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 |
---|---|---|---|---|---|
C0004153 | Atherosclerosis | DCN | 1634 | decorin | P07585 |
C3714756 | Intellectual Disability | DCN | 1634 | decorin | P07585 |
C0476089 | Endometrial Carcinoma | DCN | 1634 | decorin | P07585 |
C4721509 | Usual Interstitial Pneumonia | DCN | 1634 | decorin | P07585 |
C0265274 | Achondrogenesis, type IB (disorder) | DCN | 1634 | decorin | P07585 |
C0376358 | Malignant neoplasm of prostate | DCN | 1634 | decorin | P07585 |
C1263858 | Muscular dystrophy congenital, merosin negative | DCN | 1634 | decorin | P07585 |
C0042373 | Vascular Diseases | DCN | 1634 | decorin | P07585 |
C1800706 | Idiopathic Pulmonary Fibrosis | DCN | 1634 | decorin | P07585 |
C0206650 | Fibroadenoma | DCN | 1634 | decorin | P07585 |
C0085786 | Hamman-Rich syndrome | DCN | 1634 | decorin | P07585 |
C0001080 | Achondroplasia | DCN | 1634 | decorin | P07585 |
C0007820 | Cerebrovascular Disorders | DCN | 1634 | decorin | P07585 |
C0007097 | Carcinoma | DCN | 1634 | decorin | P07585 |
C0024796 | Marfan Syndrome | DCN | 1634 | decorin | P07585 |
C0043119 | Werner Syndrome | DCN | 1634 | decorin | P07585 |
C0151744 | Myocardial Ischemia | DCN | 1634 | decorin | P07585 |
C4048328 | cervical cancer | DCN | 1634 | decorin | P07585 |
C0007102 | Malignant tumor of colon | DCN | 1634 | decorin | P07585 |
C0003850 | Arteriosclerosis | DCN | 1634 | decorin | P07585 |
C1568272 | Tendinopathy | DCN | 1634 | decorin | P07585 |
C0009207 | Cockayne Syndrome | DCN | 1634 | decorin | P07585 |
C2711227 | Steatohepatitis | DCN | 1634 | decorin | P07585 |
C0010495 | Cutis Laxa | DCN | 1634 | decorin | P07585 |
C0036421 | Systemic Scleroderma | DCN | 1634 | decorin | P07585 |
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Last updated: August 19, 2024