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Disease: Disease

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Root: KW Hierarchy (Keywords from UniProtKB)

Shortest distance to current term (+ for parents, - for children) KW term [KW ID] <#Children> (#SF|#FA) #Supra-domain
(Single|Duplex|Triple)
0:   Disease [KW:9995] <127>
- 1:   Ciliopathy [KW:1186] <5>(0|0) (0|0|0)
- 1:   Neurodegeneration [KW:0523] <4>(0|0) (0|0|0)
- 1:   Primary mitochondrial disease [KW:1274] <4>(0|0) (0|0|0)
- 1:   Deafness [KW:0209] <3>(0|0) (0|0|0)
- 1:   Hereditary hemolytic anemia [KW:0360] <3>(0|0) (0|0|0)
- 1:   Autism spectrum disorder [KW:1268] <2>(0|0) (0|0|0)
- 1:   Neuropathy [KW:0622] <2>(0|0) (0|0|0)
- 1:   Albinism [KW:0015] <1>(0|0) (0|0|0)
- 1:   Ectodermal dysplasia [KW:0038] <1>(0|0) (0|0|0)
- 1:   Leukodystrophy [KW:1026] <1>(0|0) (0|0|0)
- 1:   Myofibrillar myopathy [KW:1060] <1>(0|0) (0|0|0)
- 1:   Peroxisome biogenesis disorder [KW:0958] <1>(0|0) (0|0|0)
- 1:   AIDS [KW:0014](0|0) (0|0|0)
- 1:   Age-related macular degeneration [KW:0913](0|0) (0|0|0)
- 1:   Aicardi-Goutieres syndrome [KW:0948](0|0) (0|0|0)
- 1:   Allergen [KW:0020](0|0) (0|0|0)
- 1:   Alport syndrome [KW:0023](0|0) (0|0|0)
- 1:   Alzheimer disease [KW:0026](0|0) (0|0|0)
- 1:   Amelogenesis imperfecta [KW:0986](0|0) (0|0|0)
- 1:   Amyloidosis [KW:1008](0|0) (0|0|0)
- 1:   Aortic aneurysm [KW:0993](0|0) (0|0|0)
- 1:   Asthma [KW:1058](0|0) (0|0|0)
- 1:   Atherosclerosis [KW:0065](0|0) (0|0|0)
- 1:   Atrial fibrillation [KW:1020](0|0) (0|0|0)
- 1:   Atrial septal defect [KW:0976](0|0) (0|0|0)
- 1:   Autoimmune encephalomyelitis [KW:0069](0|0) (0|0|0)
- 1:   Autoimmune uveitis [KW:0070](0|0) (0|0|0)
- 1:   Bartter syndrome [KW:0910](0|0) (0|0|0)
- 1:   Bernard Soulier syndrome [KW:0087](0|0) (0|0|0)
- 1:   Brugada syndrome [KW:0992](0|0) (0|0|0)
- 1:   Cardiomyopathy [KW:0122](0|0) (0|0|0)
- 1:   Cataract [KW:0898](0|0) (0|0|0)
- 1:   Chronic granulomatous disease [KW:0161](0|0) (0|0|0)
- 1:   Cockayne syndrome [KW:0172](0|0) (0|0|0)
- 1:   Cone-rod dystrophy [KW:0182](0|0) (0|0|0)
- 1:   Congenital adrenal hyperplasia [KW:0954](0|0) (0|0|0)
- 1:   Congenital disorder of glycosylation [KW:0900](0|0) (0|0|0)
- 1:   Congenital erythrocytosis [KW:0985](0|0) (0|0|0)
- 1:   Congenital generalized lipodystrophy [KW:1022](0|0) (0|0|0)
- 1:   Congenital hypothyroidism [KW:0984](0|0) (0|0|0)
- 1:   Congenital muscular dystrophy [KW:0912](0|0) (0|0|0)
- 1:   Congenital myasthenic syndrome [KW:1004](0|0) (0|0|0)
- 1:   Congenital stationary night blindness [KW:1014](0|0) (0|0|0)
- 1:   Corneal dystrophy [KW:1212](0|0) (0|0|0)
- 1:   Craniosynostosis [KW:0989](0|0) (0|0|0)
- 1:   Crown gall tumor [KW:0192](0|0) (0|0|0)
- 1:   Cushing syndrome [KW:1062](0|0) (0|0|0)
- 1:   Cystinuria [KW:0199](0|0) (0|0|0)
- 1:   Dental caries [KW:0214](0|0) (0|0|0)
- 1:   Diabetes insipidus [KW:0218](0|0) (0|0|0)
- 1:   Diabetes mellitus [KW:0219](0|0) (0|0|0)
- 1:   Diamond-Blackfan anemia [KW:1024](0|0) (0|0|0)
- 1:   Disease mutation [KW:0225](0|0) (0|0|0)
- 1:   Down syndrome [KW:0241](0|0) (0|0|0)
- 1:   Dwarfism [KW:0242](0|0) (0|0|0)
- 1:   Dyskeratosis congenita [KW:1011](0|0) (0|0|0)
- 1:   Dystonia [KW:1023](0|0) (0|0|0)
- 1:   Dystroglycanopathy [KW:1215](0|0) (0|0|0)
- 1:   Ehlers-Danlos syndrome [KW:0248](0|0) (0|0|0)
- 1:   Emery-Dreifuss muscular dystrophy [KW:1067](0|0) (0|0|0)
- 1:   Epidermolysis bullosa [KW:0263](0|0) (0|0|0)
- 1:   Epilepsy [KW:0887](0|0) (0|0|0)
- 1:   Familial hemophagocytic lymphohistiocytosis [KW:0951](0|0) (0|0|0)
- 1:   Fanconi anemia [KW:0923](0|0) (0|0|0)
- 1:   Gangliosidosis [KW:0331](0|0) (0|0|0)
- 1:   Gaucher disease [KW:0307](0|0) (0|0|0)
- 1:   Glaucoma [KW:0955](0|0) (0|0|0)
- 1:   Glutaricaciduria [KW:0316](0|0) (0|0|0)
- 1:   Glycogen storage disease [KW:0322](0|0) (0|0|0)
- 1:   Gout [KW:0335](0|0) (0|0|0)
- 1:   Hemolytic uremic syndrome [KW:1068](0|0) (0|0|0)
- 1:   Hemophilia [KW:0355](0|0) (0|0|0)
- 1:   Hereditary multiple exostoses [KW:0361](0|0) (0|0|0)
- 1:   Hereditary nonpolyposis colorectal cancer [KW:0362](0|0) (0|0|0)
- 1:   Heterotaxy [KW:1056](0|0) (0|0|0)
- 1:   Hirschsprung disease [KW:0367](0|0) (0|0|0)
- 1:   Holoprosencephaly [KW:0370](0|0) (0|0|0)
- 1:   Hyperlipidemia [KW:0380](0|0) (0|0|0)
- 1:   Hypogonadotropic hypogonadism [KW:1016](0|0) (0|0|0)
- 1:   Hypotrichosis [KW:1063](0|0) (0|0|0)
- 1:   Ichthyosis [KW:0977](0|0) (0|0|0)
- 1:   Intrahepatic cholestasis [KW:0988](0|0) (0|0|0)
- 1:   Kallmann syndrome [KW:0956](0|0) (0|0|0)
- 1:   Leber congenital amaurosis [KW:0901](0|0) (0|0|0)
- 1:   Li-Fraumeni syndrome [KW:0435](0|0) (0|0|0)
- 1:   Limb-girdle muscular dystrophy [KW:0947](0|0) (0|0|0)
- 1:   Lissencephaly [KW:0451](0|0) (0|0|0)
- 1:   Long QT syndrome [KW:0454](0|0) (0|0|0)
- 1:   Malaria [KW:0461](0|0) (0|0|0)
- 1:   Maple syrup urine disease [KW:0466](0|0) (0|0|0)
- 1:   Mental retardation [KW:0991](0|0) (0|0|0)
- 1:   Microphthalmia [KW:1013](0|0) (0|0|0)
- 1:   Mucolipidosis [KW:0942](0|0) (0|0|0)
- 1:   Mucopolysaccharidosis [KW:0510](0|0) (0|0|0)
- 1:   Nemaline myopathy [KW:1057](0|0) (0|0|0)
- 1:   Nephronophthisis [KW:0983](0|0) (0|0|0)
- 1:   Niemann-Pick disease [KW:1054](0|0) (0|0|0)
- 1:   Obesity [KW:0550](0|0) (0|0|0)
- 1:   Oncogene [KW:0553](0|0) (0|0|0)
- 1:   Osteogenesis imperfecta [KW:1065](0|0) (0|0|0)
- 1:   Osteopetrosis [KW:0987](0|0) (0|0|0)
- 1:   Palmoplantar keratoderma [KW:1007](0|0) (0|0|0)
- 1:   Parkinson disease [KW:0907](0|0) (0|0|0)
- 1:   Parkinsonism [KW:0908](0|0) (0|0|0)
- 1:   Peters anomaly [KW:1059](0|0) (0|0|0)
- 1:   Phenylketonuria [KW:0586](0|0) (0|0|0)
- 1:   Pontocerebellar hypoplasia [KW:1021](0|0) (0|0|0)
- 1:   Premature ovarian failure [KW:1066](0|0) (0|0|0)
- 1:   Primary hypomagnesemia [KW:0982](0|0) (0|0|0)
- 1:   Primary microcephaly [KW:0905](0|0) (0|0|0)
- 1:   Proto-oncogene [KW:0656](0|0) (0|0|0)
- 1:   Pseudohermaphroditism [KW:0657](0|0) (0|0|0)
- 1:   Retinitis pigmentosa [KW:0682](0|0) (0|0|0)
- 1:   Rhizomelic chondrodysplasia punctata [KW:0685](0|0) (0|0|0)
- 1:   SCID [KW:0705](0|0) (0|0|0)
- 1:   Schizophrenia [KW:1211](0|0) (0|0|0)
- 1:   Short QT syndrome [KW:0940](0|0) (0|0|0)
- 1:   Stargardt disease [KW:0751](0|0) (0|0|0)
- 1:   Stickler syndrome [KW:0757](0|0) (0|0|0)
- 1:   Systemic lupus erythematosus [KW:0772](0|0) (0|0|0)
- 1:   Thrombophilia [KW:0792](0|0) (0|0|0)
- 1:   Trypanosomiasis [KW:0821](0|0) (0|0|0)
- 1:   Tumor suppressor [KW:0043](0|0) (0|0|0)
- 1:   Whooping cough [KW:0855](0|0) (0|0|0)
- 1:   Williams-Beuren syndrome [KW:0856](0|0) (0|0|0)
- 1:   Xeroderma pigmentosum [KW:0857](0|0) (0|0|0)
- 1:   von Willebrand disease [KW:0852](0|0) (0|0|0)