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 |
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DisGeNET | July 29, 2024 |
Disease ID | Disease Name | Gene Symbol ▼ | Gene ID | Gene Name | UniProt ID |
---|---|---|---|---|---|
C0398623 | Thrombophilia | DLD | 1738 | dihydrolipoamide dehydrogenase | P09622 |
C0278595 | Adult Fibrosarcoma | DLD | 1738 | dihydrolipoamide dehydrogenase | P09622 |
C0220981 | Metabolic acidosis | DLD | 1738 | dihydrolipoamide dehydrogenase | P09622 |
C1136033 | Cutaneous Mastocytosis | DLD | 1738 | dihydrolipoamide dehydrogenase | P09622 |
C0152013 | Adenocarcinoma of lung (disorder) | DLD | 1738 | dihydrolipoamide dehydrogenase | P09622 |
C1318544 | M5b Acute differentiated monocytic leukemia | DLD | 1738 | dihydrolipoamide dehydrogenase | P09622 |
C0025500 | Mesothelioma | DLD | 1738 | dihydrolipoamide dehydrogenase | P09622 |
C0030567 | Parkinson Disease | DLD | 1738 | dihydrolipoamide dehydrogenase | P09622 |
C0016667 | Fragile X Syndrome | DLD | 1738 | dihydrolipoamide dehydrogenase | P09622 |
C0085584 | Encephalopathies | DLD | 1738 | dihydrolipoamide dehydrogenase | P09622 |
C0007134 | Renal Cell Carcinoma | DLD | 1738 | dihydrolipoamide dehydrogenase | P09622 |
C0041296 | Tuberculosis | DLD | 1738 | dihydrolipoamide dehydrogenase | P09622 |
C0001418 | Adenocarcinoma | DLD | 1738 | dihydrolipoamide dehydrogenase | P09622 |
C0024115 | Lung diseases | DLD | 1738 | dihydrolipoamide dehydrogenase | P09622 |
C0024776 | Maple Syrup Urine Disease | DLD | 1738 | dihydrolipoamide dehydrogenase | P09622 |
C0376358 | Malignant neoplasm of prostate | DLD | 1738 | dihydrolipoamide dehydrogenase | P09622 |
C0026764 | Multiple Myeloma | DLD | 1738 | dihydrolipoamide dehydrogenase | P09622 |
C0344315 | Depressed mood | DLD | 1738 | dihydrolipoamide dehydrogenase | P09622 |
C0345904 | Malignant neoplasm of liver | DLD | 1738 | dihydrolipoamide dehydrogenase | P09622 |
C0398739 | Congenital disorder of glycosylation, type 2C | DLD | 1738 | dihydrolipoamide dehydrogenase | P09622 |
C0032580 | Adenomatous Polyposis Coli | DLD | 1738 | dihydrolipoamide dehydrogenase | P09622 |
C0497327 | Dementia | DLD | 1738 | dihydrolipoamide dehydrogenase | P09622 |
C0027051 | Myocardial Infarction | DLD | 1738 | dihydrolipoamide dehydrogenase | P09622 |
C0038506 | Stuttering | DLD | 1738 | dihydrolipoamide dehydrogenase | P09622 |
C1857276 | Trichohepatoenteric Syndrome | DLD | 1738 | dihydrolipoamide dehydrogenase | P09622 |
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Last updated: August 19, 2024