UniProtKB 66,283 results
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UniProtKB Entries
Keyword
- 66,283Top level
- 3,447DiseaseKeyword ID:KW-9995
- 12Age-related macular degeneration<1%
- 8Aicardi-Goutieres syndrome<1%
- 93AIDS2%
- 7Albinism<1%
- 170Allergen3%
- 4Alport syndrome<1%
- 16Alzheimer disease<1%
- 8Amelogenesis imperfecta<1%
- 26Amyloidosis<1%
- 8Aortic aneurysm<1%
- 8Asthma<1%
- 5Atherosclerosis<1%
- 12Atrial fibrillation<1%
- 5Atrial septal defect<1%
- 43Autism spectrum disorder1%
- 10Brugada syndrome<1%
- 72Cardiomyopathy1%
- 53Cataract1%
- 6Chronic granulomatous disease<1%
- 83Ciliopathy1%
- 6Cockayne syndrome<1%
- 11Cone-rod dystrophy<1%
- 5Congenital adrenal hyperplasia<1%
- 20Congenital disorder of glycosylation<1%
- 6Congenital erythrocytosis<1%
- 10Congenital hypothyroidism<1%
- 15Congenital muscular dystrophy<1%
- 14Congenital myasthenic syndrome<1%
- 12Corneal dystrophy<1%
- 19Craniosynostosis<1%
- 8Crown gall tumor<1%
- 6Cushing syndrome<1%
- 163Deafness3%
- 5Dental caries<1%
- 57Diabetes mellitus1%
- 18Diamond-Blackfan anemia<1%
- 2,483Disease variant40%
- 138Dwarfism2%
- 13Dyskeratosis congenita<1%
- 31Dystonia1%
- 7Dystroglycanopathy<1%
- 38Ectodermal dysplasia1%
- 11Ehlers-Danlos syndrome<1%
- 5Emery-Dreifuss muscular dystrophy<1%
- 7Epidermolysis bullosa<1%
- 209Epilepsy3%
- 21Fanconi anemia<1%
- 5Gangliosidosis<1%
- 10Glaucoma<1%
- 15Glycogen storage disease<1%
- 7Hemolytic uremic syndrome<1%
- 31Hereditary hemolytic anemia1%
- 7Hereditary nonpolyposis colorectal cancer<1%
- 8Heterotaxy<1%
- 9Hirschsprung disease<1%
- 7Holoprosencephaly<1%
- 18Hypogonadotropic hypogonadism<1%
- 20Hypotrichosis<1%
- 27Ichthyosis<1%
- 511Intellectual disability8%
- 9Intrahepatic cholestasis<1%
- 11Kallmann syndrome<1%
- 14Leber congenital amaurosis<1%
- 33Leukodystrophy1%
- 25Limb-girdle muscular dystrophy<1%
- 24Lissencephaly<1%
- 12Long QT syndrome<1%
- 29Malaria<1%
- 14Microphthalmia<1%
- 12Mucopolysaccharidosis<1%
- 8Myofibrillar myopathy<1%
- 5Nemaline myopathy<1%
- 12Nephronophthisis<1%
- 286Neurodegeneration5%
- 99Neuropathy2%
- 42Obesity1%
- 63Oncogene1%
- 10Osteogenesis imperfecta<1%
- 10Osteopetrosis<1%
- 9Osteoporosis<1%
- 21Palmoplantar keratoderma<1%
- 18Parkinson disease<1%
- 32Parkinsonism1%
- 7Peroxisome biogenesis disorder<1%
- 5Phenylketonuria<1%
- 11Premature ovarian failure<1%
- 5Primary hypomagnesemia<1%
- 25Primary microcephaly<1%
- 127Primary mitochondrial disease2%
- 203Proto-oncogene3%
- 6Pseudohermaphroditism<1%
- 58Retinitis pigmentosa1%
- 13Schizophrenia<1%
- 17SCID<1%
- 20Systemic lupus erythematosus<1%
- 10Thrombophilia<1%
- 164Tumor suppressor3%
- 7Whooping cough<1%
- 15Williams-Beuren syndrome<1%
- 9Xeroderma pigmentosum<1%