KEGG Diseases
2,493 diseases | Page 1 / 84
| Disease ID | Disease Name | Multi-Target Proteins | |
|---|---|---|---|
H00606 |
Early infantile epileptic encephalopathy | 158 | View |
H01282 |
Spermatogenic failure | 141 | View |
H00527 |
Retinitis pigmentosa | 104 | View |
H00605 |
Deafness, autosomal recessive | 103 | View |
H00266 |
Hereditary spastic paraplegia | 93 | View |
H00773 |
Autosomal dominant intellectual developmental disorder | 91 | View |
H00264 |
Charcot-Marie-Tooth disease | 88 | View |
H00604 |
Deafness, autosomal dominant | 78 | View |
H00294 |
Dilated cardiomyopathy | 77 | View |
H00768 |
Autosomal recessive intellectual developmental disorder | 77 | View |
H00891 |
Combined oxidative phosphorylation deficiency | 73 | View |
H00564 |
Primary ciliary dyskinesia | 69 | View |
H00473 |
Mitochondrial complex I deficiency | 63 | View |
H00020 |
Colorectal cancer | 56 | View |
H01202 |
Cataract | 53 | View |
H00063 |
Spinocerebellar ataxia (SCA) | 52 | View |
H00093 |
Combined immunodeficiency | 50 | View |
H00530 |
Joubert syndrome and related disorders | 50 | View |
H00292 |
Hypertrophic cardiomyopathy | 44 | View |
H00480 |
X-linked intellectual developmental disorder | 44 | View |
H00031 |
Breast cancer | 44 | View |
H01891 |
Autosomal recessive spinocerebellar ataxias | 43 | View |
H00831 |
Primary dystonia | 42 | View |
H01368 |
Cytochrome c oxidase (COX) deficiency | 40 | View |
H00658 |
X-linked syndromic intellectual developmental disorder | 40 | View |
H00058 |
Amyotrophic lateral sclerosis (ALS) | 40 | View |
H00269 |
Primary microcephaly | 39 | View |
H00408 |
Type 1 diabetes mellitus | 38 | View |
H00593 |
Limb-girdle muscular dystrophy | 38 | View |
H00469 |
Mitochondrial DNA depletion syndrome | 38 | View |