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 15851 - 15875 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▲
C0042769 Virus Diseases DLD 1738 dihydrolipoamide dehydrogenase P09622
C0011860 Diabetes Mellitus, Non-Insulin-Dependent DLD 1738 dihydrolipoamide dehydrogenase P09622
C0476254 Dyslexia DLD 1738 dihydrolipoamide dehydrogenase P09622
C0011265 Presenile dementia DLD 1738 dihydrolipoamide dehydrogenase P09622
C0236642 Pick Disease of the Brain DLD 1738 dihydrolipoamide dehydrogenase P09622
C0220994 Hyperammonemia DLD 1738 dihydrolipoamide dehydrogenase P09622
C0600139 Prostate carcinoma DLD 1738 dihydrolipoamide dehydrogenase P09622
C3554657 LISSENCEPHALY 5 DLD 1738 dihydrolipoamide dehydrogenase P09622
C0036341 Schizophrenia DLD 1738 dihydrolipoamide dehydrogenase P09622
C0024623 Malignant neoplasm of stomach DLD 1738 dihydrolipoamide dehydrogenase P09622
C0020456 Hyperglycemia DLD 1738 dihydrolipoamide dehydrogenase P09622
C0009375 Colonic Neoplasms DLD 1738 dihydrolipoamide dehydrogenase P09622
C0010346 Crohn Disease LCT 3938 lactase P09848
C0311370 Lupus anticoagulant disorder LCT 3938 lactase P09848
C1857231 LACTASE PERSISTENCE LCT 3938 lactase P09848
C0022951 Lactose Intolerance LCT 3938 lactase P09848
C0268181 Lactose Intolerance, Adult Type LCT 3938 lactase P09848
C0028754 Obesity LCT 3938 lactase P09848
C1956346 Coronary Artery Disease LCT 3938 lactase P09848
C0524620 Metabolic Syndrome X LCT 3938 lactase P09848
C0006826 Malignant Neoplasms LCT 3938 lactase P09848
C0432306 Ichthyosis Bullosa of Siemens LCT 3938 lactase P09848
C0036341 Schizophrenia LCT 3938 lactase P09848
C0027651 Neoplasms LCT 3938 lactase P09848
C0032580 Adenomatous Polyposis Coli LCT 3938 lactase P09848

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Last updated: August 19, 2024