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
Displaying entries 51126 - 51150 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Gene Name UniProt ID
C0342783 Deficiency of butyryl-CoA dehydrogenase DLD 1738 dihydrolipoamide dehydrogenase P09622
C0235480 Paroxysmal atrial fibrillation DLD 1738 dihydrolipoamide dehydrogenase P09622
C0242231 Coronary Stenosis DLD 1738 dihydrolipoamide dehydrogenase P09622
C0013421 Dystonia DLD 1738 dihydrolipoamide dehydrogenase P09622
C3714756 Intellectual Disability DLD 1738 dihydrolipoamide dehydrogenase P09622
C0018802 Congestive heart failure DLD 1738 dihydrolipoamide dehydrogenase P09622
C0019151 Hepatic Encephalopathy DLD 1738 dihydrolipoamide dehydrogenase P09622
C0025517 Metabolic Diseases DLD 1738 dihydrolipoamide dehydrogenase P09622
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

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Last updated: August 19, 2024