KEGG Diseases
2,493 diseases | Page 10 / 84
| Disease ID | Disease Name | Multi-Target Proteins | |
|---|---|---|---|
H00999 |
Coenzyme Q10 deficiency | 9 | View |
H00590 |
Congenital muscular dystrophies (CMD/MDC) | 9 | View |
H00047 |
Gallbladder cancer | 9 | View |
H00040 |
Squamous cell carcinoma | 9 | View |
H02424 |
Primary central nervous system lymphoma | 9 | View |
H00842 |
Epidermodysplasia verruciformis | 9 | View |
H00419 |
Congenital generalized lipodystrophy | 9 | View |
H01960 |
Muscular dystrophy-dystroglycanopathy type B | 9 | View |
H02217 |
Juvenile myoclonic epilepsy | 9 | View |
H01677 |
Congenital hydrocephalus | 9 | View |
H01611 |
Alcohol dependence | 9 | View |
H02185 |
Spondylometaphyseal dysplasia | 9 | View |
H01778 |
Ullrich disease | 9 | View |
H00070 |
Galactosemia | 9 | View |
H00586 |
Epidermolysis bullosa, junctional | 9 | View |
H01198 |
Fanconi renotubular syndrome | 9 | View |
H00982 |
Sideroblastic anemia | 9 | View |
H00098 |
Chronic granulomatous disease | 9 | View |
H00216 |
Congenital adrenal hyperplasia | 9 | View |
H00106 |
Complement regulatory protein defects | 9 | View |
H02534 |
Y-linked spermatogenic failure | 9 | View |
H02299 |
Arthrogryposis multiplex congenita | 9 | View |
H00072 |
Pyruvate dehydrogenase complex deficiency | 9 | View |
H00422 |
Glycoproteinoses | 9 | View |
H00458 |
Syndromic craniosynostoses | 9 | View |
H01554 |
Fallopian tube cancer | 9 | View |
H01006 |
Hereditary angioedema | 9 | View |
H00825 |
Familial flecked retina syndrome | 9 | View |
H02339 |
Auditory neuropathy | 9 | View |
H00041 |
Kaposi sarcoma | 9 | View |