONDO:0015344	idiopathic acute transverse myelitis
MONDO:0015343	secondary acute transverse myelitis
MONDO:0015342	acute transverse myelitis
MONDO:0015341	congenital panfollicular nevus
MONDO:0030967	deafness, congenital, and adult-onset progressive leukoencephalopathy
MONDO:0030966	neurofacioskeletal syndrome with or without renal agenesis
MONDO:0030963	Li-Campeau syndrome
MONDO:0030962	nephrotic syndrome, type 23
MONDO:0030965	olmsted syndrome 2
MONDO:0030971	immunodeficiency 78 with autoimmunity and developmental delay
MONDO:0030978	endove syndrome, limb-only type
MONDO:0030977	neuropathy, hereditary motor, with myopathic features
MONDO:0030979	endove syndrome, limb-brain type
MONDO:0030974	mitochondrial complex 2 deficiency, nuclear type 4
MONDO:0030973	immunodeficiency 77
MONDO:0030976	oculomotor-abducens synkinesis
MONDO:0042960	Sackey-Sakati-Aur syndrome
MONDO:0042961	sacral hemangiomas multiple congenital abnormalities
MONDO:0042962	Slti-Salem syndrome
MONDO:0042956	Saal-Bulas syndrome
MONDO:0030981	immunodeficiency 79
MONDO:0030982	sulfide quinone oxidoreductase deficiency
MONDO:0030989	spermatogenic failure 53
MONDO:0030988	developmental delay with dysmorphic facies and dental anomalies
MONDO:0015391	nasopharyngeal teratoma
MONDO:0030985	premature ovarian failure 19
MONDO:0015390	proboscis lateralis
MONDO:0030987	vertebral, cardiac, tracheoesophageal, renal, and limb defects
MONDO:0030986	blistering, acantholytic, of oral and laryngeal mucosa
MONDO:0042970	disorder of glutamate decarboxylase
MONDO:0042971	congenital herpes virus infection
MONDO:0042972	meningococcemia
MONDO:0042973	familial osteosclerosis
MONDO:0042967	rheumatic disease of mitral valve
MONDO:0042968	partial duplication of chromosome 12
MONDO:0042969	partial duplication of the long arm of chromosome 12
MONDO:0042963	wandering spleen
MONDO:0042964	Machado-Joseph disease type 4
MONDO:0042965	Machado-Joseph disease type 5
MONDO:0042966	inherited mitral valve disease
MONDO:0015395	congenital subglottic stenosis
MONDO:0030992	short stature, oligodontia, dysmorphic facies, and motor delay
MONDO:0015394	nasal encephalocele
MONDO:0030991	bile acid conjugation defect 1
MONDO:0030994	neurodevelopmental disorder with or without autism or seizures
MONDO:0015393	nasal ganglioglioma
MONDO:0015392	nasal glial heterotopia
MONDO:0015399	glossopalatine ankylosis
MONDO:0015398	hemifacial microsomia
MONDO:0015397	oculo-auriculo-vertebral spectrum
MONDO:0030990	Kohlschutter-Tonz syndrome-like
MONDO:0015396	congenital laryngeal cyst
MONDO:0030999	neurodevelopmental disorder with cerebral atrophy and variable facial dysmorphism
MONDO:0030996	bleeding disorder, platelet-type, 24
MONDO:0015380	facial dermoid cyst
MONDO:0030995	global developmental delay with speech and behavioral abnormalities
MONDO:0030998	deafness, autosomal dominant 80
MONDO:0030997	mitochondrial complex 1 deficiency, nuclear type 37
MONDO:0042981	aortic valve stenosis
MONDO:0042982	GATA2 deficiency with susceptibility to MDS/AML
MONDO:0042983	neurocutaneous syndrome
MONDO:0042980	Westphal disease
MONDO:0042979	hypokalemic periodic paralysis, type 1
MONDO:0015389	supernumerary nostril
MONDO:0042974	parainfluenza virus type 3 infectious disease
MONDO:0042975	pseudoachondroplastic dysplasia 2
MONDO:0042976	vitamin B deficiency
MONDO:0042977	trichoepithelioma, multiple familial, 1
MONDO:0015384	digestive duplication cyst of the tongue
MONDO:0015383	cervicofacial fibrochondroma
MONDO:0015382	lower lip fistula
MONDO:0015381	commissural lip fistula
MONDO:0015388	polyrrhinia
MONDO:0015387	nasolacrimal duct cyst
MONDO:0015386	epignathus
MONDO:0015385	external auditory canal aplasia/hypoplasia
MONDO:0003304	plexiform neurofibroma
MONDO:0005967	splenic tuberculosis
MONDO:0030923	frontotemporal dementia and/or amyotrophic lateral sclerosis
MONDO:0005966	spleen cancer
MONDO:0030922	intellectual disability, autosomal dominant 56
MONDO:0003305	cellular neurofibroma
MONDO:0005969	st. Louis encephalitis
MONDO:0003306	atypical neurofibroma
MONDO:0030925	oocyte maturation defect 10
MONDO:0005968	sporotrichosis
MONDO:0003307	multiple mucosal neuroma
MONDO:0030924	proteasome-associated autoinflammatory syndrome 5
MONDO:0003300	appendix leiomyoma
MONDO:0005963	sparganosis
MONDO:0003301	dartoic leiomyoma
MONDO:0005962	skeletal tuberculosis
MONDO:0003302	epithelioid neurofibroma
MONDO:0030921	intellectual disability, autosomal dominant 55, with seizures
MONDO:0005965	spinal stenosis
MONDO:0003303	neurofibroma of gallbladder
MONDO:0005964	sphenoid sinusitis
MONDO:0030920	intellectual disability, autosomal dominant 54
MONDO:0005961	sinusitis
MONDO:0005960	silicosis
MONDO:0030927	myofibrillar myopathy 11
MONDO:0017949	ABeta amyloidosis, Arctic type
MONDO:0030926	spermatogenic failure 51
MONDO:0030929	microcephaly 27, primary, autosomal dominant
MONDO:0030928	microcephaly 26, primary, autosomal dominant
MONDO:0017956	mixed autoinflammatory and autoimmune syndrome
MONDO:0017957	unclassified autoinflammatory syndrome
MONDO:0042902	Say-Carpenter syndrome
MONDO:0017958	magic syndrome
MONDO:0017959	JMP syndrome
MONDO:0017952	non-familial rare disease with dilated cardiomyopathy
MONDO:0017953	hereditary periodic fever syndrome
MONDO:0017954	pyogenic autoinflammatory syndrome
MONDO:0017955	granulomatous autoinflammatory syndrome
MONDO:0017950	microcephalic primordial dwarfism
MONDO:0017951	trichorhinophalangeal syndrome
MONDO:0005959	sick building syndrome
MONDO:0042908	Schaap-Taylor-Baraitser syndrome
MONDO:0005978	theileriasis
MONDO:0003315	endometrium carcinoma in situ
MONDO:0030934	intellectual developmental disorder, autosomal dominant 64
MONDO:0005977	tabes dorsalis
MONDO:0003316	nonanaplastic kidney Wilms tumor
MONDO:0030933	Joubert syndrome 37
MONDO:0030936	epilepsy, progressive myoclonic, 12
MONDO:0003317	metachronous kidney Wilms' tumor
MONDO:0003318	mixed cell type kidney Wilms' tumor
MONDO:0030935	mitochondrial complex 2 deficiency, nuclear type 2
MONDO:0005979	thoracic outlet syndrome
MONDO:0005974	strongyloidiasis
MONDO:0003311	endometrial stromal tumor
MONDO:0030930	neurodevelopmental disorder with or without early-onset generalized epilepsy
MONDO:0003312	ovarian endometrioid stromal and related neoplasms
MONDO:0005973	Strongylida infectious disease
MONDO:0003313	endometrioid stromal sarcoma of the vagina
MONDO:0005976	syphilis
MONDO:0003314	endometrioid stromal and related neoplasms of the vagina
MONDO:0005975	suppurative otitis media
MONDO:0030931	proteasome-associated autoinflammatory syndrome 4
MONDO:0005970	staphylococcal pneumonia
MONDO:0005972	streptococcal pneumonia
MONDO:0005971	staphyloenterotoxemia
MONDO:0003310	Monckeberg arteriosclerosis
MONDO:0030938	spermatogenic failure 52
MONDO:0017938	X-linked cleft palate and ankyloglossia
MONDO:0030937	mitochondrial complex 2 deficiency, nuclear type 3
MONDO:0017939	classic multiminicore myopathy
MONDO:0030939	premature ovarian failure 18
MONDO:0017945	ABetaL34V amyloidosis
MONDO:0042912	Schlegelberger-Grote syndrome
MONDO:0042913	Schrander-stumpel-Theunissen-Hulsmans syndrome
MONDO:0017946	ABeta amyloidosis, Iowa type
MONDO:0017947	ABeta amyloidosis, Italian type
MONDO:0017948	ABetaA21G amyloidosis
MONDO:0042915	Schmitt-Gillenwater-Kelly syndrome
MONDO:0017941	chikungunya
MONDO:0017942	Hendra virus infection
MONDO:0017943	autoerythrocyte sensitization syndrome
MONDO:0017944	invasive non-typhoidal salmonellosis
MONDO:0042911	Schwartz-Cohen-addad-Lambert syndrome
MONDO:0017940	autosomal dominant Charcot-Marie-Tooth disease type 2 due to KIF5A mutation
MONDO:0003308	pleural mesothelioma
MONDO:0003309	pleural cancer
MONDO:0005945	rhinoscleroma
MONDO:0005944	Rhabdoviridae infectious disease
MONDO:0030947	neurodegeneration, childhood-onset, with hypotonia, respiratory insufficiency, and brain imaging abnormalities
MONDO:0005947	rickettsial pneumonia
MONDO:0005946	rhinosporidiosis
MONDO:0005941	retroperitoneal cancer
MONDO:0030941	erythrokeratodermia variabilis et progressiva 7
MONDO:0005940	respirovirus infectious disease
MONDO:0005943	Rhabditida infectious disease
MONDO:0005942	Reye syndrome
MONDO:0017927	severe lateral tibial bowing with short stature
MONDO:0017928	9p13 microdeletion syndrome
MONDO:0017929	congenital achiasma
MONDO:0017934	aphonia-deafness-retinal dystrophy-bifid halluces-intellectual disability syndrome
MONDO:0017935	hyperinsulinism due to HNF1A deficiency
MONDO:0042924	Vagneur-Triolle-Ripert syndrome
MONDO:0017936	benign Samaritan congenital myopathy
MONDO:0017937	autosomal dominant intermediate Charcot-Marie-Tooth disease with neuropathic pain
MONDO:0017930	mixed sclerosing bone dystrophy with extra-skeletal manifestations
MONDO:0017931	hereditary inclusion body myopathy type 4
MONDO:0017932	muscular hypertrophy-hepatomegaly-polyhydramnios syndrome
MONDO:0017933	hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial DNA mutation
MONDO:0005938	renal tuberculosis
MONDO:0005937	REM sleep behavior disorder
MONDO:0005939	Reoviridae infectious disease
MONDO:0005956	septicemic plague
MONDO:0005955	scrub typhus
MONDO:0005958	sex cord-stromal tumor
MONDO:0005957	setariasis
MONDO:0005952	scarlet fever
MONDO:0005951	sarcocystosis
MONDO:0005954	screw worm infectious disease
MONDO:0030953	short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies 2
MONDO:0005953	scirrhous adenocarcinoma
MONDO:0005950	Salmonella gastroenteritis
MONDO:0017916	pure or complex X-linked spastic paraplegia
MONDO:0017917	maternally-inherited spastic paraplegia
MONDO:0017918	white matter hypoplasia-corpus callosum agenesis-intellectual disability syndrome
MONDO:0017919	bladder exstrophy-epispadias-cloacal exstrophy complex
MONDO:0017923	multiple synostoses syndrome
MONDO:0017924	central nervous system calcification-deafness-tubular acidosis-anemia syndrome
MONDO:0017925	T-cell immunodeficiency with epidermodysplasia verruciformis
MONDO:0017926	multiple paragangliomas associated with polycythemia
MONDO:0017920	deafness-genital anomalies-metacarpal and metatarsal synostosis syndrome
MONDO:0017921	hearing loss-familial salivary gland insensitivity to aldosterone syndrome
MONDO:0017922	deafness-onychodystrophy syndrome
MONDO:0030961	Olmsted syndrome 2
MONDO:0005949	roseolovirus infectious disease
MONDO:0005948	Ritter disease
MONDO:0003348	conventional leiomyosarcoma
MONDO:0003349	central nervous system leiomyosarcoma
MONDO:0003344	hemangioblastoma
MONDO:0003345	hilar cholangiocarcinoma
MONDO:0003346	central nervous system vasculitis
MONDO:0003347	inflammatory leiomyosarcoma
MONDO:0003340	malignant glomus tumor
MONDO:0003341	subungual glomus tumor
MONDO:0003342	benign perivascular tumor
MONDO:0003343	retinal hemangioblastoma
MONDO:0015337	isolated craniosynostosis
MONDO:0015336	malformation syndrome with odontal and/or periodontal component
MONDO:0015335	orofacial clefting syndrome
MONDO:0015334	branchial arch or oral-acral syndrome
MONDO:0017996	blepharophimosis - intellectual disability syndrome due to UBE3B deficiency
MONDO:0017997	telecanthus-hypertelorism-strabismus-pes cavus syndrome
MONDO:0017998	PLA2G6-associated neurodegeneration
MONDO:0015339	adrenomyeloneuropathy
MONDO:0015338	syndromic craniosynostosis
MONDO:0017999	fatty acid hydroxylase-associated neurodegeneration
MONDO:0017992	autoinflammatory syndrome with pyogenic bacterial infection and amylopectinosis
MONDO:0017993	cerebral sinovenous thrombosis
MONDO:0017994	severe early-onset obesity-insulin resistance syndrome due to SH2B1 deficiency
MONDO:0017995	spondylocostal dysostosis-hypospadias-intellectual disability syndrome
MONDO:0015333	progeroid syndrome
MONDO:0015332	rare developmental defect with connective tissue involvement
MONDO:0017990	catecholaminergic polymorphic ventricular tachycardia
MONDO:0015331	malformation syndrome with skin/mucosae involvement
MONDO:0017991	Takayasu arteritis
MONDO:0015330	overgrowth/obesity syndrome
MONDO:0003359	myxoid leiomyosarcoma
MONDO:0003355	ovary leiomyosarcoma
MONDO:0003356	epithelioid leiomyosarcoma
MONDO:0003357	lung leiomyosarcoma
MONDO:0003358	anus leiomyosarcoma
MONDO:0003351	colon leiomyosarcoma
MONDO:0003352	colon sarcoma
MONDO:0003353	heart leiomyosarcoma
MONDO:0003354	heart sarcoma
MONDO:0003350	granular cell leiomyosarcoma
MONDO:0015326	night blindness-skeletal anomalies-dysmorphism syndrome
MONDO:0017989	His bundle tachycardia
MONDO:0015325	cataract-deafness-hypogonadism syndrome
MONDO:0015324	cataract-intellectual disability-anal atresia-urinary defects syndrome
MONDO:0015323	teratogenic Pierre Robin syndrome
MONDO:0017985	congenital radioulnar synostosis
MONDO:0015329	malformation syndrome with short stature
MONDO:0017986	disorder of plasmalogens biosynthesis
MONDO:0015328	rare bone development disorder
MONDO:0017987	syringomyelia
MONDO:0015327	developmental anomaly of metabolic origin
MONDO:0017988	multifocal atrial tachycardia
MONDO:0017981	syngnathia-cleft palate syndrome
MONDO:0017982	humeroradial synostosis
MONDO:0017983	humero-radio-ulnar synostosis
MONDO:0017984	familial lambdoid synostosis
MONDO:0015322	Pierre Robin syndrome associated with bone disease
MONDO:0015321	Pierre Robin syndrome associated with branchial archs anomalies
MONDO:0015320	Pierre Robin syndrome associated with a chromosomal anomaly
MONDO:0017980	syngnathia multiple anomalies
MONDO:0005989	toxoplasmosis
MONDO:0003326	intermixed schwannian stroma-rich ganglioneuroblastoma
MONDO:0003327	peripheral ganglioneuroblastoma
MONDO:0005988	toxocariasis
MONDO:0030900	intellectual developmental disorder with paroxysmal dyskinesia or seizures
MONDO:0003328	fallopian tube adenomatoid tumor
MONDO:0030903	Hermansky-Pudlak syndrome 11
MONDO:0030902	mitochondrial complex 1 deficiency, nuclear type 36
MONDO:0003329	ureteral obstruction
MONDO:0005985	Togaviridae infectious disease
MONDO:0003322	epithelial predominant Wilms' tumor
MONDO:0005984	tinea pedis
MONDO:0005987	toxascariasis
MONDO:0003324	stromal predominant kidney Wilms' tumor
MONDO:0005986	torovirus infectious disease
MONDO:0003325	nodular ganglioneuroblastoma
MONDO:0030909	intellectual disability, X-linked, syndromic, Houge type
MONDO:0005981	tick paralysis
MONDO:0005980	tick infestation
MONDO:0030908	intellectual disability, X-linked, syndromic, 35
MONDO:0005983	tinea favosa
MONDO:0003320	blastema predominant kidney Wilms tumor
MONDO:0005982	tinea infection
MONDO:0003321	hereditary Wilms tumor
MONDO:0015309	Auriculocondylar syndrome
MONDO:0030905	deafness, autosomal recessive 117
MONDO:0030907	intellectual disability, X-linked 106
MONDO:0030906	Trichomonas tenax infectious disease
MONDO:0017978	syndrome with disorder of sex development of gynecological interest
MONDO:0015315	neonatal brainstem dysfunction
MONDO:0015314	primary laryngeal lymphangioma
MONDO:0017979	autoimmune lymphoproliferative syndrome
MONDO:0015313	choanal atresia, bilateral
MONDO:0015312	choanal atresia, unilateral
MONDO:0015319	rare disease with Pierre Robin syndrome
MONDO:0017974	46,XY disorder of sex development induced by maternal-exposure to endocrine disruptors
MONDO:0015318	Pierre Robin syndrome associated with collagen disease
MONDO:0017975	sex chromosome disorder of sex development
MONDO:0015317	laryngotracheal angioma
MONDO:0017976	disorder of sex development of gynecological interest
MONDO:0015316	congenital laryngeal palsy
MONDO:0017977	46,XY disorder of sex development of gynecological interest
MONDO:0017970	46,XY disorder of sex development due to impaired androgen production
MONDO:0017971	46,XY disorder of sex development due to a cholesterol synthesis defect
MONDO:0017972	classic congenital lipoid adrenal hyperplasia due to STAR deficency
MONDO:0017973	non-classic congenital lipoid adrenal hyperplasia due to STAR deficency
MONDO:0015311	autism-facial port-wine stain syndrome
MONDO:0003319	scrotum neoplasm
MONDO:0015310	syndromic optic nerve hypoplasia
MONDO:0003337	acute hemorrhagic encephalitis
MONDO:0030912	intellectual disability, autosomal dominant 47
MONDO:0005999	tuberculous empyema
MONDO:0030911	intellectual disability, autosomal dominant 46
MONDO:0003338	von Economo disease
MONDO:0030914	Clark-Baraitser syndrome
MONDO:0003339	hepatoerythropoietic porphyria
MONDO:0030913	intellectual disability, autosomal dominant 48
MONDO:0005996	trichuriasis
MONDO:0003333	benign struma ovarii
MONDO:0005995	trichostrongylosis
MONDO:0003334	demyelinating polyneuropathy
MONDO:0030910	intellectual disability, autosomal dominant 45
MONDO:0003335	chronic polyneuropathy
MONDO:0005998	trombiculiasis
MONDO:0003336	acute necrotizing encephalitis
MONDO:0005997	tricuspid valve stenosis
MONDO:0005992	trichinosis
MONDO:0030919	intellectual disability, autosomal dominant 53
MONDO:0005991	trench fever
MONDO:0003330	urinary tract obstruction
MONDO:0003331	ovarian monodermal teratoma
MONDO:0005994	trichostrongyloidiasis
MONDO:0005993	Trichomonas vaginitis urogenital infection
MONDO:0003332	malignant struma ovarii
MONDO:0030916	intellectual disability, autosomal dominant 50
MONDO:0030915	intellectual disability, autosomal recessive 61
MONDO:0005990	tracheitis
MONDO:0030918	intellectual disability, autosomal dominant 52
MONDO:0030917	intellectual disability, autosomal dominant 51
MONDO:0015304	arachnoiditis
MONDO:0017967	testicular agenesis
MONDO:0017968	46,XY ovotesticular disorder of sex development
MONDO:0015303	macular amyloidosis
MONDO:0015302	nodular cutaneous amyloidosis
MONDO:0017969	46,XY disorder of sex development of endocrine origin
MONDO:0015301	primary cutaneous amyloidosis
MONDO:0015308	laminopathy type Decaudain-Vigouroux
MONDO:0017963	46,XX disorder of sex development induced by endogenous maternal-derived androgen
MONDO:0015307	Madras motor neuron disease
MONDO:0017964	46,XX disorder of sex development induced by exogenous maternal-derived androgen
MONDO:0015306	Lemierre syndrome
MONDO:0017965	syndrome with 46,XX disorder of sex development
MONDO:0017966	46,XY disorder of gonadal development
MONDO:0015305	rare endometriosis
MONDO:0017960	CANDLE syndrome
MONDO:0017961	46,XX disorder of gonadal development
MONDO:0017962	46,XX disorder of sex development induced by fetoplacental androgens excess
MONDO:0015300	cataract - microcornea syndrome
MONDO:0005802	hymenolepiasis
MONDO:0005801	human T-lymphotropic virus 1 infectious disease
MONDO:0005804	hyperprolactinemia
MONDO:0005803	hyperinsulinemic hypoglycemia
MONDO:0005800	hordeolum
MONDO:0005813	interdigitating dendritic cell sarcoma
MONDO:0005812	influenza
MONDO:0005815	pancreatic neuroendocrine neoplasm
MONDO:0005814	intestinal cancer
MONDO:0005811	infectious myxomatosis
MONDO:0005810	infectious mononucleosis
MONDO:0005809	infectious ectromelia
MONDO:0005806	hypopharynx cancer
MONDO:0005805	hypodermyiasis
MONDO:0005808	inclusion conjunctivitis
MONDO:0005807	idiopathic CD4-positive T-lymphocytopenia
MONDO:0500018	acute fibrinous and organizing pneumonia
MONDO:0500000	episodic angioedema with eosinophilia
MONDO:0015193	hydrops fetalis
MONDO:0015192	unclassified intestinal pseudoobstruction
MONDO:0015191	myopathic intestinal pseudoobstruction
MONDO:0015190	leiomyosarcoma of small intestine
MONDO:0015197	aneurysm of sinus of Valsalva
MONDO:0015196	vein of Galen aneurysm
MONDO:0015195	atresia of urethra
MONDO:0015194	sideroblastic anemia
MONDO:0015199	aniridia - intellectual disability syndrome
MONDO:0015198	aniridia-ptosis-intellectual disability-familial obesity syndrome
MONDO:0015182	congenital enteropathy involving intestinal mucosa development
MONDO:0015181	congenital intestinal disease due to an enzymatic defect
MONDO:0015180	intestinal disease due to fat malabsorption
MONDO:0015186	rare tumor of intestine
MONDO:0015185	intestinal polyposis syndrome
MONDO:0015184	rare disease involving intestinal motility
MONDO:0015183	short bowel syndrome
MONDO:0015189	adenocarcinoma of small instestine
MONDO:0015188	metabolic disease with intestinal involvement
MONDO:0015187	rare inflammatory bowel disease
MONDO:0054782	leukodystrophy, hypomyelinating, 15
MONDO:0054781	combined oxidative phosphorylation deficiency 36
MONDO:0054780	elliptocytosis 3
MONDO:0054785	multiple mitochondrial dysfunctions syndrome 6
MONDO:0054771	keratoconus 9
MONDO:0054770	orofaciodigital syndrome 18
MONDO:0054776	epilepsy, familial focal, with variable foci 4
MONDO:0054794	hydrocephalus, congenital, 3, with brain anomalies
MONDO:0054791	leukodystrophy, hypomyelinating, 16
MONDO:0003267	myxopapillary ependymoma
MONDO:0003268	mixed glioma
MONDO:0030885	amyotrophic lateral sclerosis 26 with or without frontotemporal dementia
MONDO:0003269	subependymal giant cell astrocytoma
MONDO:0003263	childhood cerebellar neoplasm
MONDO:0003264	basosquamous carcinoma
MONDO:0003265	adjustment disorder
MONDO:0003266	ependymal tumor
MONDO:0003260	adult cerebellar neoplasm
MONDO:0003261	papillary meningioma of the cerebellum
MONDO:0003262	rhabdoid meningioma
MONDO:0015259	brachydactyly-mesomelia-intellectual disability-heart defects syndrome
MONDO:0015258	botulism
MONDO:0015257	sino-auricular heart block
MONDO:0015252	severe microbrachycephaly-intellectual disability-athetoid cerebral palsy syndrome
MONDO:0054860	deafness, autosomal recessive 110
MONDO:0030893	leukoencephalopathy, progressive, infantile-onset, with or without deafness
MONDO:0015251	balantidiasis
MONDO:0030895	nephrotic syndrome, type 22
MONDO:0015250	spinal atrophy-ophthalmoplegia-pyramidal syndrome
MONDO:0030894	AMED syndrome, digenic
MONDO:0015256	blepharoptosis-cleft palate-ectrodactyly-dental anomalies syndrome
MONDO:0015255	blepharophimosis-radioulnar synostosis syndrome
MONDO:0015254	schistosomiasis
MONDO:0054862	premature ovarian failure 15
MONDO:0015253	Diamond-Blackfan anemia
MONDO:0054861	intellectual disability, autosomal recessive 63
MONDO:0054846	epilepsy, familial adult myoclonic, 6
MONDO:0054845	developmental and epileptic encephalopathy, 66
MONDO:0054844	pontocerebellar hypoplasia, type 1D
MONDO:0054843	ciliary dyskinesia, primary, 38
MONDO:0003278	inner ear cancer
MONDO:0030897	Lessel-Kreienkamp syndrome
MONDO:0003279	testicular infarct
MONDO:0054849	inflammatory bowel disease 29
MONDO:0030896	chromosome 13q33-q34 deletion syndrome
MONDO:0030899	oculocutaneous albinism type 8
MONDO:0054847	epilepsy, familial adult myoclonic, 7
MONDO:0030898	immunodeficiency 76
MONDO:0003274	thoracic cancer
MONDO:0003275	middle ear cancer
MONDO:0003276	middle ear disease
MONDO:0003277	malignant ear neoplasm
MONDO:0003270	ganglioglioma
MONDO:0003271	iodine hypothyroidism
MONDO:0003272	mixed epithelial stromal tumor
MONDO:0003273	sternum cancer
MONDO:0015249	mitral atresia disorder
MONDO:0015248	ataxia-photosensitivity-short stature syndrome
MONDO:0015247	opsoclonus-myoclonus syndrome
MONDO:0015246	syndromic anorectal malformation
MONDO:0015241	arthrogryposis-like syndrome
MONDO:0015240	digitotalar dysmorphism
MONDO:0015245	rare intestinal disease
MONDO:0015244	autosomal recessive cerebellar ataxia
MONDO:0054852	peeling skin syndrome 6
MONDO:0015243	allergic bronchopulmonary aspergillosis
MONDO:0054850	ovarian dysgenesis 6
MONDO:0015242	aspergillosis
MONDO:0003249	pineal gland cancer
MONDO:0003245	aflatoxin-related hepatocellular carcinoma
MONDO:0003246	sclerosing hepatic carcinoma
MONDO:0003247	pineal parenchymal tumor of intermediate differentiation
MONDO:0003248	adult pineal parenchymal tumor
MONDO:0003241	central nervous system hemangioma
MONDO:0003242	fibrolamellar carcinoma
MONDO:0003243	hepatocellular clear cell carcinoma
MONDO:0003244	central nervous system mesenchymal non-meningothelial tumor
MONDO:0003240	thyroid gland disease
MONDO:0015238	arrhinia-choanal atresia-microphthalmia syndrome
MONDO:0015237	arrhinia
MONDO:0015236	aortic arch defects
MONDO:0015235	arachnodactyly-intellectual disability-dysmorphism syndrome
MONDO:0017897	autosomal recessive mendelian susceptibility to mycobacterial diseases due to a complete deficiency
MONDO:0017898	autosomal recessive mendelian susceptibility to mycobacterial diseases due to a partial deficiency
MONDO:0017899	autosomal dominant mendelian susceptibility to mycobacterial diseases due to a partial deficiency
MONDO:0015239	abnormal origin of the pulmonary artery
MONDO:0015230	anophthalmia-megalocornea-cardiopathy-skeletal anomalies syndrome
MONDO:0017893	inherited acute myeloid leukemia
MONDO:0017894	acute myeloid leukemia with CEBPA somatic mutations
MONDO:0017895	familial papillary or follicular thyroid carcinoma
MONDO:0017896	familial nonmedullary thyroid carcinoma
MONDO:0015234	arachnodactyly-abnormal ossification-intellectual disability syndrome
MONDO:0017890	tubulocystic renal cell carcinoma
MONDO:0015233	caudal appendage-deafness syndrome
MONDO:0017891	inherited renal cancer-predisposing syndrome
MONDO:0015232	radial deficiency-tibial hypoplasia syndrome
MONDO:0015231	Bartter syndrome
MONDO:0017892	autosomal recessive myogenic arthrogryposis multiplex congenita
MONDO:0054868	meconium ileus
MONDO:0054867	paraomphalocele
MONDO:0054866	sudden arrhythmia death syndrome
MONDO:0054865	encephalopathy due to mitochondrial and peroxisomal fission defect
MONDO:0003256	neurohypophysis granular cell tumor
MONDO:0003257	posterior pituitary gland neoplasm
MONDO:0003258	hobnail hemangioma
MONDO:0054869	nondystrophic myotonia
MONDO:0003259	melioidosis
MONDO:0003252	granular cell cancer
MONDO:0003253	vulvar granular cell tumor
MONDO:0003254	cardiac granular cell neoplasm
MONDO:0003255	mediastinal granular cell myoblastoma
MONDO:0003250	benign granular cell tumor
MONDO:0003251	esophageal granular cell tumor
MONDO:0015227	non-syndromic limb malformation
MONDO:0015226	syndrome with limb malformations as a major feature
MONDO:0015225	arthrogryposis syndrome
MONDO:0015224	rare intoxication
MONDO:0017886	MIT family translocation renal cell carcinoma
MONDO:0017887	renal cell carcinoma associated with neuroblastoma
MONDO:0015229	Bardet-Biedl syndrome
MONDO:0015228	pentasomy X
MONDO:0017889	mucinous tubular and spindle cell renal carcinoma
MONDO:0017882	Omsk hemorrhagic fever
MONDO:0017883	multilocular cystic clear cell renal cell neoplasm of low malignant potential
MONDO:0017884	papillary renal cell carcinoma
MONDO:0017885	chromophobe renal cell carcinoma
MONDO:0015223	rare anemia
MONDO:0015222	syndromic respiratory or mediastinal malformation
MONDO:0017880	Rift valley fever
MONDO:0015221	non-syndromic respiratory or mediastinal malformation
MONDO:0015220	syndrome with a central nervous system malformation as major feature
MONDO:0017881	Kyasanur forest disease
MONDO:0054813	Ehlers-Danlos syndrome, classic-like, 2
MONDO:0030846	spermatogenic failure 48
MONDO:0030847	arthrogryposis, distal, type 1C
MONDO:0054817	leukodystrophy, hypomyelinating, 17
MONDO:0015292	endotheliitis
MONDO:0015291	stromal keratitis
MONDO:0030841	mismatch repair cancer syndrome 3
MONDO:0015290	neurotrophic keratopathy
MONDO:0030844	spermatogenic failure 47
MONDO:0030843	mismatch repair cancer syndrome 4
MONDO:0030849	intellectual developmental disorder with speech delay and axonal peripheral neuropathy
MONDO:0015296	cardiac anomalies-heterotaxy syndrome
MONDO:0015295	intractable diarrhea-choanal atresia-eye anomalies syndrome
MONDO:0015294	nephrogenic systemic fibrosis
MONDO:0015293	segmental outgrowth-lipomatosis-arteriovenous malformation-epidermal nevus syndrome
MONDO:0015299	Asherman syndrome
MONDO:0015298	pellucid marginal degeneration
MONDO:0015297	microcephaly-digital anomalies-intellectual disability syndrome
MONDO:0054802	erythrocytosis, familial, 7
MONDO:0054801	erythrocytosis, familial, 6
MONDO:0030856	developmental and epileptic encephalopathy 89
MONDO:0030859	COACH syndrome 2
MONDO:0030858	immunodeficiency 75
MONDO:0015281	atrial standstill
MONDO:0054806	microcephaly 23, primary, autosomal recessive
MONDO:0015280	cardiofaciocutaneous syndrome
MONDO:0054805	microcephaly 22, primary, autosomal recessive
MONDO:0030852	neurodevelopmental disorder with dysmorphic facies, sleep disturbance, and brain abnormalities
MONDO:0054804	microcephaly 21, primary, autosomal recessive
MONDO:0030855	combined osteogenesis imperfecta and Ehlers-Danlos syndrome 2
MONDO:0030854	combined osteogenesis imperfecta and Ehlers-Danlos syndrome 1
MONDO:0015285	Carney complex
MONDO:0030860	neuronopathy, distal hereditary motor, type 5C
MONDO:0015284	heart-hand syndrome type 2
MONDO:0030862	COACH syndrome 3
MONDO:0015283	maternally-inherited cardiomyopathy and hearing loss
MONDO:0015282	cardiomyopathy-cataract-hip spine disease syndrome
MONDO:0030861	osteogenesis imperfecta, type 21
MONDO:0015289	infectious epithelial keratitis
MONDO:0015288	herpes simplex virus keratitis
MONDO:0015287	vulvar intraepithelial neoplasia
MONDO:0015286	congenital disorder of glycosylation
MONDO:0030868	spermatogenic failure 49
MONDO:0054835	parkinsonism-dystonia, infantile, 1
MONDO:0030867	thrombocytopenia 7
MONDO:0054833	charcot-marie-tooth disease, axonal, type 2DD
MONDO:0030869	spermatogenic failures 50
MONDO:0054832	corneal dystrophy, posterior polymorphous, 4
MONDO:0015270	butyrylcholinesterase deficiency
MONDO:0030864	Ritscher-Schinzel syndrome 3
MONDO:0003289	deep leiomyoma
MONDO:0054838	cardiomyopathy, familial hypertrophic 27
MONDO:0030866	neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities
MONDO:0054837	intellectual disability, autosomal dominant 57
MONDO:0054836	parkinsonism-dystonia, infantile, 2
MONDO:0003285	fallopian tube leiomyoma
MONDO:0003286	extrahepatic bile duct leiomyoma
MONDO:0003287	central nervous system leiomyoma
MONDO:0003288	bizarre leiomyoma
MONDO:0003281	ovarian cystic teratoma
MONDO:0003282	ovarian cyst
MONDO:0003283	epididymal neoplasm
MONDO:0003284	mediastinum leiomyoma
MONDO:0003280	swayback
MONDO:0015279	chronic mucocutaneous candidiasis
MONDO:0015274	chronic beryllium disease
MONDO:0030871	vertebral hypersegmentation and orofacial anomalies
MONDO:0015273	complete atrioventricular canal
MONDO:0030870	premature ovarian failure 17
MONDO:0015272	camptodactyly-taurinuria syndrome
MONDO:0030873	cardiofacioneurodevelopmental syndrome
MONDO:0015271	idiopathic camptocormia
MONDO:0030872	frontotemporal dementia and/or amyotrophic lateral sclerosis 8
MONDO:0015278	familial pancreatic carcinoma
MONDO:0054842	polycystic kidney disease 6 with or without polycystic liver disease
MONDO:0015277	medullary thyroid gland carcinoma
MONDO:0015276	prostate cancer
MONDO:0015275	partial atrioventricular canal
MONDO:0030878	Kaya-Barakat-Masson syndrome
MONDO:0030875	frontotemporal dementia and/or amyotrophic lateral sclerosis 5
MONDO:0030877	cardioacrofacial dysplasia 2
MONDO:0030876	cardioacrofacial dysplasia 1
MONDO:0003296	cellular leiomyoma
MONDO:0003297	gallbladder leiomyoma
MONDO:0003298	vulvar leiomyoma
MONDO:0003299	colorectal leiomyoma
MONDO:0003292	anus leiomyoma
MONDO:0003293	lung leiomyoma
MONDO:0003294	pericardium leiomyoma
MONDO:0003295	leiomyomatosis
MONDO:0003290	simple partial epilepsy
MONDO:0015269	symmetrical thalamic calcifications
MONDO:0003291	leiomyoma cutis
MONDO:0015268	medullary sponge kidney
MONDO:0015263	Brugada syndrome
MONDO:0015262	brachyolmia
MONDO:0015261	pseudopelade of Brocq
MONDO:0015260	diphyllobothriasis
MONDO:0030883	carpal tunnel syndrome 2
MONDO:0015267	Feingold syndrome
MONDO:0054831	Coffin-Siris syndrome 7
MONDO:0015266	brucellosis
MONDO:0015265	bronchiolitis obliterans with obstructive pulmonary disease
MONDO:0030880	mandibuloacral dysplasia progeroid syndrome
MONDO:0015264	cryptogenic organizing pneumonia
MONDO:0005846	microsporidiosis
MONDO:0005845	meningoencephalitis
MONDO:0030801	monosomy 7 myelodysplasia and leukemia syndrome 2
MONDO:0005848	miliary tuberculosis
MONDO:0005847	middle lobe syndrome
MONDO:0005842	maxillary sinusitis
MONDO:0005841	maxillary neoplasm
MONDO:0005844	chalazion
MONDO:0005843	mediastinal cancer
MONDO:0005840	mast-cell leukemia
MONDO:0017828	primary renal tubular acidosis
MONDO:0017829	autosomal dominant proximal renal tubular acidosis
MONDO:0017835	lymphocytic hypereosinophilic syndrome
MONDO:0017836	erythrokeratoderma en cocardes
MONDO:0017837	multiple sclerosis-ichthyosis-factor VIII deficiency syndrome
MONDO:0017838	sclerosteosis
MONDO:0017831	mild Canavan disease
MONDO:0017832	mycobacterium xenopi infection
MONDO:0017833	primary hypereosinophilic syndrome
MONDO:0017834	secondary hypereosinophilic syndrome
MONDO:0017830	severe Canavan disease
MONDO:0005839	Marburg hemorrhagic fever
MONDO:0005838	mansonelliasis
MONDO:0005857	morbillivirus infectious disease
MONDO:0005856	Mononegavirales infectious disease
MONDO:0005859	mucocutaneous leishmaniasis
MONDO:0005858	mucinous cystadenocarcinoma
MONDO:0005853	malignant mixed neoplasm
MONDO:0005852	mitral valve stenosis
MONDO:0005855	molluscum contagiosum
MONDO:0005854	mixed connective tissue disease
MONDO:0005851	Miller Fisher syndrome
MONDO:0005850	milker's nodule
MONDO:0017817	primary localized amyloidosis
MONDO:0017818	lethal arteriopathy syndrome due to fibulin-4 deficiency
MONDO:0017819	atypical dentin dysplasia due to SMOC2 deficiency
MONDO:0017824	familial isolated pituitary adenoma
MONDO:0017825	silent pituitary adenoma
MONDO:0017826	null pituitary adenoma
MONDO:0017827	malignant peripheral nerve sheath tumor
MONDO:0017820	obsolete disease with Cushing syndrome as a major feature
MONDO:0017821	functioning pituitary adenoma
MONDO:0017822	mixed functioning pituitary adenoma
MONDO:0017823	somatomammotropinoma
MONDO:0005849	milk allergic reaction
MONDO:0005824	Legionnaires' disease
MONDO:0005823	legionellosis
MONDO:0005826	lipid pneumonia
MONDO:0005825	leptospirosis
MONDO:0005820	Lassa fever
MONDO:0005822	latent syphilis
MONDO:0005821	late congenital syphilis
MONDO:0017806	15q overgrowth syndrome
MONDO:0017807	growing teratoma syndrome
MONDO:0017808	duplication of the pituitary gland
MONDO:0017809	parkinsonism due to ATP13A2 deficiency
MONDO:0017813	van Maldergem syndrome
MONDO:0017814	primary bone lymphoma
MONDO:0017815	acquired porencephaly
MONDO:0017816	primary systemic amyloidosis
MONDO:0017810	variant ABeta2M amyloidosis
MONDO:0017811	severe neonatal hypotonia-seizures-encephalopathy syndrome due to 5q31.3 microdeletion
MONDO:0017812	segmental progressive overgrowth syndrome with fibroadipose hyperplasia
MONDO:0005817	Kluver-Bucy syndrome
MONDO:0005816	Japanese encephalitis
MONDO:0005819	laryngeal tuberculosis
MONDO:0005818	Langerhans cell sarcoma
MONDO:0005835	Lynch syndrome
MONDO:0030835	developmental delay, impaired growth, dysmorphic facies, and axonal neuropathy
MONDO:0005834	lymphogranuloma venereum
MONDO:0005837	mandibular cancer
MONDO:0030837	neurodevelopmental disorder with microcephaly, impaired language, epilepsy, and gait abnormalities
MONDO:0005836	male reproductive organ cancer
MONDO:0005831	lymph node tuberculosis
MONDO:0005830	lumpy skin disease
MONDO:0005833	lymphatic system disease
MONDO:0005832	lymphangitis
MONDO:0017802	ovarian fibrothecoma
MONDO:0017803	primary progressive apraxia of speech
MONDO:0017804	autosomal recessive leukoencephalopathy-ischemic stroke-retinitis pigmentosa syndrome
MONDO:0017805	intellectual disability-hypotonia-brachycephaly-pyloric stenosis-cryptorchidism syndrome
MONDO:0017800	pseudo-Meigs syndrome
MONDO:0017801	atypical Meigs syndrome
MONDO:0030840	mismatch repair cancer syndrome 2
MONDO:0005828	listeriosis
MONDO:0005827	lipoatrophic diabetes
MONDO:0005829	louping ill
MONDO:0003227	prosopagnosia
MONDO:0005889	orthomyxoviridae infectious disease
MONDO:0003228	myelodysplastic/myeloproliferative neoplasm
MONDO:0003229	lymphedema
MONDO:0003223	meninges hemangiopericytoma
MONDO:0005886	oral candidiasis
MONDO:0003224	spindle cell hemangioma
MONDO:0005885	optic neuritis
MONDO:0003225	bone marrow disease
MONDO:0005888	ornithosis
MONDO:0005887	oral tuberculosis
MONDO:0003226	Nelson syndrome
MONDO:0005882	onchocerciasis
MONDO:0005881	oligohydramnios
MONDO:0003220	gallbladder carcinoma
MONDO:0005884	opisthorchiasis
MONDO:0003221	sclerosing hemangioma
MONDO:0003222	central nervous system melanocytic neoplasm
MONDO:0005883	ophthalmic herpes zoster
MONDO:0005880	oesophagostomiasis
MONDO:0017879	hantavirus pulmonary syndrome
MONDO:0015216	syndromic diaphragmatic or abdominal wall malformation
MONDO:0015215	non-syndromic diaphragmatic or abdominal wall malformation
MONDO:0015214	syndromic visceral malformation
MONDO:0015213	non-syndromic visceral malformation
MONDO:0017875	Bolivian hemorrhagic fever
MONDO:0015219	non-syndromic central nervous system malformation
MONDO:0017876	Venezuelan hemorrhagic fever
MONDO:0015218	syndromic developmental defect of the eye
MONDO:0017877	Brazilian hemorrhagic fever
MONDO:0017878	Chapare hemorrhagic fever
MONDO:0015217	non-syndromic developmental defect of the eye
MONDO:0017871	bilateral massive adrenal hemorrhage
MONDO:0017872	Lujo hemorrhagic fever
MONDO:0017873	Ebola hemorrhagic fever
MONDO:0017874	Argentine hemorrhagic fever
MONDO:0015212	syndromic intestinal malformation
MONDO:0015211	non-syndromic intestinal malformation
MONDO:0015210	syndromic gastroduodenal malformation
MONDO:0017870	supravalvular pulmonary stenosis
MONDO:0003238	cervical adenomyoma
MONDO:0003239	Camurati-Engelmann disease
MONDO:0003234	optic nerve astrocytoma
MONDO:0005897	paratyphoid fever
MONDO:0003235	optic nerve glioma
MONDO:0005896	Paramyxoviridae infectious disease
MONDO:0005899	parotid disease
MONDO:0003236	atypical polypoid adenomyoma
MONDO:0003237	adenomyoma of uterine corpus
MONDO:0005898	paronychia
MONDO:0005893	pancreatic endocrine carcinoma
MONDO:0003230	extraosseous Ewings sarcoma-primitive neuroepithelial tumor
MONDO:0003231	acute nonparalytic poliomyelitis
MONDO:0005892	otitis media with effusion
MONDO:0005895	paragonimiasis
MONDO:0003232	alcoholic pancreatitis
MONDO:0005894	paracoccidioidomycosis
MONDO:0003233	essential tremor
MONDO:0005891	ostertagiasis
MONDO:0005890	osteitis fibrosa
MONDO:0017868	diencephalic-mesencephalic junction dysplasia
MONDO:0015205	isolated lissencephaly type 1 without known genetic defects
MONDO:0015204	microlissencephaly
MONDO:0017869	chondroectodermal dysplasia with night blindness
MONDO:0015203	coronary artery congenital malformation
MONDO:0015202	babesiosis
MONDO:0015209	non-syndromic gastroduodenal malformation
MONDO:0017864	congenital pulmonary veins atresia or stenosis
MONDO:0015208	syndromic esophageal malformation
MONDO:0017865	congenital pulmonary valve stenosis
MONDO:0015207	non-syndromic esophageal malformation
MONDO:0017866	subpulmonary stenosis
MONDO:0017867	distal 17p13.1 microdeletion syndrome
MONDO:0015206	short stature-heart defect-craniofacial anomalies syndrome
MONDO:0017860	methanol poisoning
MONDO:0017861	ethylene glycol poisoning
MONDO:0017862	paraquat poisoning
MONDO:0017863	digitalis poisoning
MONDO:0015201	ankyloblepharon filiforme-imperforate anus syndrome
MONDO:0015200	anisakiasis
MONDO:0003205	renal pelvis adenocarcinoma
MONDO:0005868	myelophthisic anemia
MONDO:0005867	Mycoplasma pneumoniae pneumonia
MONDO:0003206	acquired hemangioma
MONDO:0003207	eccrine adenocarcinoma
MONDO:0003208	breast secretory carcinoma
MONDO:0005869	myiasis
MONDO:0005864	muscle cancer
MONDO:0003201	esophagus adenocarcinoma
MONDO:0003202	pituitary gland basophilic carcinoma
MONDO:0005866	mycobacterium avium complex disease
MONDO:0003203	pituitary carcinoma
MONDO:0005865	mushroom workers' lung
MONDO:0003204	villous adenocarcinoma
MONDO:0005862	multiple chemical sensitivity
MONDO:0005861	multidrug-resistant tuberculosis
MONDO:0003200	urethra adenocarcinoma
MONDO:0017857	spina bifida-hypospadias syndrome
MONDO:0017858	acute erythroid leukemia
MONDO:0017859	colchicine poisoning
MONDO:0017853	hypersensitivity pneumonitis
MONDO:0017854	T-b+ severe combined immunodeficiency
MONDO:0017855	T-B- severe combined immunodeficiency
MONDO:0017856	X-linked spasticity-intellectual disability-epilepsy syndrome
MONDO:0017850	sirenomelia
MONDO:0017851	erythrokeratodermia variabilis
MONDO:0017852	infantile spasms-broad thumbs syndrome
MONDO:0005879	ocular toxoplasmosis
MONDO:0003216	ureter adenocarcinoma
MONDO:0005878	ocular onchocerciasis
MONDO:0003217	ureter carcinoma
MONDO:0003218	adenocarcinoma in situ
MONDO:0003219	gastroesophageal junction adenocarcinoma
MONDO:0003212	nasal cavity carcinoma
MONDO:0005875	Newcastle disease
MONDO:0003213	ampulla of vater carcinoma
MONDO:0005874	neuroschistosomiasis
MONDO:0003214	apocrine adenocarcinoma
MONDO:0005877	nocardiosis
MONDO:0005876	Nidovirales infectious disease
MONDO:0003215	apocrine sweat gland cancer
MONDO:0005871	Nematoda infectious disease
MONDO:0005870	necatoriasis
MONDO:0003210	intrahepatic cholangiocarcinoma
MONDO:0005873	neuroaspergillosis
MONDO:0005872	nervous system cancer
MONDO:0003211	nasal cavity adenocarcinoma
MONDO:0017839	classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency, salt wasting form
MONDO:0017846	autosomal dominant spastic ataxia
MONDO:0017847	autosomal recessive spastic ataxia
MONDO:0017848	partial deletion of the short arm of chromosome 12
MONDO:0017849	Siegler-Brewer-Carey syndrome
MONDO:0017842	Senior-Loken syndrome
MONDO:0017843	congenital pulmonary sequestration
MONDO:0017844	Sezary syndrome
MONDO:0017845	spastic ataxia
MONDO:0017840	classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency, simple virilizing form
MONDO:0017841	autoimmune disease with skin involvement
MONDO:0003209	thymus gland adenocarcinoma
MONDO:0015090	autosomal recessive pure spastic paraplegia
MONDO:0015094	subependymal nodular heterotopia
MONDO:0015093	sub-cortical nodular heterotopia
MONDO:0015092	cleft hard palate
MONDO:0015091	autosomal dominant spastic paraplegia type 9
MONDO:0015098	situs inversus totalis
MONDO:0015097	aortic valve dysplasia
MONDO:0015096	familial hypofibrinogenemia
MONDO:0015095	Peters anomaly-cataract syndrome
MONDO:0015099	unilateral hemispheric polymicrogyria
MONDO:0015083	nuclear oculomotor paralysis
MONDO:0015082	alopecia antibody deficiency
MONDO:0015081	neuroendocrine tumor with other location
MONDO:0015080	thymic tumor
MONDO:0027069	mitochondrial complex 5 (ATP synthase) deficiency, mitochondrial type 1
MONDO:0027068	mitochondrial complex 1 deficiency, mitochondrial type 1
MONDO:0054691	immunodeficiency, common variable, 14
MONDO:0015087	autosomal dominant complex spastic paraplegia
MONDO:0054695	myopathy, centronuclear, 6, with fiber-type disproportion
MONDO:0015086	cloverleaf skull-asphyxiating thoracic dysplasia syndrome
MONDO:0015085	bathing suit ichthyosis
MONDO:0015084	FRAXF syndrome
MONDO:0054699	proteasome-associated autoinflammatory syndrome 3
MONDO:0054698	proteasome-associated autoinflammatory syndrome 1
MONDO:0054697	immunodeficiency 11b with atopic dermatitis
MONDO:0015089	autosomal recessive complex spastic paraplegia
MONDO:0015088	autosomal dominant pure spastic paraplegia
MONDO:0054696	immunodeficiency 53
MONDO:0015072	liver neuroendocrine carcinoma
MONDO:0015071	middle ear neuroendocrine tumor
MONDO:0015070	laryngeal neuroendocrine neoplasm
MONDO:0003087	mucoepidermoid breast carcinoma
MONDO:0003088	intramuscular hemangioma
MONDO:0003089	extrahepatic bile duct mucoepidermoid carcinoma
MONDO:0003083	venous hemangioma
MONDO:0003084	uremic neuropathy
MONDO:0003085	keratitis
MONDO:0003086	thymic mucoepidermoid carcinoma
MONDO:0003080	indolent systemic mastocytosis
MONDO:0003081	thalamic disease
MONDO:0003082	filamentary keratitis
MONDO:0015076	rare parathyroid tumor
MONDO:0015075	thyroid gland carcinoma
MONDO:0015074	thyroid tumor
MONDO:0015073	gallbladder neuroendocrine tumor, grade 1/2
MONDO:0015079	multiple polyglandular tumor
MONDO:0015078	gastroenteropancreatic neuroendocrine neoplasm
MONDO:0015077	adrenal/paraganglial tumor
MONDO:0015061	neurogenic thoracic outlet syndrome
MONDO:0015060	mosaic trisomy 3
MONDO:0003098	mediastinal neural neoplasm
MONDO:0003099	endophthalmitis
MONDO:0003094	mucoepidermoid thyroid carcinoma
MONDO:0027048	deafness, Y-linked 2
MONDO:0003095	laryngeal mucoepidermoid carcinoma
MONDO:0003096	deep hemangioma
MONDO:0003097	childhood mediastinal neurogenic neoplasm
MONDO:0003090	extrahepatic bile duct carcinoma
MONDO:0003091	cutaneous mucoepidermoid carcinoma
MONDO:0003092	lacrimal gland mucoepidermoid carcinoma
MONDO:0003093	mucoepidermoid esophageal carcinoma
MONDO:0015065	ileal neuroendocrine tumor, well differentiated, low or intermediate grade
MONDO:0015064	jejunal neuroendocrine tumor, well differentiated, low or intermediate grade
MONDO:0015063	duodenal neuroendocrine tumor, well differentiated, low or intermediate grade
MONDO:0015062	gastric neuroendocrine tumor, well differentiated, low or intermediate grade
MONDO:0015069	neuroendocrine tumor of the anal canal
MONDO:0015068	neuroendocrine tumor of rectum, well differentiated, low or intermediate grade
MONDO:0015067	neuroendocrine tumor of the colon, well differentiated, low or intermediate grade tumor
MONDO:0015066	neuroendocrine tumor of the appendix, well differentiated, low or intermediate grade
MONDO:0054666	ovarian dysgenesis 5
MONDO:0054665	pituitary adenoma 3, multiple types
MONDO:0054654	combined oxidative phosphorylation deficiency 32
MONDO:0027091	xanthogranulomatous sialadenitis
MONDO:0054680	epiphyseal dysplasia, multiple, 7
MONDO:0054669	pontocerebellar hypoplasia, type 11
MONDO:0054677	combined oxidative phosphorylation deficiency 33
MONDO:0054736	mosaic variegated aneuploidy syndrome 3
MONDO:0054733	spermatogenic failure 29
MONDO:0003146	ependymoblastoma
MONDO:0054739	Fraser syndrome 3
MONDO:0003147	space motion sickness
MONDO:0003148	SM-AHNMD
MONDO:0054738	Fraser syndrome 2
MONDO:0003149	aggressive systemic mastocytosis
MONDO:0054737	Fraser syndrome 1
MONDO:0003142	intracranial primitive neuroectodermal tumor
MONDO:0003143	angiokeratoma
MONDO:0003144	medulloepithelioma
MONDO:0003145	supratentorial primitive neuroectodermal tumor
MONDO:0003140	immune-complex glomerulonephritis
MONDO:0003141	cerebellopontine angle embryonal tumor
MONDO:0015139	rare epilepsy
MONDO:0015138	rare genetic primary immunodeficiency
MONDO:0015137	periodic fever syndrome
MONDO:0015136	immunodeficiency due to a genetic complement cascade protein anomaly
MONDO:0017798	Spigelian hernia-cryptorchidism syndrome
MONDO:0017799	Meigs syndrome
MONDO:0017794	Xq12-q13.3 duplication syndrome
MONDO:0015131	congenital combined immunodeficiency
MONDO:0017795	ameloblastoma
MONDO:0015130	acquired chronic primary adrenal insufficiency
MONDO:0017796	ameloblastic carcinoma
MONDO:0017797	rare odontologic tumor
MONDO:0017790	gastric adenocarcinoma and proximal polyposis of the stomach
MONDO:0054743	polycystic liver disease 3 with or without kidney cysts
MONDO:0015135	primary immunodeficiency due to a genetic defect in innate immunity
MONDO:0054742	combined oxidative phosphorylation deficiency 35
MONDO:0015134	constitutional neutropenia
MONDO:0017791	high bone mass osteogenesis imperfecta
MONDO:0015133	quantitative and/or qualitative congenital phagocyte defect
MONDO:0054741	combined oxidative phosphorylation deficiency 34
MONDO:0017792	7p22.1 microduplication syndrome
MONDO:0054740	blepharocheilodontic syndrome 1
MONDO:0015132	immunodeficiency predominantly affecting antibody production
MONDO:0017793	marfanoid habitus-inguinal hernia-advanced bone age syndrome
MONDO:0054725	spermatogenic failure 21
MONDO:0054724	spermatogenic failure 20
MONDO:0054723	spermatogenic failure 19
MONDO:0054722	geleophysic dysplasia 3
MONDO:0003157	disappearing bone disease
MONDO:0054729	spermatogenic failure 25
MONDO:0003158	malignant myoepithelioma
MONDO:0054728	spermatogenic failure 24
MONDO:0003159	vascular hemostatic disease
MONDO:0054727	spermatogenic failure 23
MONDO:0054726	spermatogenic failure 22
MONDO:0003153	adult brainstem glioma
MONDO:0003154	hemangioma of peripheral nerve
MONDO:0003155	cavernous hemangioma
MONDO:0003156	adenosquamous carcinoma
MONDO:0003150	male reproductive system disease
MONDO:0003151	movement disease
MONDO:0003152	adult brainstem gliosarcoma
MONDO:0015128	primary adrenal insufficiency
MONDO:0015127	pituitary deficiency
MONDO:0015126	polyendocrinopathy
MONDO:0015125	rare thyroid disease
MONDO:0017787	erythroderma desquamativum
MONDO:0017788	contractures - webbed neck - micrognathia - hypoplastic nipples syndrome
MONDO:0017789	idiopathic linear interstitial keratitis
MONDO:0015129	chronic primary adrenal insufficiency
MONDO:0017783	congenital pancreatic cyst
MONDO:0015120	rare acquired eye disease
MONDO:0017784	Epstein-Barr virus-associated gastric carcinoma
MONDO:0017785	PENS syndrome
MONDO:0017786	2q23.1 microduplication syndrome
MONDO:0054732	spermatogenic failure 28
MONDO:0015124	rare adrenal disease
MONDO:0017780	20p13 microdeletion syndrome
MONDO:0015123	rare inherited dyslipidemia
MONDO:0054731	spermatogenic failure 27
MONDO:0017781	12p12.1 microdeletion syndrome
MONDO:0015122	rare diabetes mellitus
MONDO:0054730	spermatogenic failure 26
MONDO:0017782	developmental and speech delay due to SOX5 deficiency
MONDO:0015121	rare eye tumor
MONDO:0003128	classic pulmonary blastoma
MONDO:0003129	epithelial predominant pulmonary blastoma
MONDO:0003124	testicular Leydig cell tumor
MONDO:0005787	hepatic tuberculosis
MONDO:0003125	testicular sex cord-stromal neoplasm
MONDO:0005786	Hepadnaviridae infectious disease
MONDO:0005789	hepatitis D virus infection
MONDO:0003126	breast hemangioma
MONDO:0005788	hepatitis E virus infection
MONDO:0003127	embryoma
MONDO:0003120	mixed testicular germ cell cancer
MONDO:0005783	hemopericardium
MONDO:0003121	middle cranial fossa meningioma
MONDO:0005782	HELLP syndrome
MONDO:0003122	striatonigral degeneration
MONDO:0005785	henipavirus infectious disease
MONDO:0005784	hantavirus hemorrhagic fever with renal syndrome
MONDO:0003123	multiple system atrophy
MONDO:0005781	hantavirus pulmonary syndrome
MONDO:0005780	hantavirus infectious disease
MONDO:0015117	rare hepatic and biliary tract tumor
MONDO:0015116	rare biliary tract disease
MONDO:0015115	rare genetic metabolic liver disease
MONDO:0015114	rare parenchymal liver disease
MONDO:0017776	nocardiosis
MONDO:0017777	rat-bite fever
MONDO:0017778	lamellar ichthyosis
MONDO:0015119	bronchopulmonary tumor
MONDO:0017779	alpha-N-acetylgalactosaminidase deficiency
MONDO:0015118	rare pulmonary disease
MONDO:0017772	oral erosive lichen
MONDO:0054761	microcephaly 20, primary, autosomal recessive
MONDO:0017773	hypoalphalipoproteinemia
MONDO:0017774	hypobetalipoproteinemia
MONDO:0017775	melioidosis
MONDO:0054765	amyloidosis, primary localized cutaneous, 3
MONDO:0015113	rare vascular liver disease
MONDO:0015112	rare pancreatic disease
MONDO:0054764	neurodegeneration with brain iron accumulation 8
MONDO:0015111	gastroesophageal disease
MONDO:0017770	Robinow-like syndrome
MONDO:0054763	neurodegeneration with brain iron accumulation 7
MONDO:0015110	genetic cardiac rhythm disease
MONDO:0017771	Mayer-Rokitansky-Kuster-Hauser syndrome
MONDO:0003139	mesangial proliferative glomerulonephritis
MONDO:0003135	focal embolic glomerulonephritis
MONDO:0005798	HIV-associated nephropathy
MONDO:0005797	HIV wasting syndrome
MONDO:0003136	anti-basement membrane glomerulonephritis
MONDO:0003137	diffuse glomerulonephritis
MONDO:0054749	body mass index quantitative trait locus 19
MONDO:0003138	subacute glomerulonephritis
MONDO:0005799	hookworm infectious disease
MONDO:0054748	Fanconi anemia, complementation group S
MONDO:0005794	Herpesviridae infectious disease
MONDO:0003131	congenital mesoblastic nephroma
MONDO:0005793	herpes simplex virus keratitis
MONDO:0003132	rapidly progressive glomerulonephritis
MONDO:0005796	HIV enteropathy
MONDO:0003133	exudative glomerulonephritis
MONDO:0003134	proliferative glomerulonephritis
MONDO:0005795	histoplasmosis
MONDO:0005790	hepatitis A virus infection
MONDO:0005792	herpes simplex virus gingivostomatitis
MONDO:0003130	mesoblastic nephroma
MONDO:0005791	herpangina
MONDO:0017769	acquired immunodeficiency
MONDO:0015106	rare urogenital disease
MONDO:0015105	African tick typhus
MONDO:0015104	porphyria cutanea tarda
MONDO:0015103	pulmonary valve agenesis-tetralogy of fallot-absence of ductus arteriosus syndrome
MONDO:0017765	disorder of magnesium transport
MONDO:0017766	disorder of manganese transport
MONDO:0015109	congenital anomaly of the mitral subvalvular apparatus
MONDO:0017767	rheumatic fever
MONDO:0015108	rare non-syndromic intellectual disability
MONDO:0017768	reflex epilepsy
MONDO:0015107	rare genetic eye disease
MONDO:0017761	disorder of mineral absorption and transport
MONDO:0054750	amyotrophic lateral sclerosis, susceptibility to, 24
MONDO:0017762	disorder of copper metabolism
MONDO:0017763	disorder of iron metabolism and transport
MONDO:0017764	disorder of zinc metabolism
MONDO:0054754	encephalopathy, acute, infection-induced (herpes-specific), susceptibility to, 8
MONDO:0015102	non-secreting chemodectoma
MONDO:0015101	Marin-Amat syndrome
MONDO:0015100	aregenerative anemia
MONDO:0054752	multiple synostoses syndrome 4
MONDO:0017760	disorder of other vitamins and cofactors metabolism and transport
MONDO:0015171	congenital enterocyte heparan sulfate deficiency
MONDO:0030720	trichomonal vulvovaginitis
MONDO:0015170	congenital sodium diarrhea
MONDO:0003186	esophageal adenoid cystic carcinoma
MONDO:0003187	Bartholin gland adenoid cystic carcinoma
MONDO:0003188	juvenile myoclonic epilepsy
MONDO:0003189	middle ear adenocarcinoma
MONDO:0003182	anterior horn disease
MONDO:0003183	trachea adenoid cystic carcinoma
MONDO:0003184	trachea carcinoma
MONDO:0003185	adenoid cystic breast carcinoma
MONDO:0042705	prostatic malacoplakia associated with prostatic abscess
MONDO:0003180	cutaneous adenocystic carcinoma
MONDO:0003181	lung adenoid cystic carcinoma
MONDO:0015175	autoimmune pancreatitis
MONDO:0015174	autoimmune enteropathy type 3
MONDO:0015173	autoimmune enteropathy type 2
MONDO:0015172	epithelio-exfoliative colitis-deafness syndrome
MONDO:0015179	intestinal disease due to vitamin absorption anomaly
MONDO:0015178	congenital intestinal transport defect
MONDO:0015177	metaphyseal anadysplasia
MONDO:0015176	undetermined colitis
MONDO:0015160	multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome
MONDO:0003197	granular cell carcinoma
MONDO:0003198	small intestine adenocarcinoma
MONDO:0003199	anal carcinoma
MONDO:0003193	bile duct adenocarcinoma
MONDO:0003194	hemangioma of lung
MONDO:0003195	peritoneal serous adenocarcinoma
MONDO:0003196	appendix carcinoma
MONDO:0003190	middle ear carcinoma
MONDO:0003191	rete ovarii adenocarcinoma
MONDO:0015169	chronic diarrhea due to glucoamylase deficiency
MONDO:0042717	Saul-Wilkes-Stevenson syndrome
MONDO:0003192	rete ovarii neoplasm
MONDO:0015164	acute myeloid leukemia and myelodysplastic syndromes related to alkylating agent
MONDO:0015163	primary glomerular disease
MONDO:0015162	rare syndromic intellectual disability
MONDO:0015161	multiple congenital anomalies/dysmorphic syndrome without intellectual disability
MONDO:0015168	arthrogryposis multiplex congenita
MONDO:0015167	amniotic band syndrome
MONDO:0015166	acute myeloid leukemia with t(8;21)(q22;q22) translocation
MONDO:0015165	acute myeloid leukemia and myelodysplastic syndromes related to topoisomerase type 2 inhibitor
MONDO:0003168	cerebellar pilocytic astrocytoma
MONDO:0003169	diencephalic astrocytomas
MONDO:0054716	microcephaly 19, primary, autosomal recessive
MONDO:0003164	cauda equina neoplasm
MONDO:0003165	cerebellar astrocytoma
MONDO:0003166	pilocytic astrocytoma
MONDO:0003167	pleomorphic xanthoastrocytoma
MONDO:0003160	sebaceous carcinoma
MONDO:0003161	benign ependymoma
MONDO:0003162	pilomyxoid astrocytoma
MONDO:0003163	cauda equina intradural extramedullary astrocytoma
MONDO:0042726	macrogyria, pseudobulbar palsy and intellectual disability
MONDO:0042727	sacrococcygeal teratoma
MONDO:0015159	multiple congenital anomalies/dysmorphic syndrome-intellectual disability
MONDO:0015158	unexplained periodic fever syndrome
MONDO:0042724	macrocephaly, intellectual disability, short stature, spastic paraplegia and cns malformations
MONDO:0015153	autosomal monosomy
MONDO:0015152	autosomal recessive limb-girdle muscular dystrophy
MONDO:0015151	muscular dystrophy, limb-girdle, autosomal dominant
MONDO:0015150	complex hereditary spastic paraplegia
MONDO:0015157	human herpesvirus 8-related tumor
MONDO:0015156	typhus-group rickettsiosis
MONDO:0015155	spotted fever rickettsiosis
MONDO:0015154	rickettsial disease
MONDO:0054701	Kleefstra syndrome 2
MONDO:0054700	proteasome-associated autoinflammatory syndrome 2
MONDO:0003179	lacrimal gland adenoid cystic carcinoma
MONDO:0003175	salivary gland adenoid cystic carcinoma
MONDO:0003176	cervical adenoid cystic carcinoma
MONDO:0003177	prostate adenoid cystic carcinoma
MONDO:0054708	retinitis pigmentosa 80
MONDO:0003178	laryngeal adenoid cystic carcinoma
MONDO:0003171	pineal gland astrocytoma
MONDO:0003172	glomeruloid hemangioma
MONDO:0003173	brain stem astrocytic neoplasm
MONDO:0003174	spinal cord astrocytoma
MONDO:0015149	pure hereditary spastic paraplegia
MONDO:0015148	lissencephaly type 3
MONDO:0003170	gliofibroma
MONDO:0015147	other syndrome with lissencephaly as a major feature
MONDO:0015142	ataxia syndrome
MONDO:0015141	disorder of medulla oblongata
MONDO:0015140	early-onset autosomal dominant Alzheimer disease
MONDO:0015146	classic lissencephaly
MONDO:0015145	neurovascular malformation
MONDO:0015144	brain inflammatory disease
MONDO:0015143	rare movement disorder
MONDO:0005725	cyclosporiasis
MONDO:0005724	cryptococcosis
MONDO:0005727	cystoisosporiasis
MONDO:0005726	cysticercosis
MONDO:0005721	coxsackievirus infectious disease
MONDO:0005720	cowpox
MONDO:0005723	Cryptococcal meningitis
MONDO:0005722	croup
MONDO:0017707	disorder of lipid metabolism
MONDO:0017708	mevalonate kinase deficiency
MONDO:0017709	disorder of lipid absorption and transport
MONDO:0017714	acyl-CoA dehydrogenase deficiency
MONDO:0017715	3-hydroxyacyl-CoA dehydrogenase deficiency
MONDO:0017716	disorder of carnitine cycle and carnitine transport
MONDO:0017717	metabolic disease due to other fatty acid oxidation disorder
MONDO:0017710	congenital systemic veins anomaly
MONDO:0017711	pancreatic colipase deficiency
MONDO:0017712	combined pancreatic lipase-colipase deficiency
MONDO:0017713	disorder of fatty acid oxidation and ketogenesis
MONDO:0005718	Coronaviridae infectious disease
MONDO:0005717	contagious pustular dermatitis
MONDO:0005719	Coronavinae infectious disease
MONDO:0005736	eastern equine encephalitis
MONDO:0005735	dracunculiasis
MONDO:0005738	echinococcosis
MONDO:0005737	Ebola hemorrhagic fever
MONDO:0005732	diphyllobothriasis
MONDO:0005731	dipetalonemiasis
MONDO:0005734	dourine
MONDO:0005733	dirofilariasis
MONDO:0005730	Dictyocaulus infectious disease
MONDO:0017703	disorder of glyoxylate metabolism
MONDO:0017704	familial partial epilepsy
MONDO:0017705	congenital pulmonary venous return anomaly
MONDO:0017706	disorder of carbohydrate absorption and transport
MONDO:0017700	glycogen storage disease due to glycogen branching enzyme deficiency, childhood neuromuscular form
MONDO:0017701	glycogen storage disease due to glycogen branching enzyme deficiency, adult neuromuscular form
MONDO:0017702	glycerol kinase deficiency
MONDO:0005729	dicrocoeliasis
MONDO:0005728	diaphragm disease
MONDO:0005703	Churg-Strauss syndrome
MONDO:0030703	autoimmune vasculitis
MONDO:0030702	autoimmune atherosclerosis
MONDO:0005702	chromoblastomycosis
MONDO:0005705	clonorchiasis
MONDO:0030705	Trichomonas prostatitis
MONDO:0005704	Ciliophora infectious disease
MONDO:0005701	chlamydia trachomatis infectious disease
MONDO:0030701	autoimmune cardiomyopathy
MONDO:0005700	chickenpox
MONDO:0030700	autoimmune glomerulonephritis
MONDO:0030707	Trichomonas balanoposthitis
MONDO:0030706	Trichomonas cystitis
MONDO:0030708	Trichomonas cervicitis
MONDO:0005714	congenital syphilis
MONDO:0005716	contagious pleuropneumonia
MONDO:0005715	congenital toxoplasmosis
MONDO:0005710	composite lymphoma
MONDO:0005712	congenital nystagmus
MONDO:0005711	congenital diaphragmatic hernia
MONDO:0005707	coccidiosis
MONDO:0005706	coccidioidomycosis
MONDO:0005709	common cold
MONDO:0005708	Colorado tick fever
MONDO:0005769	geniculate herpes zoster
MONDO:0003106	verrucous keratotic hemangioma
MONDO:0005768	gastrointestinal tuberculosis
MONDO:0003107	infratentorial cancer
MONDO:0003108	cervicomedullary junction neoplasm
MONDO:0003109	foramen magnum meningioma
MONDO:0005765	foot and mouth disease
MONDO:0003102	perineurioma
MONDO:0003103	nerve root neoplasm
MONDO:0005764	follicular dendritic cell sarcoma
MONDO:0005767	gas gangrene
MONDO:0003104	epicardium cancer
MONDO:0005766	fungal lung infectious disease
MONDO:0003105	prostate disease
MONDO:0005761	filarial elephantiasis
MONDO:0005760	fibroepithelial neoplasm
MONDO:0005763	Flaviviridae infectious disease
MONDO:0003100	nerve plexus neoplasm
MONDO:0003101	intraneural perineurioma
MONDO:0005762	Filoviridae infectious disease
MONDO:0017758	disorder of vitamin and non-protein cofactor absorption and transport
MONDO:0017759	disorder of catecholamine synthesis
MONDO:0017754	inborn disorder of porphyrin metabolism
MONDO:0017755	inborn disorder of bilirubin metabolism
MONDO:0017756	disorder of pterin metabolism
MONDO:0017757	disorder of metabolite absorption and transport
MONDO:0017750	defect in conserved oligomeric Golgi complex
MONDO:0017751	Reye syndrome
MONDO:0017752	defect in V-ATPase
MONDO:0017753	disorder of peroxisomal alpha-, beta- and omega-oxidation
MONDO:0003117	somatoform disorder
MONDO:0005779	hand, foot and mouth disease
MONDO:0003118	testicular Brenner tumor
MONDO:0003119	histiocytoid hemangioma
MONDO:0003113	extragonadal germ cell cancer
MONDO:0005776	gnathomiasis
MONDO:0003114	bone giant cell sarcoma
MONDO:0005775	G6PD deficiency
MONDO:0003115	subglottic hemangioma
MONDO:0005778	haemonchiasis
MONDO:0005777	granuloma inguinale
MONDO:0003116	calciphylaxis
MONDO:0005772	geotrichosis
MONDO:0005771	geographic tongue
MONDO:0003110	skin hemangioma
MONDO:0005774	glanders
MONDO:0003111	gastric neuroendocrine neoplasm
MONDO:0005773	Gerstmann syndrome
MONDO:0003112	malignant gastric germ cell tumor
MONDO:0005770	genital herpes
MONDO:0017747	disorder of fucoglycosan synthesis
MONDO:0017748	inborn disorder of glycosphingolipid and glycosylphosphatidylinositol anchor glycosylation
MONDO:0017749	disorder of multiple glycosylation
MONDO:0017743	disorder of O-N-acetylgalactosaminylglycan synthesis
MONDO:0017744	disorder of O-xylosyl/N-acetylgalactosaminylglycan synthesis
MONDO:0017745	disorder of O-mannosylglycan synthesis
MONDO:0017746	atypical Rett syndrome
MONDO:0017740	disorder of protein N-glycosylation
MONDO:0017741	disorder of protein O-glycosylation
MONDO:0017742	disorder of O-xylosylglycan synthesis
MONDO:0005747	enterovirus infectious disease
MONDO:0005746	enterobiasis
MONDO:0005749	eosinophilic pneumonia
MONDO:0005748	enzootic pneumonia of calves
MONDO:0005743	encephalitozoonosis
MONDO:0005742	emphysematous cholecystitis
MONDO:0005745	Enoplea infectious disease
MONDO:0005744	yolk sac tumor
MONDO:0005741	egg allergy
MONDO:0005740	Echovirus infectious disease
MONDO:0017729	metachromatic leukodystrophy, late infantile form
MONDO:0017736	disorder of sialic acid metabolism
MONDO:0017737	intermediate severe Salla disease
MONDO:0017738	lysosomal glycogen storage disease
MONDO:0017739	disorder of lysosomal-related organelles
MONDO:0017732	alpha-mannosidosis, infantile form
MONDO:0017733	alpha-mannosidosis, adult form
MONDO:0017734	sialidosis
MONDO:0017735	congenital aortic valve stenosis
MONDO:0017730	metachromatic leukodystrophy, adult form
MONDO:0017731	glycoproteinosis
MONDO:0005739	echinostomiasis
MONDO:0005758	eunuchism
MONDO:0005757	eumycotic mycetoma
MONDO:0005759	fascioloidiasis
MONDO:0005754	epilepsy with generalized tonic-clonic seizures
MONDO:0005753	epiglottitis
MONDO:0005756	ethmoid sinusitis
MONDO:0005755	equine infectious anemia
MONDO:0005750	ephemeral fever
MONDO:0005752	epidural abscess
MONDO:0005751	epidemic pleurodynia
MONDO:0017718	mitochondrial disorder due to a defect in assembly or maturation of the respiratory chain complexes
MONDO:0017719	gangliosidosis
MONDO:0017725	Tay-Sachs disease, b variant, juvenile form
MONDO:0017726	Tay-Sachs disease, b variant, adult form
MONDO:0017727	fixed subaortic stenosis
MONDO:0017728	Tay-Sachs disease, B1 variant
MONDO:0017721	Sandhoff disease, infantile form
MONDO:0017722	Sandhoff disease, juvenile form
MONDO:0017723	Sandhoff disease, adult form
MONDO:0017724	Tay-Sachs disease, b variant, infantile form
MONDO:0017720	GM2 gangliosidosis
MONDO:0054581	Townes-Brocks syndrome 1
MONDO:0054582	Townes-Brocks syndrome 2
MONDO:0054588	Noonan syndrome-like disorder with loose anagen hair 2
MONDO:0054573	Lopes-Maciel-Rodan syndrome
MONDO:0054577	bleeding disorder, platelet-type, 21
MONDO:0054591	Stankiewicz-Isidor syndrome
MONDO:0054593	microcephaly 18, primary, autosomal dominant
MONDO:0054559	congenital disorder of glycosylation, type IIq
MONDO:0054561	anauxetic dysplasia 2
MONDO:0054560	anauxetic dysplasia 1
MONDO:0054565	short-rib thoracic dysplasia 17 with or without polydactyly
MONDO:0054549	peroxisome biogenesis disorder 10B
MONDO:0054551	avascular necrosis of femoral head, primary, 2
MONDO:0054550	avascular necrosis of femoral head, primary, 1
MONDO:0003029	skin angiosarcoma
MONDO:0054615	spermatogenic failure 18
MONDO:0003025	conventional angiosarcoma
MONDO:0005688	campylobacteriosis
MONDO:0005687	Caliciviridae infectious disease
MONDO:0003026	gallbladder angiosarcoma
MONDO:0003027	thyroid gland angiosarcoma
MONDO:0003028	thyroid sarcoma
MONDO:0005689	cannabis dependence
MONDO:0003021	central nervous system angiosarcoma
MONDO:0005684	bulbar polio
MONDO:0003022	pediatric angiosarcoma
MONDO:0005683	brucellosis
MONDO:0003023	aorta angiosarcoma
MONDO:0005686	Bunyaviridae infectious disease
MONDO:0005685	bullous pemphigoid
MONDO:0003024	breast angiosarcoma
MONDO:0005680	Brill-Zinsser disease
MONDO:0005682	bronchopneumonia
MONDO:0003020	orofaciodigital syndrome
MONDO:0015018	ichthyosis, congenital, autosomal recessive 12
MONDO:0015017	anterior segment dysgenesis 8
MONDO:0015016	anterior segment dysgenesis 6
MONDO:0015015	congenital bile acid synthesis defect 6
MONDO:0017677	focal acral hyperkeratosis
MONDO:0017678	obsolete disease with punctate palmoplantar keratoderma as a major feature
MONDO:0017679	obsolete autosomal dominant disease associated with punctate palmoplantar keratoderma as a major feature
MONDO:0015019	susceptibility to Yao syndrome
MONDO:0017673	isolated focal palmoplantar keratoderma
MONDO:0015010	atypical glycine encephalopathy
MONDO:0017674	disease with focal palmoplantar keratoderma as a major feature
MONDO:0017675	punctate palmoplantar keratoderma
MONDO:0017676	marginal papular palmoplantar keratoderma
MONDO:0015014	coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, and deafness
MONDO:0015013	retinitis pigmentosa 77
MONDO:0017670	autosomal dominant diffuse mutilating palmoplantar keratoderma
MONDO:0017671	autosomal recessive disease with diffuse palmoplantar keratoderma as a major feature
MONDO:0015012	mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders
MONDO:0017672	focal palmoplantar keratoderma
MONDO:0015011	optic atrophy 11
MONDO:0054602	gaze palsy, familial horizontal, with progressive scoliosis, 2
MONDO:0054601	pituitary adenoma 5, multiple types
MONDO:0003036	mucoepidermoid carcinoma
MONDO:0005699	cervicofacial actinomycosis
MONDO:0005698	cervical incompetence
MONDO:0003037	hypotrichosis
MONDO:0003038	dysgraphia
MONDO:0003039	nominal aphasia
MONDO:0005695	central nervous system AIDS arteritis
MONDO:0003032	superior vena cava angiosarcoma
MONDO:0003033	prostate angiosarcoma
MONDO:0005694	cecal neoplasm
MONDO:0003034	mediastinum angiosarcoma
MONDO:0005697	cerebral toxoplasmosis
MONDO:0005696	central nervous system tuberculosis
MONDO:0003035	ovarian angiosarcoma
MONDO:0005691	cardiovirus infectious disease
MONDO:0005690	Caplan syndrome
MONDO:0005693	cauda equina syndrome
MONDO:0003030	endometrioid stromal sarcoma of the cervix
MONDO:0003031	endometrioid stromal and related neoplasms of the cervix
MONDO:0005692	cat-scratch disease
MONDO:0015007	spastic paraplegia, intellectual disability, nystagmus, and obesity;
MONDO:0015006	generalized basal epidermolysis bullosa simplex with skin atrophy, scarring and hair loss
MONDO:0015005	epilepsy, early-onset, vitamin B6-dependent
MONDO:0015004	dystonia 28, childhood-onset
MONDO:0017666	diffuse palmoplantar keratoderma
MONDO:0017667	isolated diffuse palmoplantar keratoderma
MONDO:0015009	lymphatic malformation 7
MONDO:0017668	intellectual disability-short stature-hypertelorism syndrome
MONDO:0017669	disease with diffuse palmoplantar keratoderma as a major feature
MONDO:0015008	amelogenesis imperfecta, type 1J
MONDO:0017662	miscellaneous movement disorder due to genetic neurodegenerative disease
MONDO:0017663	inherited tremor disorder
MONDO:0017664	rare genetic myoclonus
MONDO:0017665	rare genetic disease with myoclonus as a major feature
MONDO:0015003	dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities
MONDO:0015002	developmental and epileptic encephalopathy, 49
MONDO:0017660	rare genetic parkinsonian disorder
MONDO:0015001	atrial fibrillation, familial, 18
MONDO:0017661	rare parkinsonian syndrome due to genetic neurodegenerative disease
MONDO:0015000	developmental and epileptic encephalopathy, 48
MONDO:0003007	childhood kidney cell carcinoma
MONDO:0054637	Noonan syndrome-like disorder with loose anagen hair 1
MONDO:0003008	hereditary renal cell carcinoma
MONDO:0054636	Skraban-Deardorff syndrome
MONDO:0005669	black piedra
MONDO:0003009	hyperaldosteronism
MONDO:0003003	cervical alveolar soft part sarcoma
MONDO:0005666	berylliosis
MONDO:0005665	Bell's palsy
MONDO:0003004	macular degeneration
MONDO:0005668	bird fancier's lung
MONDO:0003005	macular retinal edema
MONDO:0005667	biliary dyskinesia
MONDO:0003006	Bartter disease
MONDO:0005662	balantidiasis
MONDO:0005661	babesiosis
MONDO:0003000	central nervous system germ cell tumor
MONDO:0005664	bartonellosis
MONDO:0003001	seminoma
MONDO:0005663	Barre-Lieou syndrome
MONDO:0003002	dysgerminoma
MONDO:0005660	Avulavirus infectious disease
MONDO:0017659	sporadic hyperekplexia
MONDO:0017655	progressive epilepsy and/or ataxia with myoclonus as a major feature
MONDO:0017656	motor stereotypies
MONDO:0017657	rare paroxysmal movement disorder
MONDO:0017658	hyperekplexia
MONDO:0017651	primary myoclonus
MONDO:0017652	rare disease with myoclonus as a major feature
MONDO:0017653	epilepsy and/or ataxia with myoclonus as major feature
MONDO:0017654	non progressive epilepsy and/or ataxia with myoclonus as a major feature
MONDO:0017650	rare myoclonus
MONDO:0003018	myotonic disease
MONDO:0003019	potassium deficiency disease
MONDO:0003014	rhinitis
MONDO:0005677	Rickettsia conorii infectious disease
MONDO:0005676	borna disease
MONDO:0003015	malignant biphasic mesothelioma
MONDO:0005679	bovine virus diarrhea-mucosal disease
MONDO:0003016	sarcomatoid mesothelioma
MONDO:0003017	malignant peritoneal solitary fibrous tumor
MONDO:0005678	bovine respiratory disease complex
MONDO:0005673	blind loop syndrome
MONDO:0003010	multilocular clear cell renal cell carcinoma
MONDO:0003011	mucinous tubular and spindle renal cell carcinoma
MONDO:0005672	blastomycosis
MONDO:0003012	sarcomatoid renal cell carcinoma
MONDO:0005675	border disease
MONDO:0005674	bone giant cell tumor
MONDO:0003013	pseudohypoaldosteronism
MONDO:0005671	Blastocystis infectious disease
MONDO:0005670	blackwater fever
MONDO:0017648	Sydenham chorea
MONDO:0017649	hemidystonia-hemiatrophy syndrome
MONDO:0017644	rare tremor disorder
MONDO:0017645	rare choreic movement disorder
MONDO:0017646	neurodegenerative disease with chorea
MONDO:0017647	postinfectious autoimmune disease with chorea
MONDO:0017640	cyanide-induced parkinsonism
MONDO:0017641	miscellaneous movement disorder due to neurodegenerative disease
MONDO:0017642	intellectual disability-microcephaly-phalangeal-facial abnormalities syndrome
MONDO:0017643	frontotemporal neurodegeneration with movement disorder
MONDO:0030604	cystic partially differentiated nephroblastoma
MONDO:0030603	Klebsiella infectious disease
MONDO:0015050	esophageal duplication cyst
MONDO:0003069	suppurative lymphadenitis
MONDO:0030602	Klebsiella pneumonia
MONDO:0003065	nasal cavity inverting papilloma
MONDO:0003066	submandibular adenitis
MONDO:0003067	cervical lymphadenitis
MONDO:0003068	postauricular lymphadenitis
MONDO:0003061	benign muscle neoplasm
MONDO:0003062	intestinal benign neoplasm
MONDO:0003063	hydranencephaly
MONDO:0003064	inverted transitional cell papilloma
MONDO:0003060	biliary tract cancer
MONDO:0015059	progressive non-fluent aphasia
MONDO:0015054	hereditary angioedema type 2
MONDO:0015053	hereditary angioedema type 1
MONDO:0015052	primary interstitial lung disease specific to childhood due to pulmonary surfactant protein anomalies
MONDO:0015051	tubular duplication of the esophagus
MONDO:0015058	Waterhouse-Friderichsen syndrome
MONDO:0015057	renin-angiotensin-aldosterone system-blocker-induced angioedema
MONDO:0015056	acquired angioedema type 1
MONDO:0015055	acquired angioedema type 2
MONDO:0027029	HHV-6 encephalitis
MONDO:0003076	unilateral retinoblastoma
MONDO:0003077	intraocular retinoblastoma
MONDO:0003078	extraocular retinoblastoma
MONDO:0003079	mastocytoma
MONDO:0003072	retinal cancer
MONDO:0027026	Buschke Lowenstein tumor
MONDO:0003073	trilateral retinoblastoma
MONDO:0003074	familial retinoblastoma
MONDO:0003075	bilateral retinoblastoma
MONDO:0015049	solitary necrotic nodule of the liver
MONDO:0003070	axillary lymphadenitis
MONDO:0015048	amelogenesis imperfecta type 2
MONDO:0003071	epidermolysis bullosa simplex
MONDO:0015043	extramedullary soft tissue plasmacytoma
MONDO:0015042	primary plasmacytoma of the bone
MONDO:0015041	myelodysplastic syndrome with excess blasts-2
MONDO:0015040	myelodysplastic syndrome with excess blasts-1
MONDO:0015047	amelogenesis imperfecta type 1
MONDO:0015046	gamma-heavy chain disease
MONDO:0015045	alpha-heavy chain disease
MONDO:0015044	mu-heavy chain disease
MONDO:0017690	disorder of galactose metabolism
MONDO:0003047	thymic large cell neuroendocrine carcinoma
MONDO:0003048	type C thymoma
MONDO:0003049	ovarian large-cell neuroendocrine carcinoma
MONDO:0003043	extraskeletal mesenchymal chondrosarcoma
MONDO:0003044	extraosseous chondrosarcoma
MONDO:0003045	anal gland neoplasm
MONDO:0003046	anus neoplasm
MONDO:0003040	retrograde amnesia
MONDO:0003041	pediatric mesenchymal chondrosarcoma
MONDO:0003042	adult mesenchymal chondrosarcoma
MONDO:0042604	Sandhaus-Ben-Ami syndrome
MONDO:0015039	lissencephaly with cerebellar hypoplasia type F
MONDO:0042605	Y chromosome infertility due to DAZ1 deletion
MONDO:0015038	lissencephaly with cerebellar hypoplasia type E
MONDO:0015037	lissencephaly with cerebellar hypoplasia type D
MONDO:0017699	glycogen storage disease due to glycogen branching enzyme deficiency, childhood combined hepatic and myopathic form
MONDO:0042600	Sammartino-Decreccio syndrome
MONDO:0042601	Samson-Gardner syndrome
MONDO:0042602	Samson-Viljoen syndrome
MONDO:0042603	Sanderson-Fraser syndrome
MONDO:0017695	glycogen storage disease due to glycogen branching enzyme deficiency, progressive hepatic form
MONDO:0015032	intraneural perineurioma
MONDO:0017696	glycogen storage disease due to glycogen branching enzyme deficiency, non progressive hepatic form
MONDO:0015031	extraneural perineurioma
MONDO:0017697	glycogen storage disease due to glycogen branching enzyme deficiency, fatal perinatal neuromuscular form
MONDO:0015030	sclerosing perineurioma
MONDO:0017698	glycogen storage disease due to glycogen branching enzyme deficiency, congenital neuromuscular form
MONDO:0015036	lissencephaly with cerebellar hypoplasia type C
MONDO:0017691	erythrocyte galactose epimerase deficiency
MONDO:0015035	lissencephaly with cerebellar hypoplasia type B
MONDO:0017692	generalized galactose epimerase deficiency
MONDO:0017693	glycogen storage disease due to glycogen synthase deficiency
MONDO:0015034	lissencephaly with cerebellar hypoplasia type A
MONDO:0017694	glycogen storage disease due to acid maltase deficiency, infantile onset
MONDO:0015033	ABeta amyloidosis, dutch type
MONDO:0003058	microcystic meningioma
MONDO:0003059	bile duct cancer
MONDO:0003054	benign meningioma
MONDO:0003055	secretory meningioma
MONDO:0003056	lymphoplasmacyte-rich meningioma
MONDO:0003057	pediatric meningioma
MONDO:0003050	lung large cell carcinoma
MONDO:0003051	non specific chronic endometritis
MONDO:0003052	granulomatous endometritis
MONDO:0003053	choroid plexus meningioma
MONDO:0015029	reticular perineurioma
MONDO:0015028	48,XXYY syndrome
MONDO:0015027	familial isolated hyperparathyroidism
MONDO:0015026	cerebroretinal microangiopathy with calcifications and cysts 2
MONDO:0017688	disorder of glycolysis
MONDO:0017689	disorder of fructose metabolism
MONDO:0017684	disorder of beta and omega amino acid metabolism
MONDO:0015021	hypotonia, ataxia, and delayed development syndrome
MONDO:0015020	intellectual disability, autosomal recessive 59
MONDO:0017685	vitamin B12-responsive methylmalonic acidemia, type cblDv2
MONDO:0017686	inborn aminoacylase deficiency
MONDO:0017687	disorder of neutral amino acid transport
MONDO:0015025	developmental and epileptic encephalopathy, 51
MONDO:0017680	autosomal recessive disease associated with punctate palmoplantar keratoderma as a major feature
MONDO:0017681	erythrokeratoderma variabilis progressiva
MONDO:0015024	ectodermal dysplasia 12, hypohidrotic/hair/tooth/nail type
MONDO:0015023	MYPN-related myopathy
MONDO:0017682	intellectual disability-polydactyly-uncombable hair syndrome
MONDO:0015022	intellectual developmental disorder with dysmorphic facies and ptosis
MONDO:0017683	methylcobalamin deficiency type cblDv1
MONDO:0005604	plasma cell leukemia
MONDO:0005603	pancreatic tubular adenocarcinoma
MONDO:0005606	tubular adenocarcinoma
MONDO:0005605	transitional cell papilloma
MONDO:0005600	ovarian adenocarcinoma
MONDO:0005602	ovarian teratoma
MONDO:0005601	ovarian mucinous adenocarcinoma
MONDO:0005615	plasmacytoma
MONDO:0005614	pancreatic adenosquamous carcinoma
MONDO:0005617	undifferentiated carcinoma
MONDO:0005616	pulmonary mucoepidermoid carcinoma
MONDO:0005611	bladder transitional cell carcinoma
MONDO:0005610	Kashin-Beck disease
MONDO:0005613	mesonephric adenocarcinoma
MONDO:0005612	ovarian leiomyosarcoma
MONDO:0005608	varicella zoster infection
MONDO:0005607	chronic bronchitis
MONDO:0005609	herpes zoster
MONDO:0005648	aortic valve insufficiency
MONDO:0005647	anogenital human papillomavirus infection
MONDO:0005649	appendicitis
MONDO:0005644	amebiasis
MONDO:0005643	Alphavirus infectious disease
MONDO:0005646	anisakiasis
MONDO:0005645	ancylostomiasis
MONDO:0005640	akinetic mutism
MONDO:0005642	atopic conjunctivitis
MONDO:0005641	aleutian mink disease
MONDO:0017637	rare parkinsonian syndrome due to intoxication
MONDO:0017638	manganese poisoning
MONDO:0017639	carbon monoxide-induced parkinsonism
MONDO:0017633	rare intoxication due to medical products
MONDO:0017634	non-infectious anterior uveitis
MONDO:0017635	parkinsonian syndrome due to neurodegenerative disease
MONDO:0017636	hemiparkinsonism-hemiatrophy syndrome
MONDO:0017630	X-linked complicated spastic paraplegia type 1
MONDO:0017631	rare tumor of gallbladder and extrahepatic biliary tract
MONDO:0017632	rare tumor of liver and intrahepatic biliary tract
MONDO:0005659	atrophic rhinitis
MONDO:0005658	Astroviridae infectious disease
MONDO:0005655	ascaridiasis
MONDO:0005654	ascariasis
MONDO:0005657	aspergillosis
MONDO:0005656	Ascaridida infectious disease
MONDO:0005651	arenavirus hemorrhagic fever
MONDO:0005650	Arenaviridae infectious disease
MONDO:0005653	asbestosis
MONDO:0005652	Arterivirus infectious disease
MONDO:0017619	congenital sucrase-isomaltase deficiency with minimal starch tolerance
MONDO:0017626	familial primary hypomagnesemia with normocalcuria
MONDO:0017627	congenital hereditary facial paralysis-variable hearing loss syndrome
MONDO:0017628	myospherulosis
MONDO:0017629	sodium channelopathy-related small fiber neuropathy
MONDO:0017622	congenital sucrase-isomaltase deficiency without sucrose intolerance
MONDO:0017623	PTEN hamartoma tumor syndrome
MONDO:0017624	familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis
MONDO:0017625	familial primary hypomagnesemia with hypocalcuria
MONDO:0017620	congenital sucrase-isomaltase deficiency without starch intolerance
MONDO:0017621	congenital sucrase-isomaltase deficiency with starch and lactose intolerance
MONDO:0005626	epithelial neoplasm
MONDO:0005625	cerebral malaria
MONDO:0005628	male breast carcinoma
MONDO:0005627	head and neck cancer
MONDO:0005622	vasculitis
MONDO:0005621	vascular brain injury
MONDO:0005624	atrophic thyroiditis
MONDO:0005623	autoimmune thyroid disease
MONDO:0005620	cerebral amyloid angiopathy
MONDO:0017608	dystrophic epidermolysis bullosa
MONDO:0017609	renal tubular dysgenesis
MONDO:0017615	benign familial infantile epilepsy
MONDO:0017616	X-linked intellectual disability, Schutz type
MONDO:0017617	acquired adult-onset immunodeficiency
MONDO:0017618	congenital sucrase-isomaltase deficiency with starch intolerance
MONDO:0017611	pituitary tumor
MONDO:0017612	junctional epidermolysis bullosa
MONDO:0017613	intellectual disability-hypotonia-skin hyperpigmentation syndrome
MONDO:0017614	X-linked intellectual disability-hypogonadism-ichthyosis-obesity-short stature syndrome
MONDO:0017610	epidermolysis bullosa simplex
MONDO:0005619	typhoid fever
MONDO:0005618	anxiety disorder
MONDO:0005637	adult-onset Still disease
MONDO:0005636	adenosarcoma
MONDO:0005639	AIDS related complex
MONDO:0005638	agnosia
MONDO:0005633	acute disseminated encephalomyelitis
MONDO:0005632	acute chest syndrome
MONDO:0005635	adenomyoma
MONDO:0005634	acute hemorrhagic conjunctivitis
MONDO:0005631	actinomycosis
MONDO:0005630	actinobacillosis
MONDO:0017604	marginal zone lymphoma
MONDO:0017605	ependymal tumor
MONDO:0017606	facial nerve palsy due to herpes zoster infection
MONDO:0017607	caudal regression sequence
MONDO:0017600	hairy cell leukemia variant
MONDO:0017601	diffuse large B-cell lymphoma with chronic inflammation
MONDO:0017602	ALK-positive anaplastic large cell lymphoma
MONDO:0017603	ALK-negative anaplastic large cell lymphoma
MONDO:0005629	Acanthamoeba keratitis
MONDO:0042486	polyposis syndrome, hereditary mixed, 1
MONDO:0042487	uterine cervix carcinoma in situ
MONDO:0042488	Cestode infectious disease
MONDO:0042489	disease susceptibility
MONDO:0042484	disseminated sporotrichosis
MONDO:0042485	infective arthritis
MONDO:0042490	neutropenia, severe congenital, 1, autosomal dominant
MONDO:0017490	tibial hemimelia, unilateral
MONDO:0017491	tibial hemimelia, bilateral
MONDO:0042491	cervical squamous intraepithelial neoplasia
MONDO:0017492	fibular hemimelia, unilateral
MONDO:0042497	mycotoxicosis
MONDO:0042498	Ruzicka-Goerz-Anton syndrome
MONDO:0042499	benign familial neonatal-infantile seizures 1
MONDO:0042493	gastric non-hodgkin lymphoma
MONDO:0042494	childhood malignant melanoma
MONDO:0042495	arteriosclerotic retinopathy
MONDO:0042496	ergotism
MONDO:0017497	congenital absence of thigh and lower leg with foot present, bilateral
MONDO:0017498	congenital absence of both forearm and hand, unilateral
MONDO:0017499	congenital absence of both forearm and hand, bilateral
MONDO:0017493	fibular hemimelia, bilateral
MONDO:0017494	congenital absence of upper arm and forearm with hand present, unilateral
MONDO:0017495	congenital absence of upper arm and forearm with hand present, bilateral
MONDO:0017496	congenital absence of thigh and lower leg with foot present, unilateral
MONDO:0017480	amelia of lower limb, unilateral
MONDO:0017481	amelia of lower limb, bilateral
MONDO:0017486	radial hemimelia, unilateral
MONDO:0017487	radial hemimelia, bilateral
MONDO:0017488	ulnar hemimelia, bilateral
MONDO:0017489	ulnar hemimelia, unilateral
MONDO:0017482	humeral agenesis/hypoplasia, unilateral
MONDO:0017483	humeral agenesis/hypoplasia, bilateral
MONDO:0017484	femoral agenesis/hypoplasia, unilateral
MONDO:0017485	femoral agenesis/hypoplasia, bilateral
MONDO:0042433	mycotic endocarditis
MONDO:0042451	endomyometritis
MONDO:0042452	tertiary lesion of yaws
MONDO:0042458	Trichinella spiralis infectious disease
MONDO:0005567	substance withdrawal syndrome
MONDO:0005566	neonatal abstinence syndrome
MONDO:0005569	cartilage disease
MONDO:0005568	cholesterol embolism
MONDO:0005563	nut midline carcinoma
MONDO:0005562	age-related hearing impairment
MONDO:0005565	blastoma
MONDO:0005564	embryonal neoplasm
MONDO:0005561	aortic disease
MONDO:0005560	brain disease
MONDO:0017556	Madelung deformity, unilateral
MONDO:0017557	Madelung deformity, bilateral
MONDO:0017558	congenital elbow dislocation, unilateral
MONDO:0017559	congenital elbow dislocation, bilateral
MONDO:0017552	humero-ulnar synostosis, unilateral
MONDO:0017553	humero-ulnar synostosis, bilateral
MONDO:0017554	radio-ulnar synostosis, unilateral
MONDO:0017555	radio-ulnar synostosis, bilateral
MONDO:0017550	humero-radial synostosis, unilateral
MONDO:0017551	humero-radial synostosis, bilateral
MONDO:0005578	arthritic joint disease
MONDO:0005577	narcolepsy without cataplexy
MONDO:0005579	epilepsy, idiopathic generalized
MONDO:0005574	tauopathy
MONDO:0005573	type II hypersensitivity reaction disease
MONDO:0005576	cryoglobulinemia
MONDO:0005575	colorectal cancer
MONDO:0005570	hematologic disease
MONDO:0005572	polycythemia due to hypoxia
MONDO:0005571	polycythemia
MONDO:0017549	humero-radio-ulnar synostosis, bilateral
MONDO:0017545	zygodactyly type 4
MONDO:0017546	congenital vertical talus, unilateral
MONDO:0017547	congenital vertical talus, bilateral
MONDO:0017548	humero-radio-ulnar synostosis, unilateral
MONDO:0017541	central polydactyly of toes, unilateral
MONDO:0017542	central polydactyly of toes, bilateral
MONDO:0017543	zygodactyly type 2
MONDO:0017544	zygodactyly type 3
MONDO:0017540	postaxial polydactyly of toes, bilateral
MONDO:0005549	renal cell adenocarcinoma
MONDO:0005548	malignant rhabdoid tumour
MONDO:0005545	staphylococcus aureus infection
MONDO:0005544	hippocampal sclerosis of aging
MONDO:0005547	desmoplastic medulloblastoma
MONDO:0005546	fibromyalgia
MONDO:0005541	spondylolysis
MONDO:0005540	rectal adenocarcinoma
MONDO:0005543	autoimmune hepatitis type 1
MONDO:0005542	acute coronary syndrome
MONDO:0017538	Preaxial polydactyly of toes, bilateral
MONDO:0017539	postaxial polydactyly of toes, unilateral
MONDO:0017534	postaxial polydactyly type B, bilateral
MONDO:0017535	central polydactyly of fingers, unilateral
MONDO:0017536	central polydactyly of fingers, bilateral
MONDO:0017537	Preaxial polydactyly of toes, unilateral
MONDO:0017530	polysyndactyly, bilateral
MONDO:0017531	postaxial polydactyly type A, unilateral
MONDO:0017532	postaxial polydactyly type A, bilateral
MONDO:0017533	postaxial polydactyly type B, unilateral
MONDO:0005559	neurodegenerative disease
MONDO:0005556	lupus nephritis
MONDO:0005555	cycloplegia
MONDO:0005558	ovarian disease
MONDO:0005557	calcium metabolic disease
MONDO:0005552	ocular vascular disease
MONDO:0005551	eye allergy
MONDO:0005554	rheumatic disorder
MONDO:0005553	parathyroid disease
MONDO:0005550	infectious disease
MONDO:0017527	polydactyly of an index finger, unilateral
MONDO:0017528	polydactyly of an index finger, bilateral
MONDO:0017529	polysyndactyly, unilateral
MONDO:0017523	polydactyly of a biphalangeal thumb, unilateral
MONDO:0017524	polydactyly of a biphalangeal thumb, bilateral
MONDO:0017525	polydactyly of a triphalangeal thumb, unilateral
MONDO:0017526	polydactyly of a triphalangeal thumb, bilateral
MONDO:0017520	symbrachydactyly of hand and foot, bilateral
MONDO:0017521	hyperphalangy, unilateral
MONDO:0017522	hyperphalangy, bilateral
MONDO:0017590	carcinoma of the ampulla of vater
MONDO:0017591	combined pulmonary fibrosis-emphysema syndrome
MONDO:0017596	diffuse large B-cell lymphoma of the central nervous system
MONDO:0017597	T-cell/histiocyte rich large B cell lymphoma
MONDO:0017598	primary cutaneous anaplastic large cell lymphoma
MONDO:0017599	splenic diffuse red pulp small B-cell lymphoma
MONDO:0017592	staphylococcal toxemia
MONDO:0017593	juvenile amyotrophic lateral sclerosis
MONDO:0017594	indolent B-cell non-Hodgkin lymphoma
MONDO:0017595	aggressive B-cell non-Hodgkin lymphoma
MONDO:0017580	11p15.4 microduplication syndrome
MONDO:0017589	follicular cholangitis and pancreatitis
MONDO:0017585	painful orbital and systemic neurofibromas-marfanoid habitus syndrome
MONDO:0017586	onychocytic matricoma
MONDO:0017587	onychomatricoma
MONDO:0017588	nail tumor
MONDO:0017581	familial infantile gigantism
MONDO:0017582	pituitary adenocarcinoma
MONDO:0017583	mirror polydactyly-vertebral segmentation-limbs defects syndrome
MONDO:0017584	Sagliker syndrome
MONDO:0005589	thiopurine immunosuppressant-induced pancreatitis
MONDO:0005588	chemotherapy-induced oral mucositis
MONDO:0030502	tetrasomy
MONDO:0005585	chemotherapy-induced hypertension
MONDO:0005584	congenital left-sided heart lesions
MONDO:0005587	non-Hodgkins lymphoma
MONDO:0005586	head and neck neoplasm
MONDO:0005581	AVL induced bursal lymphoma
MONDO:0005580	esophageal squamous cell carcinoma
MONDO:0005583	non-human animal disease
MONDO:0005582	binge eating disorder
MONDO:0017578	disorder of thiamine metabolism and transport
MONDO:0017579	Baraitser-Winter cerebrofrontofacial syndrome
MONDO:0017574	chronic intestinal pseudoobstruction
MONDO:0017575	mitochondrial neurogastrointestinal encephalomyopathy
MONDO:0017576	46,XX disorder of sex development
MONDO:0017577	spontaneous periodic hypothermia
MONDO:0017570	leukocyte adhesion deficiency
MONDO:0017571	Proteus-like syndrome
MONDO:0017572	tick-borne encephalitis
MONDO:0017573	46,XX disorder of sex development-anorectal anomalies syndrome
MONDO:0005599	malignant epithelioid mesothelioma
MONDO:0005596	cystadenocarcinoma
MONDO:0005595	laryngeal squamous cell carcinoma
MONDO:0005598	dopaminergic neuroblastoma
MONDO:0005597	cystic renal cell carcinoma
MONDO:0005592	smooth surface dental caries
MONDO:0005591	pit and fissure surface dental caries
MONDO:0005594	severe cutaneous adverse reaction
MONDO:0005593	chronic periodontitis
MONDO:0005590	breast ductal adenocarcinoma
MONDO:0017567	macrodactyly of toes, bilateral
MONDO:0017568	Prata-Liberal-Goncalves syndrome
MONDO:0017569	de Barsy syndrome
MONDO:0017563	congenital patella dislocation, bilateral
MONDO:0017564	macrodactyly of fingers, unilateral
MONDO:0017565	macrodactyly of fingers, bilateral
MONDO:0017566	macrodactyly of toes, unilateral
MONDO:0017560	congenital genu recurvatum
MONDO:0017561	congenital genu flexum
MONDO:0017562	congenital patella dislocation, unilateral
MONDO:0005527	toxic encephalopathy
MONDO:0005526	tetanus
MONDO:0005529	methylmalonic aciduria and homocystinuria type cblG
MONDO:0005528	inborn vitamin metabolic disorder
MONDO:0005523	steroid inherited metabolic disorder
MONDO:0005522	small intestine carcinoma
MONDO:0005525	T-cell leukemia
MONDO:0005524	sweat gland carcinoma
MONDO:0005521	shigellosis
MONDO:0005520	rickets
MONDO:0017509	adactyly of foot, unilateral
MONDO:0017516	brachydactyly of fingers, bilateral
MONDO:0017517	brachydactyly of toes, unilateral
MONDO:0017518	brachydactyly of toes, bilateral
MONDO:0017519	symbrachydactyly of hand and foot, unilateral
MONDO:0017512	split hand, bilateral
MONDO:0017513	split foot, unilateral
MONDO:0017514	split foot, bilateral
MONDO:0017515	brachydactyly of fingers, unilateral
MONDO:0017510	adactyly of foot, bilateral
MONDO:0017511	split hand, unilateral
MONDO:0005519	renal pelvis carcinoma
MONDO:0005538	proctitis
MONDO:0005537	perianal Crohn disease
MONDO:0005539	small bowel Crohn disease
MONDO:0005534	ileocolitis
MONDO:0005533	distal colitis
MONDO:0005536	pancolitis
MONDO:0005535	oral Crohn disease
MONDO:0005530	opiate dependence
MONDO:0005532	Crohn's colitis
MONDO:0005531	morphine dependence
MONDO:0017505	apodia, bilateral
MONDO:0017506	congenital absence/hypoplasia of thumb, unilateral
MONDO:0017507	congenital absence/hypoplasia of thumb, bilateral
MONDO:0017508	congenital absence/hypoplasia of fingers excluding thumb, bilateral
MONDO:0017501	congenital absence of both lower leg and foot, bilateral
MONDO:0017502	acheiria, unilateral
MONDO:0017503	acheiria, bilateral
MONDO:0017504	apodia, unilateral
MONDO:0017500	congenital absence of both lower leg and foot, unilateral
MONDO:0005505	dysembryoplastic neuroepithelial tumor
MONDO:0005504	diphtheria
MONDO:0005507	gingival cancer
MONDO:0005506	eccrine sweat gland cancer
MONDO:0005501	congenital disorder of glycosylation type II
MONDO:0005500	congenital disorder of glycosylation type I
MONDO:0005503	developmental disorder of mental health
MONDO:0005502	dengue disease
MONDO:0005516	osteochondrodysplasia
MONDO:0005515	oral cavity cancer
MONDO:0005518	pseudohermaphroditism
MONDO:0005517	pharynx cancer
MONDO:0005512	malignant peritoneal mesothelioma
MONDO:0005511	janus kinase-3 deficiency
MONDO:0005514	nanophthalmia
MONDO:0005513	methylmalonic aciduria and homocystinuria type cblE
MONDO:0005510	hydronephrosis
MONDO:0005509	histiocytoma
MONDO:0005508	hereditary multiple osteochondromas
MONDO:0017390	methylmalonic acidemia without homocystinuria
MONDO:0017391	Grayson-Wilbrandt corneal dystrophy
MONDO:0017392	pre-descemet corneal dystrophy
MONDO:0017393	blepharophimosis - intellectual disability syndrome
MONDO:0017398	3MC syndrome
MONDO:0017399	frontotemporal dementia, right temporal atrophy variant
MONDO:0017394	ketamine-induced biliary dilatation
MONDO:0017395	fixed pigmented erythema
MONDO:0017396	toxic dermatosis
MONDO:0017397	constitutional dyserythropoietic anemia
MONDO:0017380	juvenile polyposis syndrome
MONDO:0017381	congenital herpes simplex virus infection
MONDO:0017382	familial clubfoot due to 5q31 microdeletion
MONDO:0017387	epithelioid sarcoma
MONDO:0017388	celiac trunk compression syndrome
MONDO:0017389	tetrahydrobiopterin-responsive hyperphenylalaninemia/phenylketonuria
MONDO:0017383	familial clubfoot due to PITX1 point mutation
MONDO:0017384	acute generalized exanthematous pustulosis
MONDO:0017385	malignant migrating partial seizures of infancy
MONDO:0017386	pleomorphic rhabdomyosarcoma
MONDO:0042370	Yersinia enterocolitica infectious disease
MONDO:0017370	autoinflammatory syndrome with skin involvement
MONDO:0017371	rare head and neck tumor
MONDO:0005387	primary ovarian failure
MONDO:0005386	peripheral arterial disease
MONDO:0005389	sclerosing cholangitis
MONDO:0005388	primary biliary cholangitis
MONDO:0005383	panic disorder
MONDO:0005382	bone Paget disease
MONDO:0005385	vascular disease
MONDO:0005384	partial epilepsy
MONDO:0005381	bone disease
MONDO:0005380	osteonecrosis
MONDO:0017376	reactive arthritis
MONDO:0017377	preaxial polydactyly-colobomata-intellectual disability syndrome
MONDO:0017378	polymicrogyria-turricephaly-hypogenitalism syndrome
MONDO:0017379	polyneuropathy-intellectual disability-acromicria-premature menopause syndrome
MONDO:0017372	congenital varicella syndrome
MONDO:0017373	poliomyelitis
MONDO:0017374	polydactyly
MONDO:0017375	congenital enterovirus infection
MONDO:0017360	vitamin B12-unresponsive methylmalonic acidemia type mut0
MONDO:0005398	upper aerodigestive tract neoplasm
MONDO:0005397	goiter
MONDO:0005399	venous thromboembolism
MONDO:0005394	brain infarction
MONDO:0005393	gout
MONDO:0005396	thoracic aortic aneurysm
MONDO:0005395	movement disorder
MONDO:0005390	cardiac arrhythmia
MONDO:0005392	scoliosis
MONDO:0005391	restless legs syndrome
MONDO:0017369	autoinflammatory syndrome with immune deficiency
MONDO:0017365	hereditary acrokeratotic poikiloderma, Weary type
MONDO:0017366	hereditary pheochromocytoma-paraganglioma
MONDO:0017367	kindler syndrome
MONDO:0017368	systemic disease with skin involvement
MONDO:0017361	congenital rubella syndrome
MONDO:0017362	neuralgic amyotrophy
MONDO:0017363	idiopathic chronic eosinophilic pneumonia
MONDO:0017364	POEMS syndrome
MONDO:0030329	megacystis-microcolon-intestinal hypoperistalsis syndrome 5
MONDO:0030326	mitochondrial dna depletion syndrome 16B (neuroophthalmic type)
MONDO:0044972	eosinophil disease
MONDO:0044975	disease of transporter activity
MONDO:0044974	disease of supramolecular complex
MONDO:0044971	disease of macromolecular complex
MONDO:0044970	mitochondrial disease
MONDO:0044969	disease of membrane bound organelle
MONDO:0044965	abdominal and pelvic region disorder
MONDO:0044967	limb disorder
MONDO:0030332	ciliary dyskinesia, primary, 46
MONDO:0030331	Ritscher-Schinzel syndrome 4
MONDO:0030334	encephalitis, acute, infection (viral)-induced, susceptibility to, 11
MONDO:0030333	immunodeficiency 84
MONDO:0030330	cardiomyopathy, familial restrictive, 6
MONDO:0030339	microcephaly 28, primary, autosomal recessive
MONDO:0030335	diarrhea 12, with microvillus atrophy
MONDO:0030338	anencephaly 2
MONDO:0030337	cutis laxa, autosomal recessive, type 2E
MONDO:0044984	nasolacrimal duct disease
MONDO:0044983	benign lipomatous neoplasm
MONDO:0044986	lymphoid system disease
MONDO:0044980	disease of signal transduction
MONDO:0044982	drug pseudoallergy
MONDO:0044981	pseudoallergy
MONDO:0044977	disease of receptor activity
MONDO:0044976	disease of catalytic activity
MONDO:0044979	disease by cell type
MONDO:0044978	disease of cell nucleus
MONDO:0030341	myasthenic syndrome, congenital, 7B, presynaptic, autosomal recessive
MONDO:0030346	ciliary dyskinesia, primary, 47, and lissencephaly
MONDO:0044995	parasympathetic nervous system disease
MONDO:0044997	midbrain disease
MONDO:0044996	cerebral cortex disease
MONDO:0044991	upper digestive tract disease
MONDO:0044990	hand disease
MONDO:0044993	sympathetic nervous system disease
MONDO:0044992	mouth mucosa disease
MONDO:0044988	hip region disease
MONDO:0044987	face disease
MONDO:0044989	foot disease
MONDO:0030354	facioscapulohumeral muscular dystrophy 3, digenic
MONDO:0030353	Joubert syndrome 38
MONDO:0030356	short-rib thoracic dysplasia 21 without polydactyly
MONDO:0030355	facioscapulohumeral muscular dystrophy 4, digenic
MONDO:0044999	scalp disease
MONDO:0044998	carpal region disease
MONDO:0030366	cardiomyopathy, dilated, 2E
MONDO:0030361	Aicardi-Goutieres syndrome 8
MONDO:0030360	cholestasis, progressive familial intrahepatic, 6
MONDO:0030362	Aicardi-Goutieres syndrome 9
MONDO:0005449	conduction system disorder
MONDO:0005446	cutaneous leishmaniasis
MONDO:0005445	visceral leishmaniasis
MONDO:0005448	hepatitis C induced liver cirrhosis
MONDO:0005447	testicular cancer
MONDO:0005442	type 1 diabetes nephropathy
MONDO:0005441	otitis media
MONDO:0005444	leishmaniasis
MONDO:0005443	type 2 diabetes nephropathy
MONDO:0005440	embryonal carcinoma
MONDO:0017439	tetra-amelia
MONDO:0017435	popliteal pterygium syndrome
MONDO:0017436	lethal congenital contracture syndrome
MONDO:0017437	amelia of upper limb
MONDO:0017438	amelia of lower limb
MONDO:0017431	non-syndromic limb overgrowth
MONDO:0017432	syndrome with limb reduction defects
MONDO:0017433	dysostosis with combined reduction defects of upper and lower limbs
MONDO:0017434	syndrome with limb duplication, polydactyly, syndactyly, and/or hyperphalangy
MONDO:0017430	non-syndromic congenital joint dislocations
MONDO:0005457	acute stress reaction
MONDO:0005456	avian influenza
MONDO:0005459	human African trypanosomiasis
MONDO:0005458	q fever
MONDO:0005453	congenital heart disease
MONDO:0005452	bulimia nervosa
MONDO:0005455	cholangiocarcinoma
MONDO:0005454	lung neuroendocrine neoplasm
MONDO:0005451	eating disorder
MONDO:0005450	autoimmune disease
MONDO:0017428	congenital deformities of fingers
MONDO:0017429	joint formation defects
MONDO:0017424	non-syndromic brachydactyly
MONDO:0017425	preaxial polydactyly of fingers
MONDO:0017426	postaxial polydactyly of fingers
MONDO:0017427	congenital deformities of limbs
MONDO:0017420	intercalary limb defects
MONDO:0017421	non-syndromic terminal limb defects
MONDO:0017422	adactyly of hand
MONDO:0017423	split hand or/and split foot malformation
MONDO:0005428	pemphigus vulgaris
MONDO:0005427	vasuclar dementia
MONDO:0005429	prion disease
MONDO:0005424	elephantiasis
MONDO:0005423	pelvic organ prolapse
MONDO:0005426	MRI defined brain infarct
MONDO:0005425	podoconiosis
MONDO:0005420	hypothyroidism
MONDO:0005422	nodular sclerosis Hodgkin lymphoma
MONDO:0005421	infantile hypertrophic pyloric stenosis
MONDO:0017417	renal-hepatic-pancreatic dysplasia
MONDO:0017418	chronic intestinal failure
MONDO:0017419	non-syndromic amelia
MONDO:0017413	Reunion island Larsen syndrome
MONDO:0017414	rare nevus
MONDO:0017415	multiple pterygium syndrome
MONDO:0017416	postpoliomyelitis syndrome
MONDO:0017410	porencephaly
MONDO:0017411	neonatal inflammatory skin and bowel disease
MONDO:0017412	2q31.1 microduplication syndrome
MONDO:0005439	familial hypercholesterolemia
MONDO:0005438	metastatic malignant neoplasm in the lymph nodes
MONDO:0005435	anti-neutrophil antibody associated vasculitis
MONDO:0005434	skin sensitivity to sun
MONDO:0005437	testicular dysgenesis syndrome
MONDO:0005436	postoperative ventricular dysfunction
MONDO:0005431	toxic epidermal necrolysis
MONDO:0005430	early onset hypertension
MONDO:0005433	alcohol withdrawal
MONDO:0005432	alcohol and nicotine codependence
MONDO:0017406	hypogonadotropic hypogonadism-severe microcephaly-sensorineural hearing loss-dysmorphism syndrome
MONDO:0017407	deficiency in anterior pituitary function - variable immunodeficiency syndrome
MONDO:0017408	rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome
MONDO:0017409	fetal cytomegalovirus syndrome
MONDO:0017402	familial isolated arrhythmogenic ventricular dysplasia, biventricular form
MONDO:0017403	familial isolated arrhythmogenic ventricular dysplasia, right dominant form
MONDO:0017404	distal Xq28 microduplication syndrome
MONDO:0017405	1p21.3 microdeletion syndrome
MONDO:0017400	hypoplastic pancreas-intestinal atresia-hypoplastic gallbalder syndrome
MONDO:0017401	familial isolated arrhythmogenic ventricular dysplasia, left dominant form
MONDO:0017470	congenital knee dislocation
MONDO:0005489	dyslexia
MONDO:0005486	tooth agenesis
MONDO:0005485	psychotic disorder
MONDO:0005488	adolescent idiopathic scoliosis
MONDO:0005487	schizoaffective disorder
MONDO:0005482	molar-incisor hypomineralization
MONDO:0005481	contact dermatitis due to nickel
MONDO:0005484	colorectal adenoma
MONDO:0005483	chemotherapy-induced alopecia
MONDO:0005480	contact dermatitis
MONDO:0017479	amelia of upper limb, bilateral
MONDO:0017475	macrodactyly of toes
MONDO:0017476	upper limb hypertrophy
MONDO:0017477	lower limb hypertrophy
MONDO:0017478	amelia of upper limb, unilateral
MONDO:0017471	congenital patella dislocation
MONDO:0017472	patella aplasia/hypoplasia, unilateral
MONDO:0017473	patella aplasia/hypoplasia, bilateral
MONDO:0017474	macrodactyly of fingers
MONDO:0005497	bone development disease
MONDO:0005496	bile duct carcinoma
MONDO:0005499	brain glioma
MONDO:0005498	botulism
MONDO:0005493	delayed encephalopathy after acute carbon monoxide poisoning
MONDO:0005492	urticaria
MONDO:0005495	adrenal gland disease
MONDO:0005494	triple-negative breast carcinoma
MONDO:0005491	Chagas cardiomyopathy
MONDO:0005490	large artery stroke
MONDO:0017468	congenital shoulder dislocation
MONDO:0017469	congenital elbow dislocation
MONDO:0017464	congenital pseudoarthrosis of the fibula
MONDO:0017465	congenital pseudoarthrosis of the radius
MONDO:0017466	congenital pseudoarthrosis of the ulna
MONDO:0017467	tibio-fibular synostosis
MONDO:0017460	syndactyly type 6
MONDO:0017461	familial isolated clinodactyly of fingers
MONDO:0017462	congenital pseudoarthrosis of the tibia
MONDO:0017463	congenital pseudoarthrosis of the femur
MONDO:0005468	hypotensive disorder
MONDO:0005467	occupation-related stress disorder
MONDO:0005469	orthostatic hypotension
MONDO:0005464	rhegmatogenous retinal detachment
MONDO:0005463	aortic valve calcification
MONDO:0005466	hypersomnia
MONDO:0005465	methamphetamine-induced psychosis
MONDO:0005460	swine influenza
MONDO:0005462	primitive neuroectodermal tumor
MONDO:0005461	endometrium adenocarcinoma
MONDO:0017457	Preaxial polydactyly of toes
MONDO:0017458	postaxial polydactyly of toes
MONDO:0017459	central polydactyly of toes
MONDO:0017453	fetal parvovirus syndrome
MONDO:0017454	triphalangeal thumb-polysyndactyly syndrome
MONDO:0017455	hyperphalangy
MONDO:0017456	central polydactyly of fingers
MONDO:0017450	split foot
MONDO:0017451	non-syndromic brachydactyly of fingers
MONDO:0017452	non-syndromic brachydactyly of toes
MONDO:0005479	atrial tachycardia
MONDO:0005478	torsades de pointes
MONDO:0005475	migraine with aura
MONDO:0005474	non-small cell lung adenocarcinoma
MONDO:0005477	ventricular tachycardia
MONDO:0005476	atrioventricular node disease
MONDO:0005471	neurally mediated hypotension
MONDO:0005470	postprandial hypotension
MONDO:0005473	temporomandibular joint disorder
MONDO:0005472	congenital heart malformation
MONDO:0017446	apodia
MONDO:0017447	congenital absence/hypoplasia of thumb
MONDO:0017448	congenital absence/hypoplasia of fingers excluding thumb
MONDO:0017449	split hand
MONDO:0017442	congenital absence of thigh and lower leg with foot present
MONDO:0017443	congenital absence of both forearm and hand
MONDO:0017444	congenital absence of both lower leg and foot
MONDO:0017445	acheiria
MONDO:0017440	humeral agenesis/hypoplasia
MONDO:0017441	congenital absence of upper arm and forearm with hand present
MONDO:0005406	gestational diabetes
MONDO:0005405	childhood onset asthma
MONDO:0005408	diabetes mellitus type 2 associated cataract
MONDO:0005407	childhood eosinophilic esophagitis
MONDO:0005402	lymphoid leukemia
MONDO:0005401	colonic neoplasm
MONDO:0005404	myalgic encephalomeyelitis/chronic fatigue syndrome
MONDO:0005403	neonatal systemic lupus erthematosus
MONDO:0005400	ventricular fibrillation
MONDO:0005417	wet macular degeneration
MONDO:0005416	osteoarthritis, knee
MONDO:0005419	metamphetamine dependence
MONDO:0005418	non-compaction cardiomyopathy
MONDO:0005413	cystic fibrosis associated meconium ileus
MONDO:0005412	duodenal ulcer
MONDO:0005415	acute lung injury
MONDO:0005414	treatment-refractory schizophrenia
MONDO:0005411	gallbladder cancer
MONDO:0005410	acute graft vs. host disease
MONDO:0005409	variant Creutzfeld Jacob disease
MONDO:0030293	angioedema, hereditary, 5
MONDO:0030298	angioedema, hereditary, 8
MONDO:0030294	megacystis-microcolon-intestinal hypoperistalsis syndrome 3
MONDO:0030296	megacystis-microcolon-intestinal hypoperistalsis syndrome 4
MONDO:0017270	autosomal ichthyosis syndrome
MONDO:0017271	autosomal ichthyosis syndrome with prominent hair abnormalities
MONDO:0017272	autosomal ichthyosis syndrome with prominent neurologics signs
MONDO:0005288	intestinal polyp
MONDO:0042233	disseminated candidiasis
MONDO:0005287	developmental disability
MONDO:0005289	paranasal sinus neoplasm
MONDO:0005284	chronic progressive multiple sclerosis
MONDO:0005283	retinal disease
MONDO:0005286	palatal neoplasm
MONDO:0005285	kidney stone
MONDO:0005280	prostatitis
MONDO:0005282	cutaneous lupus erythematosus
MONDO:0005281	gallbladder disease
MONDO:0044889	high grade B-cell lymphoma
MONDO:0017277	partial deletion of chromosome 12
MONDO:0017278	autoimmune polyendocrinopathy
MONDO:0017279	young-onset Parkinson disease
MONDO:0017273	autosomal ichthyosis syndrome with fatal disease course
MONDO:0017274	autosomal ichthyosis syndrome with other associated signs
MONDO:0017275	spastic paraplegia-facial-cutaneous lesions syndrome
MONDO:0017276	frontotemporal dementia
MONDO:0017260	systemic diseases with posterior uveitis
MONDO:0017261	systemic diseases with panuveitis
MONDO:0030259	pontocerebellar hypoplasia, type 15
MONDO:0030258	pontocerebellar hypoplasia, type 14
MONDO:0005299	brain ischemia
MONDO:0005298	osteoporosis
MONDO:0005295	intermittent vascular claudication
MONDO:0005294	peripheral vascular disease
MONDO:0005297	urethritis
MONDO:0005296	sleep apnea syndrome
MONDO:0005291	brain aneurysm
MONDO:0005290	rhabdomyolysis
MONDO:0005293	flatfoot
MONDO:0030260	pontocerebellar hypoplasia, type 1E
MONDO:0005292	colitis
MONDO:0030266	immunodeficiency 80 with or without congenital cardiomyopathy
MONDO:0017266	keratinopathic ichthyosis
MONDO:0017267	self-healing collodion baby
MONDO:0030268	developmental and epileptic encephalopathy 6B
MONDO:0017268	acral self-healing collodion baby
MONDO:0017269	X-linked ichthyosis syndrome
MONDO:0017262	inherited non-syndromic ichthyosis
MONDO:0017263	inherited ichthyosis syndromic form
MONDO:0030261	pontocerebellar hypoplasia, type 1F
MONDO:0017264	syndromic recessive X-linked ichthyosis
MONDO:0017265	autosomal recessive congenital ichthyosis
MONDO:0030263	leukodystrophy, hypomyelinating, 21
MONDO:0017250	congenital pulmonary airway malformation type 2
MONDO:0005269	carotid artery disease
MONDO:0005266	diabetic retinopathy
MONDO:0005265	inflammatory bowel disease
MONDO:0005268	Hashimoto's thyroiditis
MONDO:0005267	heart disease
MONDO:0005262	central nervous system cyst
MONDO:0005261	pervasive developmental disorder - not otherwise specified
MONDO:0005264	transient ischemic attack
MONDO:0005263	unipolar depression
MONDO:0005260	autism
MONDO:0030270	lymphatic malformation 9
MONDO:0017259	systemic diseases with anterior uveitis
MONDO:0017255	panuveitis
MONDO:0017256	idiopathic anterior uveitis
MONDO:0017257	idiopathic posterior uveitis
MONDO:0017258	idiopathic panuveitis
MONDO:0017251	congenital pulmonary airway malformation type 3
MONDO:0017252	congenital pulmonary airway malformation type 4
MONDO:0017253	anterior uveitis
MONDO:0017254	posterior uveitis
MONDO:0005277	migraine disorder
MONDO:0005276	dental caries
MONDO:0005279	pulmonary embolism
MONDO:0005278	serous adenocarcinoma
MONDO:0005273	refractory anemia with excess blasts
MONDO:0005272	refractory anemia
MONDO:0005275	lung disease
MONDO:0005271	allergic disease
MONDO:0005270	motor neuron disease
MONDO:0030281	arthrogryposis multiplex congenita 6
MONDO:0017248	congenital pulmonary airway malformation type 0
MONDO:0017249	congenital pulmonary airway malformation type 1
MONDO:0017244	pseudoxanthomatous diffuse cutaneous mastocytosis
MONDO:0017245	intralobar congenital pulmonary sequestration
MONDO:0017246	extralobar congenital pulmonary sequestration
MONDO:0017247	communicating congenital bronchopulmonary-foregut malformation
MONDO:0017240	acrodysostosis with multiple hormone resistance
MONDO:0017241	AP4-related intellectual disability and spastic paraplegia
MONDO:0017242	cutaneous collagenous vasculopathy
MONDO:0017243	bullous diffuse cutaneous mastocytosis
MONDO:0032869	mitochondrial complex 5 (ATP synthase) deficiency, nuclear type 6
MONDO:0032867	pancreatic cancer, susceptibility to, 5
MONDO:0032868	lessel-kubisch syndrome
MONDO:0032865	pulmonary fibrosis and/or bone marrow failure, telomere-related, 5
MONDO:0032866	cortical dysplasia, complex, with other brain malformations 10
MONDO:0032874	ciliary dyskinesia, primary, 43
MONDO:0032875	short stature and microcephaly with genital anomalies
MONDO:0032872	ciliary dyskinesia, primary, 42
MONDO:0032873	retinitis pigmentosa 87 with choroidal involvement
MONDO:0032870	intellectual developmental disorder with short stature and behavioral abnormalities
MONDO:0032871	leukodystrophy, hypomyelinating, 19, transient infantile
MONDO:0032878	neurodevelopmental disorder with behavioral abnormalities, absent speech, and hypotonia
MONDO:0032879	megabladder, congenital
MONDO:0032876	neurodevelopmental disorder with absent language and variable seizures
MONDO:0032877	neurodevelopmental disorder with nonspecific brain abnormalities and with or without seizures
MONDO:0032885	spondyloepimetaphyseal dysplasia, Isidor-Toutain type
MONDO:0032886	Liang-Wang syndrome
MONDO:0032883	intellectual developmental disorder with behavioral abnormalities and craniofacial dysmorphism with or without seizures
MONDO:0032884	ectodermal dysplasia with facial dysmorphism and acral, ocular, and brain anomalies
MONDO:0032881	premature ovarian failure 16
MONDO:0032882	Heyn-Sproul-Jackson syndrome
MONDO:0032880	developmental and epileptic encephalopathy, 82
MONDO:0017291	reversible cerebral vasoconstriction syndrome
MONDO:0017292	well-differentiated fetal adenocarcinoma of the lung
MONDO:0017293	small cell carcinoma of the bladder
MONDO:0017294	glycerol kinase deficiency, infantile form
MONDO:0032889	Poirier-Bienvenu neurodevelopmental syndrome
MONDO:0032887	neurodevelopmental disorder with microcephaly, cortical malformations, and spasticity
MONDO:0032888	neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies
MONDO:0017290	familial intrahepatic cholestasis
MONDO:0044874	refractory cytopenia of childhood
MONDO:0044873	childhood myelodysplastic syndrome
MONDO:0044876	drug hypersensitivity syndrome
MONDO:0044875	coronary microvascular disease
MONDO:0044870	acquired torsion dystonia
MONDO:0044872	dysautonomia
MONDO:0044871	dystonia, focal, task-specific
MONDO:0032896	spermatogenic failure 42
MONDO:0017299	acute annular outer retinopathy
MONDO:0032897	intellectual developmental disorder with hypotonia and behavioral abnormalities
MONDO:0032894	neurodevelopmental disorder with epilepsy, spasticity, and brain atrophy
MONDO:0032895	developmental and epileptic encephalopathy, 83
MONDO:0032892	structural brain anomalies with impaired intellectual development and craniosynostosis
MONDO:0017295	glycerol kinase deficiency, juvenile form
MONDO:0032893	pachygyria, microcephaly, developmental delay, and dysmorphic facies, with or without seizures
MONDO:0017296	glycerol kinase deficiency, adult form
MONDO:0017297	chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids
MONDO:0032890	neuromuscular disease and ocular or auditory anomalies with or without seizures
MONDO:0017298	acute zonal occult outer retinopathy
MONDO:0032891	aneurysm, intracranial berry, 12
MONDO:0017280	demodicidosis
MONDO:0017281	renal caliceal diverticuli-deafness syndrome
MONDO:0017282	alveolar echinococcosis
MONDO:0017283	facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion
MONDO:0032898	spermatogenic failure 43
MONDO:0032899	neutropenia, severe congenital, 8, autosomal dominant
MONDO:0044885	tonsillar lipoma
MONDO:0044884	tonsillar lymphoma
MONDO:0044887	central nervous system non-hodgkin lymphoma
MONDO:0044881	hematopoietic and lymphoid cell neoplasm
MONDO:0044880	cystic tumor of the pancreas
MONDO:0044878	adult germ cell tumor
MONDO:0044877	paraneoplastic cerebellar degeneration
MONDO:0044879	pancreatic mucinous-cystic neoplasm
MONDO:0017288	DICER1 syndrome
MONDO:0017289	fetal lung interstitial tumor
MONDO:0017284	Xp22.13p22.2 duplication syndrome
MONDO:0017285	penoscrotal transposition
MONDO:0017286	tempi syndrome
MONDO:0017287	IgG4-related disease
MONDO:0005329	vascular sarcoma
MONDO:0005328	eye disease
MONDO:0007988	autosomal dominant primary microcephaly
MONDO:0005325	radius fracture
MONDO:0005324	seasonal allergic rhinitis
MONDO:0007989	congenital microcoria
MONDO:0007986	metatropic dysplasia
MONDO:0005327	hip fracture
MONDO:0032942	neurodevelopmental disorder with microcephaly and dysmorphic facies
MONDO:0007987	Kniest dysplasia
MONDO:0032943	neurodevelopmental disorder with relative macrocephaly and with or without cardiac or endocrine anomalies
MONDO:0005326	sunburn
MONDO:0005321	Fuchs' endothelial dystrophy
MONDO:0007984	metaphyseal dysplasia-maxillary hypoplasia-brachydacty syndrome
MONDO:0007985	metatarsus varus, type 1
MONDO:0005320	tibia fracture
MONDO:0007982	metaphyseal chondrodysplasia, Jansen type
MONDO:0005323	bacterial sexually transmitted disease
MONDO:0005322	ulna fracture
MONDO:0007983	Schmid metaphyseal chondrodysplasia
MONDO:0007980	metachromasia of fibroblasts
MONDO:0007981	metachromatic leukodystrophy, adult-onset, with normal arylsulfatase A
MONDO:0020959	Mansonella ozzardi infection
MONDO:0044926	oropharyngeal carcinoma
MONDO:0017318	phakomatosis pigmentovascularis
MONDO:0044925	oral cavity carcinoma
MONDO:0017319	hereditary elliptocytosis
MONDO:0017314	Ehlers-Danlos syndrome, vascular type
MONDO:0019977	parkinsonism with dementia of Guadeloupe
MONDO:0017315	short stature-webbed neck-heart disease syndrome
MONDO:0044921	atypical lymphoproliferative disorder
MONDO:0019976	dementia pugilistica
MONDO:0017316	short stature-deafness-neutrophil dysfunction-dysmorphism syndrome
MONDO:0019979	renal hypoplasia, unilateral
MONDO:0044924	acute myeloid leukemia with mutated CEBPA
MONDO:0019978	Robinow syndrome
MONDO:0017317	phakomatosis pigmentokeratotica
MONDO:0044923	acute myeloid leukemia with mutated NPM1
MONDO:0019973	persistent placoid maculopathy
MONDO:0017310	Marfan and Marfan-related disorder
MONDO:0017311	rare disease with thoracic aortic aneurysm and aortic dissection
MONDO:0019972	dural sinus malformation
MONDO:0017312	Perrault syndrome
MONDO:0019975	pellagra
MONDO:0017313	disorder of folate metabolism and transport
MONDO:0019974	postencephalitic parkinsonism
MONDO:0019971	melanoma of soft tissue
MONDO:0019970	Sinding-Larsen-Johansson disease
MONDO:0005339	androgenetic alopecia
MONDO:0005336	myopathy
MONDO:0007999	holoprosencephaly 2
MONDO:0005335	colorectal neoplasm
MONDO:0005338	open-angle glaucoma
MONDO:0007997	microspherophakia with hernia
MONDO:0007998	microspherophakia-metaphyseal dysplasia syndrome
MONDO:0005337	neuropathy
MONDO:0007995	microphthalmia, isolated, with cataract 1
MONDO:0020950	viral eye infection
MONDO:0005331	acrocephalosyndactylia
MONDO:0007996	microphthalmia, isolated, with corectopia
MONDO:0005334	hereditary nephritis
MONDO:0007993	microgastria-limb reduction defect syndrome
MONDO:0005333	hyperthyroxinemia
MONDO:0007994	micromelic bone dysplasia with cloverleaf skull
MONDO:0007991	microcephaly-deafness-intellectual disability syndrome
MONDO:0007992	microcornea-glaucoma-absent frontal sinuses syndrome
MONDO:0005330	angiosarcoma
MONDO:0007990	multiple benign circumferential skin creases on limbs
MONDO:0044937	rectal carcinoma
MONDO:0017307	disorder of tyrosine metabolism
MONDO:0017308	Marfan syndrome type 2
MONDO:0020947	parasitic eye infection
MONDO:0019969	panner disease
MONDO:0017309	neonatal Marfan syndrome
MONDO:0020944	fungal infection of eye
MONDO:0017303	qualitative or quantitative defects of tropomyosin
MONDO:0019966	thoracic outlet syndrome
MONDO:0019965	rare benign ovarian tumor
MONDO:0017304	ocular albinism
MONDO:0017305	syndromic oculocutaneous albinism
MONDO:0019968	Osgood-Schlatter disease
MONDO:0019967	Kienbock disease
MONDO:0017306	disorder of phenylalanine metabolism
MONDO:0019962	thyroid lymphoma
MONDO:0017300	congenital pericardium anomaly
MONDO:0019961	somatostatinoma
MONDO:0017301	pericardial and diaphragmatic defect
MONDO:0019964	thymic neuroendocrine tumor
MONDO:0017302	qualitative or quantitative defects of troponin
MONDO:0019963	bronchial endocrine tumor
MONDO:0030300	cardiomyopathy, dilated, 2D
MONDO:0019960	VIPoma
MONDO:0030307	spermatogenic failure 55
MONDO:0005307	contracture
MONDO:0005306	ankylosing spondylitis
MONDO:0030309	Leber hereditary optic neuropathy, autosomal recessive
MONDO:0005309	spinal fracture
MONDO:0007968	melanoma tumor antigen Gp90
MONDO:0007969	Melkersson-Rosenthal syndrome
MONDO:0005308	ciliopathy
MONDO:0030308	immunodeficiency 82 with systemic inflammation
MONDO:0005303	drug dependence
MONDO:0007966	susceptibility to uveal melanoma
MONDO:0007967	melanoma and neural system tumor syndrome
MONDO:0005302	attention deficit hyperactivity disorder, inattentive type
MONDO:0030302	immunodeficiency 81
MONDO:0007964	melanoma, cutaneous malignant, susceptibility to, 2
MONDO:0005305	epistaxis
MONDO:0005304	biliary tract neoplasm
MONDO:0007965	melanoma, malignant familial intraocular
MONDO:0007962	Megalodactyly
MONDO:0007963	melanoma, cutaneous malignant, susceptibility to, 1
MONDO:0005301	multiple sclerosis
MONDO:0007960	megacystis-microcolon-intestinal hypoperistalsis syndrome
MONDO:0005300	chronic kidney disease
MONDO:0007961	megalencephaly, autosomal dominant
MONDO:0019959	glucagonoma
MONDO:0020937	contractures, pterygia, and variable skeletal fusions syndrome
MONDO:0019958	insulinoma
MONDO:0019955	GRFoma
MONDO:0019954	pancreatic neuroendocrine tumor
MONDO:0019957	PPoma
MONDO:0019956	encephalitis
MONDO:0019951	rigid spine syndrome
MONDO:0019950	congenital muscular dystrophy
MONDO:0030312	spinocerebellar ataxia, autosomal recessive 29
MONDO:0019953	mega-cisterna magna
MONDO:0019952	congenital myopathy
MONDO:0030311	combined oxidative phosphorylation deficiency 52
MONDO:0005318	canker sore
MONDO:0030318	spinocerebellar ataxia, autosomal recessive 30
MONDO:0030317	cardiomyopathy, familial hypertrophic, 28
MONDO:0005317	fatty liver
MONDO:0007979	metachondromatosis
MONDO:0005319	humerus fracture
MONDO:0007977	mesomelic dysplasia, Kantaputra type
MONDO:0005314	relapsing-remitting multiple sclerosis
MONDO:0030314	inflammatory bowel disease (infantile ulcerative colitis) 31, autosomal recessive
MONDO:0005313	necrotizing enterocolitis
MONDO:0030313	encephalopathy, acute, infection-induced (herpes-specific), susceptibility to, 10
MONDO:0007978	malignant mesothelioma
MONDO:0005316	bacterial vaginosis
MONDO:0007975	meralgia paraesthetica, familial
MONDO:0030316	lymphatic malformation 11
MONDO:0005315	bone fracture
MONDO:0007976	mesomelic dwarfism of hypoplastic tibia and radius type
MONDO:0005310	atrial flutter
MONDO:0007973	mental and growth retardation with amblyopia
MONDO:0007974	intellectual disability, autosomal dominant 1
MONDO:0005312	pouchitis
MONDO:0007971	delayed membranous cranial ossification
MONDO:0044964	oral cavity mucoepidermoid carcinoma
MONDO:0005311	atherosclerosis
MONDO:0007972	Meniere disease
MONDO:0007970	melorheostosis
MONDO:0019948	reducing body myopathy
MONDO:0019947	rippling muscle disease 2
MONDO:0019949	zebra body myopathy
MONDO:0019944	Eisenmenger syndrome
MONDO:0019943	hereditary continuous muscle fiber activity
MONDO:0020920	escherichia coli infection
MONDO:0019946	ligneous conjunctivitis
MONDO:0019945	solar urticaria
MONDO:0044956	paranasal sinus mucoepidermoid carcinoma
MONDO:0019940	hypertrichosis-acromegaloid facial appearance syndrome
MONDO:0019942	distal arthrogryposis
MONDO:0030323	spinocerebellar ataxia, autosomal recessive 31
MONDO:0019941	hereditary sensory and autonomic neuropathy type 2
MONDO:0020927	postaxial polydactyly
MONDO:0032904	corneal dystrophy, Meesmann, 2
MONDO:0032905	spastic paraplegia 81, autosomal recessive
MONDO:0032902	Joubert syndrome 36
MONDO:0032903	arthrogryposis multiplex congenita 4, neurogenic, with agenesis of the corpus callosum
MONDO:0032900	neurodevelopmental disorder with hypotonia and autistic features with or without hyperkinetic movements
MONDO:0005369	carcinoid tumor
MONDO:0032901	Catifa syndrome
MONDO:0005368	obsessive-compulsive disorder
MONDO:0005365	hearing loss disorder
MONDO:0005364	Graves disease
MONDO:0005367	heroin dependence
MONDO:0005366	chronic hepatitis B virus infection
MONDO:0005361	eosinophilic esophagitis
MONDO:0032908	CEBALID syndrome
MONDO:0005360	Dupuytren contracture
MONDO:0032909	mitochondrial complex 3 deficiency, nuclear type 10
MONDO:0005363	focal segmental glomerulosclerosis
MONDO:0032906	spastic paraplegia 82, autosomal recessive
MONDO:0005362	erectile dysfunction
MONDO:0032907	lymphatic malformation 8
MONDO:0020999	genetic chronic primary adrenal insufficiency
MONDO:0017358	organic aciduria
MONDO:0017359	3-methylglutaconic aciduria
MONDO:0017354	infantile glycine encephalopathy
MONDO:0017355	inborn disorder of proline metabolism
MONDO:0017356	inborn disorder of ornithine metabolism
MONDO:0017357	transient hyperammonemia of the newborn
MONDO:0017350	inborn disorder of tryptophan metabolism
MONDO:0017351	inborn disorder of lysine and hydroxylysine metabolism
MONDO:0017352	disorder of glutamine metabolism
MONDO:0017353	neonatal glycine encephalopathy
MONDO:0032915	long QT syndrome 16
MONDO:0032916	Imagawa-Matsumoto syndrome
MONDO:0032913	congenital heart defects, multiple types, 7
MONDO:0032914	ciliary dyskinesia, primary, 44
MONDO:0032911	deafness, autosomal dominant 75
MONDO:0005379	neurotic disorder
MONDO:0032912	Coffin-Siris syndrome 11
MONDO:0032910	mitochondrial complex 1 deficiency, nuclear type 34
MONDO:0005376	membranous glomerulonephritis
MONDO:0005375	nasopharyngeal neoplasm
MONDO:0005378	neuromyelitis optica
MONDO:0005377	nephrotic syndrome
MONDO:0032919	intellectual developmental disorder 62
MONDO:0005372	male infertility
MONDO:0005371	mood disorder
MONDO:0005374	bone marrow neoplasm
MONDO:0032917	deafness, autosomal dominant 76
MONDO:0032918	developmental and epileptic encephalopathy, 84
MONDO:0005373	meningococcal infection
MONDO:0005370	interstitial lung disease
MONDO:0020989	hereditary persistence of fetal hemoglobin
MONDO:0017347	plasmablastic lymphoma
MONDO:0017348	lymphoepithelial-like carcinoma
MONDO:0017349	myopericytoma
MONDO:0017343	Epstein-Barr virus-associated malignant lymphoproliferative disorder
MONDO:0017344	Epstein-Barr virus-associated carcinoma
MONDO:0017345	Epstein-Barr virus-associated mesenchymal tumor
MONDO:0017346	Epstein-Barr virus-positive diffuse large B-cell lymphoma of the elderly
MONDO:0017340	juvenile nasopharyngeal angiofibroma
MONDO:0017341	virus associated tumor
MONDO:0017342	Epstein-Barr virus-related tumor
MONDO:0032926	sandestig-stefanova syndrome
MONDO:0032927	triokinase and FMN cyclase deficiency syndrome
MONDO:0032924	ciliary dyskinesia, primary, 45
MONDO:0032925	respiratory papillomatosis, juvenile recurrent, congenital
MONDO:0005347	hypertriglyceridemia
MONDO:0032922	Beck-Fahrner syndrome
MONDO:0032923	spinocerebellar ataxia, autosomal recessive 28
MONDO:0005346	gallstones
MONDO:0005349	otosclerosis
MONDO:0032920	juvenile arthritis due to defect in LACC1
MONDO:0005348	keloid
MONDO:0032921	neurodevelopmental disorder with hypotonia, neonatal respiratory insufficiency, and thermodysregulation
MONDO:0005343	viral human hepatitis
MONDO:0020983	myocardial rupture
MONDO:0005342	IgA glomerulonephritis
MONDO:0005345	hypospadias
MONDO:0005344	hepatitis B virus infection
MONDO:0020980	hair nevus
MONDO:0005341	skin basal cell carcinoma
MONDO:0032928	T-cell lymphopenia, infantile, with or without nail dystrophy, autosomal dominant
MONDO:0005340	alopecia areata
MONDO:0044903	myelofibrosis
MONDO:0044906	bladder urothelial papilloma
MONDO:0020979	pilosebaceous hamartoma
MONDO:0020977	granulomatous prostatitis
MONDO:0019999	intestinal malformation
MONDO:0017336	fatal infantile hypertrophic cardiomyopathy due to mitochondrial complex I deficiency
MONDO:0019998	gastroduodenal malformation
MONDO:0017337	inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency
MONDO:0017338	fatal multiple mitochondrial dysfunctions syndrome
MONDO:0020974	laryngeal granuloma
MONDO:0017339	exfoliative ichthyosis
MONDO:0019995	peripheral resistance to thyroid hormones
MONDO:0017332	pyoderma gangrenosum-acne-suppurative hidradenitis syndrome
MONDO:0032930	intellectual developmental disorder with poor growth and with or without seizures or ataxia
MONDO:0019994	maternal uniparental disomy of chromosome 13
MONDO:0017333	hypomyelinating leukodystrophy with or without oligondontia and/or hypogonadism
MONDO:0017334	12q15q21.1 microdeletion syndrome
MONDO:0019997	rare gastroenterologic disease
MONDO:0017335	microtriplication 11q24.1
MONDO:0019996	rare cardiac disease
MONDO:0019991	immunotactoid glomerulopathy
MONDO:0019990	non-amyloid fibrillary glomerulopathy
MONDO:0044907	metastatic squamous cell carcinoma
MONDO:0017330	malignancy diagnosed during pregnancy
MONDO:0019993	congenital renal artery stenosis
MONDO:0017331	Pilotto syndrome
MONDO:0019992	pseudohypoparathyroidism
MONDO:0032937	myopathy, congenital proximal, with minicore lesions
MONDO:0032938	basal ganglia calcification, idiopathic, 8, autosomal recessive
MONDO:0032935	rhizomelic limb shortening with dysmorphic features
MONDO:0032936	myopathy, congenital, with respiratory insufficiency and bone fractures
MONDO:0005358	Dengue hemorrhagic fever
MONDO:0032933	chromosome 1p36.33 duplication syndrome, atad3 gene cluster, autosomal dominant
MONDO:0005357	Creutzfeldt Jacob disease
MONDO:0032934	genitourinary and/or brain malformation syndrome
MONDO:0032931	pontocerebellar hypoplasia, hypotonia, and respiratory insufficiency syndrome, neonatal lethal
MONDO:0005359	drug-induced liver injury
MONDO:0032932	mitochondrial DNA depletion syndrome 18
MONDO:0005354	chronic hepatitis C virus infection
MONDO:0005353	marijuana dependence
MONDO:0005356	coronary vasospasm
MONDO:0020971	gonococcal urethritis
MONDO:0005355	coronary restenosis
MONDO:0005350	abdominal aortic aneurysm
MONDO:0032939	intellectual developmental disorder, autosomal dominant 63, with macrocephaly
MONDO:0005352	conduct disorder
MONDO:0005351	anorexia nervosa
MONDO:0044915	salivary duct carcinoma
MONDO:0017329	familial vesicoureteral reflux
MONDO:0044917	T-lymphoblastic lymphoma
MONDO:0044916	extrarenal rhabdoid tumor
MONDO:0019988	pauci-immune glomerulonephritis with ANCA
MONDO:0017325	early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation
MONDO:0019987	congenital and infantile nephrotic syndrome
MONDO:0017326	infective dermatitis associated with HTLV-1
MONDO:0017327	primary non-gestational choriocarcinoma of ovary
MONDO:0044913	metastatic malignant neoplasm in the eye
MONDO:0019989	pauci-immune glomerulonephritis without ANCA
MONDO:0044912	metastatic malignant neoplasm in the spinal cord
MONDO:0017328	non-central nervous system-localized embryonal carcinoma
MONDO:0032940	retinitis pigmentosa 88
MONDO:0019984	renal tubular dysgenesis due to twin-twin transfusion
MONDO:0017321	pili torti-onychodysplasia syndrome
MONDO:0019983	multiloculated renal cyst
MONDO:0017322	disorders of vitamin D metabolism
MONDO:0032941	myopia 27
MONDO:0019986	sporadic idiopathic steroid-resistant nephrotic syndrome with collapsing glomerulopathy
MONDO:0017323	hypocalcemic rickets
MONDO:0019985	drug-related renal tubular dysgenesis
MONDO:0017324	autosomal recessive hypophosphatemic rickets
MONDO:0044919	malignant renal pelvis neoplasm
MONDO:0019980	renal hypoplasia, bilateral
MONDO:0019982	bilateral multicystic dysplastic kidney
MONDO:0019981	unilateral multicystic dysplastic kidney
MONDO:0017320	phosphoenolpyruvate carboxykinase deficiency
MONDO:0007904	median nodule of the upper lip
MONDO:0007905	lip, hamartomatous
MONDO:0007902	lichen planus, familial
MONDO:0007903	Li-Fraumeni syndrome 1
MONDO:0007900	nonsyndromic congenital nail disorder 3
MONDO:0007901	levator-medial rectus synkinesis
MONDO:0007915	systemic lupus erythematosus
MONDO:0007916	primary intestinal lymphangiectasia
MONDO:0007913	low density lipoprotein, variation in molecular weight of
MONDO:0007914	lumbar stenosis, familial
MONDO:0007911	lipoprotein, variant of beta
MONDO:0007912	lithium transport
MONDO:0007910	lipoprotein types--Lt system
MONDO:0007908	multiple symmetric lipomatosis
MONDO:0007909	familial multiple lipomatosis
MONDO:0007906	familial partial lipodystrophy, Dunnigan type
MONDO:0007907	lipoma of the conjunctiva
MONDO:0007948	marfanoid hypermobility syndrome
MONDO:0007949	Marshall syndrome
MONDO:0007946	jaw-winking syndrome
MONDO:0007947	Marfan syndrome
MONDO:0007944	Treacher-Collins syndrome 1
MONDO:0007945	mannose 6-phosphate receptor recognition defect, Lebanese type
MONDO:0007942	Mammastatin
MONDO:0007943	Nager acrofacial dysostosis
MONDO:0007940	malignant hyperthermia, susceptibility to, 3
MONDO:0007941	malocclusion due to protuberant upper front teeth
MONDO:0019929	49,XXXXY syndrome
MONDO:0019937	rare gynecologic or obstetric disease
MONDO:0019936	rare otorhinolaryngological malformation
MONDO:0019939	early-onset schizophrenia
MONDO:0019938	anorectal malformation
MONDO:0019933	acromegaly
MONDO:0019932	isolated partial vaginal agenesis
MONDO:0019935	isochromosome Y
MONDO:0019934	polyploidy
MONDO:0019931	Leydig cell hypoplasia due to partial LH resistance
MONDO:0019930	Leydig cell hypoplasia due to complete LH resistance
MONDO:0007939	malignant hyperthermia, susceptibility to, 2
MONDO:0007959	medulloblastoma
MONDO:0007957	mediosternal depigmentation line
MONDO:0007958	familial medullary thyroid carcinoma
MONDO:0007955	Meckel diverticulum
MONDO:0007956	Pai syndrome
MONDO:0007953	Binder syndrome
MONDO:0007954	May-Hegglin anomaly
MONDO:0007951	masticatory muscles, hypertrophy of
MONDO:0007952	maxillofacial dysostosis
MONDO:0007950	mastocytosis
MONDO:0019919	maternal uniparental disomy of chromosome 22
MONDO:0019918	maternal uniparental disomy of chromosome 21
MONDO:0019926	X small rings
MONDO:0019925	paternal uniparental disomy of chromosome 21
MONDO:0019928	48,XXXY syndrome
MONDO:0019927	growth hormone-producing pituitary gland neoplasm
MONDO:0019922	paternal uniparental disomy of chromosome 7
MONDO:0019921	paternal uniparental disomy of chromosome 6
MONDO:0019924	paternal uniparental disomy of chromosome 20
MONDO:0019923	Beckwith-Wiedemann syndrome due to paternal uniparental disomy of chromosome 11
MONDO:0019920	paternal uniparental disomy of chromosome 5
MONDO:0007926	Waldenstrom macroglobulinemia
MONDO:0007927	congenital macroglossia
MONDO:0007924	Bannayan-Riley-Ruvalcaba syndrome
MONDO:0007925	chromosome 5q deletion syndrome
MONDO:0007922	lymphedema-distichiasis syndrome
MONDO:0007923	macrocephaly, benign familial
MONDO:0007920	lymphatic malformation 5
MONDO:0007921	yellow nail syndrome
MONDO:0019908	ring chromosome 15
MONDO:0019907	ring chromosome 13
MONDO:0019909	ring chromosome 16
MONDO:0019915	maternal uniparental disomy of chromosome 14
MONDO:0019914	maternal uniparental disomy of chromosome 9
MONDO:0019917	maternal uniparental disomy of chromosome 20
MONDO:0019916	maternal uniparental disomy of chromosome 16
MONDO:0019911	maternal uniparental disomy of chromosome 4
MONDO:0019910	maternal uniparental disomy of chromosome 2
MONDO:0019913	silver-Russell syndrome due to maternal uniparental disomy of chromosome 7
MONDO:0019912	maternal uniparental disomy of chromosome 6
MONDO:0007919	lymphatic malformation 1
MONDO:0007917	lymphedema-cerebral arteriovenous anomaly syndrome
MONDO:0007918	microcephaly with or without chorioretinopathy, lymphedema, or intellectual disability
MONDO:0007937	renal hypomagnesemia 2
MONDO:0007938	46,XY sex reversal 4
MONDO:0007935	cystoid macular edema
MONDO:0007936	macular dystrophy, fenestrated sheen type
MONDO:0007933	vitelliform macular dystrophy 1
MONDO:0007934	benign concentric annular macular dystrophy
MONDO:0007931	vitelliform macular dystrophy 2
MONDO:0007932	age related macular degeneration 2
MONDO:0007930	Bernard-Soulier syndrome, type A2, autosomal dominant
MONDO:0019904	ring chromosome 3
MONDO:0019903	ring chromosome 2
MONDO:0019906	ring chromosome 11
MONDO:0019905	ring chromosome 9
MONDO:0019900	non-distal monosomy 12q
MONDO:0019902	monosomy 13q34
MONDO:0019901	non-distal monosomy 20q
MONDO:0007928	Fechtner syndrome
MONDO:0007929	Epstein syndrome
MONDO:0024193	portal hypertension, noncirrhotic
MONDO:0024189	neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset
MONDO:8000008	Martsolf syndrome 1
MONDO:8000006	WHIM syndrome 1
MONDO:8000010	antiphospholipid syndrome
MONDO:8000019	vertigo, benign recurrent, 1
MONDO:8000015	46,XY sex reversal 11
MONDO:8000018	benign paroxysmal positional vertigo
MONDO:8000017	testicular regression syndrome
MONDO:8000012	neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset 1
MONDO:8000011	visceral neuropathy, familial, 1, autosomal recessive
MONDO:8000014	familial antiphospholipid syndrome
MONDO:8000013	portal hypertension, noncirrhotic, 1
MONDO:0700107	chromosome 19q13.11 deletion syndrome, distal
MONDO:0023961	visceral neuropathy, familial
MONDO:0100441	dominant GUCY2D retinopathy
MONDO:0100442	RP2 retinopathy
MONDO:0100443	RDH5 retinopathy
MONDO:0100444	RLBP1 retinopathy
MONDO:0100445	LCA5 retinopathy
MONDO:0100446	CNGB3 retinopathy
MONDO:0100447	ATF6 retinopathy
MONDO:0100448	RAB28 retinopathy
MONDO:0100438	AIPL1 retinopathy
MONDO:0100439	glycogen storage disease IXa2
MONDO:0100450	CAPN5 vitreoretinopathy
MONDO:0100451	CEP290 ciliopathy
MONDO:0100452	dominant RPE65 retinopathy
MONDO:0100453	recessive GUCY2D retinopathy
MONDO:0100454	GUCY2D retinopathy
MONDO:0100455	neonatal-onset developmental and epileptic encephalopathy
MONDO:0100456	neonatal encephalopathy with non-epileptic myoclonus
MONDO:0100449	FLVCR1 retinopathy with or without ataxia
MONDO:0100426	iatrogenic
MONDO:0100430	fibrotic liver disease
MONDO:0100431	migraine without aura
MONDO:0100432	FNIP1-associated syndrome
MONDO:0100433	ACTB-associated syndromic thrombocytopenia
MONDO:0100435	Schwartz-Jampel syndrome type 1
MONDO:0100436	cataract 2, multiple types
MONDO:0100437	RPGR retinopathy
MONDO:0100427	non-iatrogenic
MONDO:0100428	progressive bulbar palsy of childhood
MONDO:0100368	recessive RPE65 retinopathy
MONDO:0100369	iatrogenic or non-iatrogenic
MONDO:0023880	WHIM syndrome
MONDO:0023910	Martsolf syndrome