KEGG Diseases
2,493 diseases | Page 6 / 84
| Disease ID | Disease Name | Multi-Target Proteins | |
|---|---|---|---|
H00223 |
Inherited thrombophilia | 16 | View |
H00085 |
Agammaglobulinemias | 16 | View |
H00177 |
Neonatal adrenoleukodystrophy | 16 | View |
H01342 |
Zellweger syndrome | 16 | View |
H00632 |
Heterotaxy | 15 | View |
H00865 |
Lethal congenital contractural syndrome | 15 | View |
H01020 |
Optic atrophy | 15 | View |
H00268 |
Lissencephaly | 15 | View |
H00436 |
Osteopetrosis | 15 | View |
H02685 |
Developmental delay with neuropsychiatric disorders | 15 | View |
H00166 |
Hermansky-Pudlak syndrome | 15 | View |
H02529 |
Bone marrow failure syndrome | 15 | View |
H00028 |
Choriocarcinoma | 15 | View |
H00026 |
Endometrial cancer | 15 | View |
H01705 |
Bilateral sudden sensorineural hearing loss | 15 | View |
H00454 |
Oral-facial-digital syndrome | 15 | View |
H00010 |
Multiple myeloma | 15 | View |
H00102 |
Classic complement pathway component defects | 15 | View |
H00594 |
Distal myopathy | 14 | View |
H02301 |
Nephroblastoma | 14 | View |
H01463 |
Mycosis fungoides | 14 | View |
H00120 |
Muscular dystrophy-dystroglycanopathy type A | 14 | View |
H02307 |
Muscular dystrophy-dystroglycanopathy | 14 | View |
H02132 |
Microcephaly syndrome | 14 | View |
H00420 |
Familial partial lipodystrophy | 14 | View |
H01574 |
Familial idiopathic basal ganglia calcification | 14 | View |
H00089 |
IFN-gamma/IL-12 axis | 14 | View |
H00626 |
Focal segmental glomerulosclerosis | 14 | View |
H01267 |
Familial hyperinsulinemic hypoglycemia | 14 | View |
H01102 |
Pituitary adenomas | 13 | View |