KEGG Diseases
2,493 diseases | Page 8 / 84
| Disease ID | Disease Name | Multi-Target Proteins | |
|---|---|---|---|
H00108 |
Autoimmune lymphoproliferative syndromes | 12 | View |
H02086 |
Mitochondrial complex III deficiency | 12 | View |
H00168 |
Oculocutaneous albinism | 12 | View |
H01428 |
Xeroderma pigmentosum | 12 | View |
H00512 |
Permanent neonatal diabetes mellitus | 12 | View |
H01760 |
Hepatic glycogen storage disease | 12 | View |
H00625 |
Tooth agenesis | 12 | View |
H02049 |
Bilateral macronodular adrenal hyperplasia | 12 | View |
H00243 |
Renal tubular acidosis type 4 | 12 | View |
H00664 |
Anemia due to disorders of glycolytic enzymes | 12 | View |
H01621 |
Pulmonary arterial hypertension | 12 | View |
H01369 |
ATP synthase deficiency | 12 | View |
H02036 |
Combined pituitary hormone deficiency | 12 | View |
H01222 |
Cowden syndrome | 11 | View |
H01398 |
Primary hyperammonemia (Urea cycle disorders) | 11 | View |
H00033 |
Adrenal carcinoma | 11 | View |
H00004 |
Chronic myeloid leukemia | 11 | View |
H00046 |
Cholangiocarcinoma | 11 | View |
H00054 |
Nasopharyngeal cancer | 11 | View |
H02803 |
Neurodevelopmental disorder with histone modification defect | 11 | View |
H01351 |
Spastic ataxia | 11 | View |
H00239 |
Bartter syndrome | 11 | View |
H01216 |
Left ventricular noncompaction | 11 | View |
H01118 |
Progressive external ophthalmoplegia | 11 | View |
H01593 |
Osteoporosis | 11 | View |
H02481 |
Syndromic disorder with short stature | 11 | View |
H00549 |
Tetralogy of Fallot | 11 | View |
H00542 |
Polycystic kidney disease | 11 | View |
H02041 |
Myopia | 11 | View |
H00251 |
Thyroid dyshormonogenesis | 11 | View |