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 |
---|---|---|---|---|---|
C0018780 | Hearing Loss, High-Frequency | CAT | 847 | catalase | P04040 |
C0003873 | Rheumatoid Arthritis | CAT | 847 | catalase | P04040 |
C0003949 | Asbestosis | CAT | 847 | catalase | P04040 |
C0282526 | Hyperpipecolic Acidemia | CAT | 847 | catalase | P04040 |
C0036202 | Sarcoidosis | CAT | 847 | catalase | P04040 |
C1561643 | Chronic Kidney Diseases | CAT | 847 | catalase | P04040 |
C0022665 | Kidney Neoplasm | CAT | 847 | catalase | P04040 |
C3875321 | Inflammatory dermatosis | CAT | 847 | catalase | P04040 |
C0004943 | Behcet Syndrome | CAT | 847 | catalase | P04040 |
C0001973 | Alcoholic Intoxication, Chronic | CAT | 847 | catalase | P04040 |
C0027819 | Neuroblastoma | CAT | 847 | catalase | P04040 |
C1269683 | Major Depressive Disorder | CAT | 847 | catalase | P04040 |
C2711227 | Steatohepatitis | CAT | 847 | catalase | P04040 |
C0029882 | Otitis Media | CAT | 847 | catalase | P04040 |
C0038354 | Stomach Diseases | CAT | 847 | catalase | P04040 |
C0010054 | Coronary Arteriosclerosis | CAT | 847 | catalase | P04040 |
C0282527 | Infantile Refsum Disease (disorder) | CAT | 847 | catalase | P04040 |
C0086795 | Pfaundler-Hurler Syndrome | CAT | 847 | catalase | P04040 |
C0027022 | Myeloproliferative disease | CAT | 847 | catalase | P04040 |
C0022610 | Kernicterus | CAT | 847 | catalase | P04040 |
C0282525 | Adrenoleukodystrophy, Neonatal | CAT | 847 | catalase | P04040 |
C0043208 | Wolman Disease | CAT | 847 | catalase | P04040 |
C3714636 | Pneumonitis | CAT | 847 | catalase | P04040 |
C0043119 | Werner Syndrome | CAT | 847 | catalase | P04040 |
C0014070 | Encephalomyelitis | CAT | 847 | catalase | P04040 |
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Last updated: August 19, 2024