KEGG Diseases
2,493 diseases | Page 14 / 84
| Disease ID | Disease Name | Multi-Target Proteins | |
|---|---|---|---|
H00575 |
Renal tubular dysgenesis | 7 | View |
H00485 |
Robinow syndrome | 7 | View |
H01390 |
Mitochondrial neurogastrointestinal encephalomyopathy | 7 | View |
H00869 |
Leukoencephalopathy with vanishing white matter | 7 | View |
H02160 |
Craniosynostoses | 7 | View |
H00178 |
Glutaric acidemia | 7 | View |
H00484 |
Multiple synostosis syndrome | 7 | View |
H00628 |
Congenital bile acid synthesis defect | 7 | View |
H02221 |
Methylmalonic aciduria and homocystinuria | 7 | View |
H02035 |
Isolated growth hormone deficiency | 7 | View |
H01488 |
Hyperphosphatasia with mental retardation syndrome | 7 | View |
H01396 |
Moyamoya disease | 7 | View |
H01025 |
Familial adenomatous polyposis | 7 | View |
H01132 |
Aplastic anemia | 7 | View |
H00096 |
Defects of toll-like receptor signaling | 7 | View |
H02460 |
Neurodevelopmental disorder with dysmorphic facies and skeletal anomalies | 7 | View |
H00725 |
Short QT syndrome | 7 | View |
H01004 |
Velocardiofacial syndrome | 7 | View |
H01243 |
Huntington disease-like syndrome | 7 | View |
H01605 |
Myelofibrosis | 6 | View |
H02513 |
Oculopharyngodistal myopathy | 6 | View |
H01376 |
Acrofacial dysostosis | 6 | View |
H00008 |
Burkitt lymphoma | 6 | View |
H00009 |
Adult T-cell leukemia | 6 | View |
H01926 |
Ventricular septal defect | 6 | View |
H02214 |
Familial focal epilepsy with variable foci | 6 | View |
H02616 |
Neurodevelopmental disorder with macrocephaly | 6 | View |
H00545 |
Polycystic liver disease | 6 | View |
H00534 |
Cerebral cavernous malformation | 6 | View |
H00529 |
Cranioectodermal dysplasia | 6 | View |