KEGG Diseases
2,493 diseases | Page 12 / 84
| Disease ID | Disease Name | Multi-Target Proteins | |
|---|---|---|---|
H01742 |
Coronary artery disease | 8 | View |
H00174 |
Methylmalonic aciduria | 8 | View |
H01481 |
Myelodysplastic syndrome | 8 | View |
H00007 |
Hodgkin lymphoma | 8 | View |
H00563 |
Emery-Dreifuss muscular dystrophy | 8 | View |
H00533 |
Hereditary hemorrhagic telangiectasia | 8 | View |
H00845 |
Familial amyloidosis | 8 | View |
H02627 |
Epidermal nevus | 8 | View |
H02541 |
Juvenile myelomonocytic leukemia | 8 | View |
H00631 |
Cornelia de Lange syndrome | 8 | View |
H00598 |
46,XX testicular disorder of sex development | 8 | View |
H00167 |
Phenylketonuria | 8 | View |
H00876 |
Mismatch repair deficiency | 8 | View |
H00183 |
Homocystinuria | 8 | View |
H01413 |
Adams-Oliver syndrome | 8 | View |
H01470 |
Giant cell tumor of bone | 8 | View |
H01490 |
Multiple sclerosis | 8 | View |
H00513 |
Transient neonatal diabetes mellitus | 8 | View |
H01347 |
MELAS syndrome | 8 | View |
H01365 |
Leber hereditary optic neuropathy and dystonia | 8 | View |
H02542 |
Acute promyelocytic leukemia | 8 | View |
H00207 |
Rhizomelic chondrodysplasia punctata | 8 | View |
H00984 |
MHC class I deficiency | 8 | View |
H00039 |
Basal cell carcinoma | 8 | View |
H01612 |
Essential thrombocythemia | 7 | View |
H00493 |
Heparan sulfate proteoglycan gene defects | 7 | View |
H01577 |
Essential tremor | 7 | View |
H00667 |
Woolly hair | 7 | View |
H01464 |
Mantle cell lymphoma | 7 | View |
H00700 |
Centronuclear myopathy | 7 | View |