KEGG Diseases
2,493 diseases | Page 11 / 84
| Disease ID | Disease Name | Multi-Target Proteins | |
|---|---|---|---|
H00584 |
Epidermolysis bullosa simplex | 9 | View |
H00407 |
Peroxisomal beta-oxidation enzyme deficiency | 9 | View |
H02569 |
Pulmonary fibrosis and/or bone marrow failure, telomere-related | 9 | View |
H00541 |
Autosomal dominant tubulointerstitial kidney disease | 9 | View |
H00107 |
Other well-defined immunodeficiency syndromes | 9 | View |
H01619 |
Primary pulmonary hypertension | 9 | View |
H00094 |
Immunodeficiency associated with DNA repair defects | 9 | View |
H02532 |
Proteasome-associated autoinflammatory syndrome | 9 | View |
H00086 |
Immunodeficiency with hyper-IgM | 9 | View |
H00103 |
Late complement pathway defects | 9 | View |
H00232 |
Hereditary stomatocytosis | 8 | View |
H01513 |
Retinoblastoma | 8 | View |
H01019 |
Catecholaminergic polymorphic ventricular tachycardia | 8 | View |
H02709 |
Neurodevelopmental disorder with aminoacyl-tRNA synthetase defect | 8 | View |
H00737 |
Peeling skin syndrome | 8 | View |
H01210 |
Hypomagnesemia | 8 | View |
H01109 |
Chronic mucocutaneous candidiasis | 8 | View |
H00538 |
Senior-Loken syndrome | 8 | View |
H01209 |
Deafness, X-linked | 8 | View |
H01784 |
Primary hyperchylomicronemia | 8 | View |
H00476 |
Multiple epiphyseal dysplasia | 8 | View |
H00971 |
Achromatopsia | 8 | View |
H00271 |
Polymicrogyria | 8 | View |
H00877 |
Brain small vessel disease | 8 | View |
H01640 |
Uterine leiomyoma | 8 | View |
H01341 |
Collagen VI myopathy | 8 | View |
H01340 |
Bethlem myopathy | 8 | View |
H00479 |
Metaphyseal dysplasias | 8 | View |
H01122 |
Congenital pulmonary alveolar proteinosis | 8 | View |
H02123 |
Celiac disease | 8 | View |