KEGG Diseases
2,493 diseases | Page 2 / 84
| Disease ID | Disease Name | Multi-Target Proteins | |
|---|---|---|---|
H00080 |
Systemic lupus erythematosus | 38 | View |
H01439 |
Williams-Beuren syndrome | 38 | View |
H00119 |
Congenital disorders of glycosylation type II | 37 | View |
H00679 |
Hypomyelinating leukodystrophy | 37 | View |
H00118 |
Congenital disorders of glycosylation type I | 36 | View |
H00627 |
Premature ovarian failure | 36 | View |
H02434 |
Diffuse large B-cell lymphoma, not otherwise specified | 35 | View |
H00018 |
Gastric cancer | 35 | View |
H00856 |
Distal hereditary motor neuropathies | 34 | View |
H02463 |
Syndromic intellectual developmental disorder | 34 | View |
H00255 |
Hypogonadotropic hypogonadism | 33 | View |
H01810 |
Congenital myopathy | 33 | View |
H02397 |
Neurodevelopmental disorder with movement abnormalities or hypotonia | 31 | View |
H02526 |
Disorders of adaptive immunity | 31 | View |
H00032 |
Thyroid cancer | 31 | View |
H02106 |
Genetic obesity | 31 | View |
H00238 |
Fanconi anemia | 30 | View |
H00003 |
Acute myeloid leukemia | 30 | View |
H01657 |
Nephrotic syndrome | 30 | View |
H00418 |
Bardet-Biedl syndrome | 30 | View |
H00048 |
Hepatocellular carcinoma | 29 | View |
H01667 |
Medulloblastoma | 29 | View |
H00506 |
Osteogenesis imperfecta | 29 | View |
H01400 |
Secondary hyperammonemia | 29 | View |
H00069 |
Glycogen storage disease | 29 | View |
H01649 |
Schizophrenia | 28 | View |
H00837 |
Leber congenital amaurosis | 28 | View |
H00821 |
Age-related macular degeneration | 28 | View |
H00057 |
Parkinson disease | 28 | View |
H00079 |
Asthma | 28 | View |