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Glycan Structure Repository
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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 |
|---|---|---|---|---|---|
| C0022333 | Jacksonian Seizure | CAT | 847 | catalase | P04040 |
| C0020473 | Hyperlipidemia | CAT | 847 | catalase | P04040 |
| C0003165 | Anthracosis | CAT | 847 | catalase | P04040 |
| C0079731 | B-Cell Lymphomas | CAT | 847 | catalase | P04040 |
| C0042109 | Urticaria | CAT | 847 | catalase | P04040 |
| C0010068 | Coronary heart disease | CAT | 847 | catalase | P04040 |
| C0002726 | Amyloidosis | CAT | 847 | catalase | P04040 |
| C0015625 | Fanconi Anemia | CAT | 847 | catalase | P04040 |
| C1848934 | SPONDYLOCARPOTARSAL SYNOSTOSIS SYNDROME | CAT | 847 | catalase | P04040 |
| C0024141 | Lupus Erythematosus, Systemic | CAT | 847 | catalase | P04040 |
| C0206664 | Teratocarcinoma | CAT | 847 | catalase | P04040 |
| C0023860 | Listeriosis | CAT | 847 | catalase | P04040 |
| C0270824 | Visual seizure | CAT | 847 | catalase | P04040 |
| C0740391 | Middle Cerebral Artery Occlusion | CAT | 847 | catalase | P04040 |
| C0021364 | Male infertility | CAT | 847 | catalase | P04040 |
| C0010495 | Cutis Laxa | CAT | 847 | catalase | P04040 |
| C1636149 | Macular dystrophy, corneal type 1 | CAT | 847 | catalase | P04040 |
| C0268790 | Renal vascular disorder | CAT | 847 | catalase | P04040 |
| C0007789 | Cerebral Palsy | CAT | 847 | catalase | P04040 |
| C0011854 | Diabetes Mellitus, Insulin-Dependent | CAT | 847 | catalase | P04040 |
| C0019348 | Herpes Simplex Infections | CAT | 847 | catalase | P04040 |
| C0035344 | Retinopathy of Prematurity | CAT | 847 | catalase | P04040 |
| C1861172 | Venous Thromboembolism | CAT | 847 | catalase | P04040 |
| C0023493 | Adult T-Cell Lymphoma/Leukemia | CAT | 847 | catalase | P04040 |
| C3539168 | PEROXISOME BIOGENESIS DISORDER, COMPLEMENTATION GROUP A | CAT | 847 | catalase | P04040 |
