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 43451 - 43475 of 62743 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Gene Name UniProt ID
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
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

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Last updated: August 19, 2024