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DisGeNET
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 |
|---|---|---|---|---|---|
| C0035309 | Retinal Diseases | CAT | 847 | catalase | P04040 |
| C0004509 | Azoospermia | CAT | 847 | catalase | P04040 |
| C0021670 | insulinoma | CAT | 847 | catalase | P04040 |
| C0751434 | Classical phenylketonuria | CAT | 847 | catalase | P04040 |
| C0019202 | Hepatolenticular Degeneration | CAT | 847 | catalase | P04040 |
| C0017636 | Glioblastoma | CAT | 847 | catalase | P04040 |
| C0001815 | Primary Myelofibrosis | CAT | 847 | catalase | P04040 |
| C0033575 | Prostatic Diseases | CAT | 847 | catalase | P04040 |
| C0004364 | Autoimmune Diseases | CAT | 847 | catalase | P04040 |
| C0024623 | Malignant neoplasm of stomach | CAT | 847 | catalase | P04040 |
| C1862389 | ATRIAL SEPTAL DEFECT 1 | CAT | 847 | catalase | P04040 |
| C0019061 | Hemolytic-Uremic Syndrome | CAT | 847 | catalase | P04040 |
| C0206624 | Hepatoblastoma | CAT | 847 | catalase | P04040 |
| C0002871 | Anemia | CAT | 847 | catalase | P04040 |
| C0917798 | Cerebral Ischemia | CAT | 847 | catalase | P04040 |
| C0598608 | Hyperhomocysteinemia | CAT | 847 | catalase | P04040 |
| C3714618 | Primary Hyperthyroidism | CAT | 847 | catalase | P04040 |
| C0006413 | Burkitt Lymphoma | CAT | 847 | catalase | P04040 |
| C0017152 | Gastritis | CAT | 847 | catalase | P04040 |
| C0018081 | Gonorrhea | CAT | 847 | catalase | P04040 |
| C0032285 | Pneumonia | CAT | 847 | catalase | P04040 |
| C4082937 | Necrotizing enterocolitis in fetus OR newborn | CAT | 847 | catalase | P04040 |
| C0020550 | Hyperthyroidism | CAT | 847 | catalase | P04040 |
| C0043459 | Zellweger Syndrome | CAT | 847 | catalase | P04040 |
| C1527168 | Bonnevie-Ullrich Syndrome | CAT | 847 | catalase | P04040 |
