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 |
---|---|---|---|---|---|
C0018817 | Atrial Septal Defects | CAT | 847 | catalase | P04040 |
C1844376 | Granulomatous Disease, Chronic, X-Linked | CAT | 847 | catalase | P04040 |
C0271680 | Diabetic Polyneuropathies | CAT | 847 | catalase | P04040 |
C0018802 | Congestive heart failure | CAT | 847 | catalase | P04040 |
C0011570 | Mental Depression | CAT | 847 | catalase | P04040 |
C2936847 | Acatalasemia Japanese type | CAT | 847 | catalase | P04040 |
C0011860 | Diabetes Mellitus, Non-Insulin-Dependent | CAT | 847 | catalase | P04040 |
C0029134 | Optic Neuritis | CAT | 847 | catalase | P04040 |
C0302592 | Cervix carcinoma | CAT | 847 | catalase | P04040 |
C0029456 | Osteoporosis | CAT | 847 | catalase | P04040 |
C3714756 | Intellectual Disability | CAT | 847 | catalase | P04040 |
C0022593 | Keratosis | CAT | 847 | catalase | P04040 |
C0011644 | Scleroderma | CAT | 847 | catalase | P04040 |
C1863999 | Peroxisome Biogenesis Disorder, Complementation Group D | CAT | 847 | catalase | P04040 |
C0043346 | Xeroderma Pigmentosum | CAT | 847 | catalase | P04040 |
C0016053 | Fibromyalgia | CAT | 847 | catalase | P04040 |
C0524620 | Metabolic Syndrome X | CAT | 847 | catalase | P04040 |
C0005283 | beta Thalassemia | CAT | 847 | catalase | P04040 |
C0270844 | Tonic Seizures | CAT | 847 | catalase | P04040 |
C0751495 | Seizures, Focal | CAT | 847 | catalase | P04040 |
C4721610 | Carcinoma, Ovarian Epithelial | CAT | 847 | catalase | P04040 |
C0155626 | Acute myocardial infarction | CAT | 847 | catalase | P04040 |
C0239946 | Fibrosis, Liver | CAT | 847 | catalase | P04040 |
C0002395 | Alzheimer's Disease | CAT | 847 | catalase | P04040 |
C0025202 | melanoma | CAT | 847 | catalase | P04040 |
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Last updated: August 19, 2024