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 ▲ |
---|---|---|---|---|---|
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 |
C0011875 | Diabetic Angiopathies | CAT | 847 | catalase | P04040 |
C0008350 | Cholelithiasis | CAT | 847 | catalase | P04040 |
C0008370 | Cholestasis | CAT | 847 | catalase | P04040 |
C0021831 | Intestinal Diseases | CAT | 847 | catalase | P04040 |
C0220668 | Congenital contractural arachnodactyly | CAT | 847 | catalase | P04040 |
C0026847 | Spinal Muscular Atrophy | CAT | 847 | catalase | P04040 |
C0015696 | Fatty Liver, Alcoholic | CAT | 847 | catalase | P04040 |
C0752121 | Spinocerebellar Ataxia Type 2 | CAT | 847 | catalase | P04040 |
C0220748 | Cartilage-hair hypoplasia | CAT | 847 | catalase | P04040 |
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Last updated: August 19, 2024