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 |
---|---|---|---|---|---|
C0017636 | Glioblastoma | DLD | 1738 | dihydrolipoamide dehydrogenase | P09622 |
C0023418 | leukemia | DLD | 1738 | dihydrolipoamide dehydrogenase | P09622 |
C0020538 | Hypertensive disease | DLD | 1738 | dihydrolipoamide dehydrogenase | P09622 |
C0038454 | Cerebrovascular accident | DLD | 1738 | dihydrolipoamide dehydrogenase | P09622 |
C0021051 | Immunologic Deficiency Syndromes | DLD | 1738 | dihydrolipoamide dehydrogenase | P09622 |
C0338106 | Adenocarcinoma of colon | DLD | 1738 | dihydrolipoamide dehydrogenase | P09622 |
C0011570 | Mental Depression | DLD | 1738 | dihydrolipoamide dehydrogenase | P09622 |
C0011849 | Diabetes Mellitus | DLD | 1738 | dihydrolipoamide dehydrogenase | P09622 |
C1306459 | Primary malignant neoplasm | DLD | 1738 | dihydrolipoamide dehydrogenase | P09622 |
C0282577 | Congenital Disorders of Glycosylation | DLD | 1738 | dihydrolipoamide dehydrogenase | P09622 |
C1319315 | Adenocarcinoma of large intestine | DLD | 1738 | dihydrolipoamide dehydrogenase | P09622 |
C0002395 | Alzheimer's Disease | DLD | 1738 | dihydrolipoamide dehydrogenase | P09622 |
C0007758 | Cerebellar Ataxia | DLD | 1738 | dihydrolipoamide dehydrogenase | P09622 |
C0025637 | Methemoglobinemia | DLD | 1738 | dihydrolipoamide dehydrogenase | P09622 |
C0001430 | Adenoma | DLD | 1738 | dihydrolipoamide dehydrogenase | P09622 |
C0036572 | Seizures | DLD | 1738 | dihydrolipoamide dehydrogenase | P09622 |
C0016719 | Friedreich Ataxia | DLD | 1738 | dihydrolipoamide dehydrogenase | P09622 |
C0016057 | Fibrosarcoma | DLD | 1738 | dihydrolipoamide dehydrogenase | P09622 |
C0684249 | Carcinoma of lung | DLD | 1738 | dihydrolipoamide dehydrogenase | P09622 |
C0023264 | Leigh Disease | DLD | 1738 | dihydrolipoamide dehydrogenase | P09622 |
C0018801 | Heart failure | DLD | 1738 | dihydrolipoamide dehydrogenase | P09622 |
C0025958 | Microcephaly | DLD | 1738 | dihydrolipoamide dehydrogenase | P09622 |
C0040015 | Thrombasthenia | DLD | 1738 | dihydrolipoamide dehydrogenase | P09622 |
C0342783 | Deficiency of butyryl-CoA dehydrogenase | DLD | 1738 | dihydrolipoamide dehydrogenase | P09622 |
C0235480 | Paroxysmal atrial fibrillation | DLD | 1738 | dihydrolipoamide dehydrogenase | P09622 |
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Last updated: August 19, 2024