KEGG Diseases
2,493 diseases | Page 4 / 84
| Disease ID | Disease Name | Multi-Target Proteins | |
|---|---|---|---|
H01633 |
High blood pressure | 22 | View |
H01738 |
Noonan syndrome | 22 | View |
H02459 |
Syndromic neurodevelopmental disorder | 21 | View |
H01881 |
Complex cortical dysplasia with other brain malformations | 21 | View |
H00088 |
Common variable immunodeficiency | 21 | View |
H02535 |
Neurodevelopmental disorder with dysmorphic facies | 21 | View |
H00083 |
Allograft rejection | 21 | View |
H00423 |
Sphingolipidosis | 21 | View |
H00254 |
Growth hormone deficiency | 21 | View |
H00084 |
Graft-versus-host disease | 21 | View |
H00038 |
Melanoma | 20 | View |
H00525 |
Disorders of mitochondrial fatty-acid oxidation | 20 | View |
H02505 |
Atherosclerosis | 20 | View |
H00630 |
Rheumatoid arthritis | 20 | View |
H00068 |
Leber hereditary optic atrophy | 20 | View |
H00731 |
Atrial fibrillation | 19 | View |
H00786 |
Hypotrichosis | 19 | View |
H00024 |
Prostate cancer | 19 | View |
H00022 |
Bladder cancer | 19 | View |
H01556 |
Meningioma | 19 | View |
H02412 |
Atypical chronic myeloid leukemia | 19 | View |
H02187 |
Spondyloepimetaphyseal dysplasia | 19 | View |
H02111 |
Autism | 19 | View |
H02999 |
Congenital nonspherocytic hemolytic anemia | 19 | View |
H00205 |
Peroxisome biogenesis disorder | 19 | View |
H00236 |
Congenital polycythemia | 18 | View |
H00808 |
Idiopathic generalized epilepsies | 18 | View |
H01027 |
Microphthalmia | 18 | View |
H01431 |
Cushing syndrome | 18 | View |
H00025 |
Penile cancer | 18 | View |