KEGG Diseases
2,493 diseases | Page 3 / 84
| Disease ID | Disease Name | Multi-Target Proteins | |
|---|---|---|---|
H01563 |
HIV infection | 28 | View |
H00481 |
Cone-rod dystrophy and cone dystrophy | 28 | View |
H01489 |
Inherited glycosylphosphatidylinositol deficiencies | 27 | View |
H02410 |
Myelodysplastic/myeloproliferative neoplasms | 27 | View |
H00897 |
Pontocerebellar hypoplasia | 27 | View |
H00770 |
Congenital myasthenic syndrome | 27 | View |
H00615 |
Amelogenesis imperfecta | 26 | View |
H00720 |
Long QT syndrome | 26 | View |
H00042 |
Glioma | 26 | View |
H00014 |
Non-small cell lung cancer | 26 | View |
H00410 |
Maturity onset diabetes of the young (MODY) | 26 | View |
H00409 |
Type 2 diabetes mellitus | 26 | View |
H00537 |
Nephronophthisis | 26 | View |
H01897 |
Oocyte/zygote/embryo maturation arrest | 26 | View |
H00237 |
Diamond-Blackfan anemia | 26 | View |
H02470 |
Neurodevelopmental disorder with structural brain abnormalities | 26 | View |
H00027 |
Ovarian cancer | 26 | View |
H01725 |
Primary immunodeficiency disease | 25 | View |
H02715 |
Neurodevelopmental disorder with defects of ubiquitin-proteasome system | 25 | View |
H00017 |
Esophageal cancer | 25 | View |
H00342 |
Tuberculosis | 25 | View |
H02411 |
Chronic myelomonocytic leukemia | 25 | View |
H00265 |
Hereditary sensory and autonomic neuropathy | 23 | View |
H02157 |
Short-rib thoracic dysplasia | 23 | View |
H00361 |
Malaria | 23 | View |
H00523 |
Noonan syndrome and related disorders | 23 | View |
H00978 |
Thrombocytopenia (THC) | 22 | View |
H01235 |
Bleeding disorder platelet-type | 22 | View |
H00019 |
Pancreatic cancer | 22 | View |
H02461 |
Neurodevelopmental disorder with microcephaly | 22 | View |