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DisGeNET
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 |
|---|---|---|---|---|---|
| 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 |
| C0878544 | Cardiomyopathies | DLD | 1738 | dihydrolipoamide dehydrogenase | P09622 |
| C0752347 | Lewy Body Disease | DLD | 1738 | dihydrolipoamide dehydrogenase | P09622 |
| C0042373 | Vascular Diseases | DLD | 1738 | dihydrolipoamide dehydrogenase | P09622 |
| C0152132 | Hypertensive Retinopathy | DLD | 1738 | dihydrolipoamide dehydrogenase | P09622 |
| C0338451 | Frontotemporal dementia | DLD | 1738 | dihydrolipoamide dehydrogenase | P09622 |
| C0340319 | Posterior myocardial infarction | DLD | 1738 | dihydrolipoamide dehydrogenase | P09622 |
| C0023903 | Liver neoplasms | DLD | 1738 | dihydrolipoamide dehydrogenase | P09622 |
| C0020615 | Hypoglycemia | DLD | 1738 | dihydrolipoamide dehydrogenase | P09622 |
| C0001125 | Acidosis, Lactic | DLD | 1738 | dihydrolipoamide dehydrogenase | P09622 |
| C1621958 | Glioblastoma Multiforme | DLD | 1738 | dihydrolipoamide dehydrogenase | P09622 |
| C0004352 | Autistic Disorder | DLD | 1738 | dihydrolipoamide dehydrogenase | P09622 |
| C0023014 | Language Development Disorders | DLD | 1738 | dihydrolipoamide dehydrogenase | P09622 |
| C0268120 | Adenine phosphoribosyltransferase deficiency | DLD | 1738 | dihydrolipoamide dehydrogenase | P09622 |
| C0011581 | Depressive disorder | DLD | 1738 | dihydrolipoamide dehydrogenase | P09622 |
| C0751955 | Brain Infarction | DLD | 1738 | dihydrolipoamide dehydrogenase | P09622 |
| C0242379 | Malignant neoplasm of lung | DLD | 1738 | dihydrolipoamide dehydrogenase | P09622 |
| C0002736 | Amyotrophic Lateral Sclerosis | DLD | 1738 | dihydrolipoamide dehydrogenase | P09622 |
| C0009324 | Ulcerative Colitis | DLD | 1738 | dihydrolipoamide dehydrogenase | P09622 |
| C0007194 | Hypertrophic Cardiomyopathy | DLD | 1738 | dihydrolipoamide dehydrogenase | P09622 |
