DisGeNET is a knowledge management platform that integrates and standardizes the data of genes and mutations related to diseases from multiple sources. It covers entire range of human disease.
Source | Last Updated |
---|---|
DisGeNET | July 29, 2024 |
Disease ID | Disease Name | Gene Symbol | Gene ID | Gene Name ▼ | UniProt ID |
---|---|---|---|---|---|
C0025958 | Microcephaly | CAT | 847 | catalase | P04040 |
C0007131 | Non-Small Cell Lung Carcinoma | CAT | 847 | catalase | P04040 |
C0009375 | Colonic Neoplasms | CAT | 847 | catalase | P04040 |
C0520947 | Clumsiness - motor delay | CAT | 847 | catalase | P04040 |
C0205770 | Choroid Plexus Papilloma | CAT | 847 | catalase | P04040 |
C0406810 | Carney Complex | CAT | 847 | catalase | P04040 |
C0917796 | Optic Atrophy, Hereditary, Leber | CAT | 847 | catalase | P04040 |
C0019189 | Hepatitis, Chronic | CAT | 847 | catalase | P04040 |
C0036646 | Age-related cataract | CAT | 847 | catalase | P04040 |
C0162871 | Aortic Aneurysm, Abdominal | CAT | 847 | catalase | P04040 |
C0549473 | Thyroid carcinoma | CAT | 847 | catalase | P04040 |
C0017178 | Gastrointestinal Diseases | CAT | 847 | catalase | P04040 |
C0699885 | Carcinoma of bladder | CAT | 847 | catalase | P04040 |
C1856689 | FRIEDREICH ATAXIA 1 | CAT | 847 | catalase | P04040 |
C0024440 | Macular Edema, Cystoid | CAT | 847 | catalase | P04040 |
C0028754 | Obesity | CAT | 847 | catalase | P04040 |
C0013902 | Elliptocytosis, Hereditary | CAT | 847 | catalase | P04040 |
C0235527 | Heart Failure, Right-Sided | CAT | 847 | catalase | P04040 |
C1565489 | Renal Insufficiency | CAT | 847 | catalase | P04040 |
C0008909 | Claustrophobia | CAT | 847 | catalase | P04040 |
C0919267 | ovarian neoplasm | CAT | 847 | catalase | P04040 |
C0155880 | Intrinsic asthma | CAT | 847 | catalase | P04040 |
C1332206 | Adult Lymphoma | CAT | 847 | catalase | P04040 |
C0947622 | Cholecystolithiasis | CAT | 847 | catalase | P04040 |
C0751039 | Cockayne Syndrome, Type I | CAT | 847 | catalase | P04040 |
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Last updated: August 19, 2024