KEGG Diseases
2,493 diseases | Page 5 / 84
| Disease ID | Disease Name | Multi-Target Proteins | |
|---|---|---|---|
H02525 |
Disorders of innate immunity | 18 | View |
H02170 |
Microphthalmia, syndromic | 18 | View |
H00595 |
Myofibrillar myopathies | 18 | View |
H00021 |
Renal cell carcinoma | 18 | View |
H01740 |
Macrothrombocytopenia | 18 | View |
H01762 |
Muscle glycogen storage disease | 18 | View |
H00801 |
Familial thoracic aortic aneurysm and dissection | 18 | View |
H02310 |
Renal tubular acidosis | 18 | View |
H01355 |
Kearns-Sayre syndrome | 18 | View |
H00779 |
Usher syndrome | 17 | View |
H00100 |
Neutropenic disorders | 17 | View |
H00557 |
Cutis laxa | 17 | View |
H01174 |
Congenital diarrhea | 17 | View |
H00607 |
46,XY gonadal dysgenesis | 17 | View |
H01730 |
Myocardial infarction | 17 | View |
H00261 |
Meckel syndrome | 17 | View |
H00787 |
Congenital stationary night blindness | 17 | View |
H00293 |
Arrhythmogenic right ventricular cardiomyopathy | 16 | View |
H00535 |
Lymphatic malformation | 16 | View |
H00016 |
Oral cancer | 16 | View |
H00810 |
Progressive myoclonic epilepsy | 16 | View |
H00624 |
Progressive familial intrahepatic cholestasis | 16 | View |
H00403 |
Disorders of nucleotide excision repair | 16 | View |
H00149 |
Neuronal ceroid lipofuscinosis | 16 | View |
H00734 |
Autosomal recessive congenital ichthyosis | 16 | View |
H01227 |
Inflammatory bowel disease (IBD) | 16 | View |
H00421 |
Mucopolysaccharidosis | 16 | View |
H00811 |
Distal arthrogryposis | 16 | View |
H00455 |
Spinal muscular atrophy | 16 | View |
H01510 |
Malignant paraganglioma | 16 | View |