KEGG Diseases
2,493 diseases | Page 13 / 84
| Disease ID | Disease Name | Multi-Target Proteins | |
|---|---|---|---|
H02213 |
Familial adult myoclonic epilepsy | 7 | View |
H01869 |
Megacystis microcolon intestinal hypoperistalsis syndrome | 7 | View |
H02530 |
Hereditary prostate cancer | 7 | View |
H00917 |
Congenital dyserythropoietic anemia | 7 | View |
H02832 |
Thiamine metabolism dysfunction syndrome | 7 | View |
H00208 |
Hyperbilirubinemia | 7 | View |
H01933 |
Porokeratosis | 7 | View |
H00517 |
Spondylocostal dysostosis | 7 | View |
H02371 |
Intellectual developmental disorder with autism and speech delay | 7 | View |
H01656 |
Psoriasis | 7 | View |
H00933 |
Hereditary pancreatitis | 7 | View |
H01773 |
4p deletion syndrome | 7 | View |
H00201 |
Erythropoietic porphyria | 7 | View |
H00651 |
Hypohidrotic ectodermal dysplasia | 7 | View |
H01208 |
Globozoospermia | 7 | View |
H00807 |
Nocturnal frontal lobe epilepsy | 7 | View |
H00076 |
Cockayne syndrome | 7 | View |
H01635 |
Hyperlipidemia | 7 | View |
H00214 |
Hypophosphatemic rickets | 7 | View |
H00413 |
Hepatitis C | 7 | View |
H01529 |
Avascular necrosis of femoral head | 7 | View |
H02072 |
Stickler syndrome | 7 | View |
H00802 |
Ehlers-Danlos syndrome | 7 | View |
H01307 |
Nonsyndromic congenital nail disorder | 7 | View |
H00202 |
Hepatic porphyria | 7 | View |
H00589 |
Familial exudative vitreoretinopathy | 7 | View |
H00235 |
Methemoglobinemia | 7 | View |
H00172 |
Maple syrup urine disease | 7 | View |
H00045 |
Pancreatic neuroendocrine tumor | 7 | View |
H00044 |
Cancer of the anal canal | 7 | View |