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 11526 - 11550 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Gene Name UniProt ID
C0042373 Vascular Diseases DLAT 1737 dihydrolipoamide S-acetyltransferase P10515
C0038013 Ankylosing spondylitis DLAT 1737 dihydrolipoamide S-acetyltransferase P10515
C0003857 Congenital arteriovenous malformation DLAT 1737 dihydrolipoamide S-acetyltransferase P10515
C2239176 Liver carcinoma DLAT 1737 dihydrolipoamide S-acetyltransferase P10515
C0020981 Angioimmunoblastic Lymphadenopathy DLAT 1737 dihydrolipoamide S-acetyltransferase P10515
C0023467 Leukemia, Myelocytic, Acute DLAT 1737 dihydrolipoamide S-acetyltransferase P10515
C0033860 Psoriasis DLAT 1737 dihydrolipoamide S-acetyltransferase P10515
C0678222 Breast Carcinoma DLAT 1737 dihydrolipoamide S-acetyltransferase P10515
C0021400 Influenza DLAT 1737 dihydrolipoamide S-acetyltransferase P10515
C0025958 Microcephaly DLAT 1737 dihydrolipoamide S-acetyltransferase P10515
C0271270 Oculovestibuloauditory syndrome DLAT 1737 dihydrolipoamide S-acetyltransferase P10515
C0011849 Diabetes Mellitus DLAT 1737 dihydrolipoamide S-acetyltransferase P10515
C0004364 Autoimmune Diseases DLAT 1737 dihydrolipoamide S-acetyltransferase P10515
C0036421 Systemic Scleroderma DLAT 1737 dihydrolipoamide S-acetyltransferase P10515
C0019158 Hepatitis DLAT 1737 dihydrolipoamide S-acetyltransferase P10515
C1527336 Sjogren's Syndrome DLAT 1737 dihydrolipoamide S-acetyltransferase P10515
C1168401 Squamous cell carcinoma of the head and neck DLAT 1737 dihydrolipoamide S-acetyltransferase P10515
C0015934 Fetal Growth Retardation DLAT 1737 dihydrolipoamide S-acetyltransferase P10515
C0085859 Polyglandular Type I Autoimmune Syndrome DLAT 1737 dihydrolipoamide S-acetyltransferase P10515
C0151744 Myocardial Ischemia DLAT 1737 dihydrolipoamide S-acetyltransferase P10515
C2748536 Leukocyte Adhesion Deficiency, Type III DLD 1738 dihydrolipoamide dehydrogenase P09622
C0272187 Congenital leukocyte adherence deficiency DLD 1738 dihydrolipoamide dehydrogenase P09622
C0009460 Communication impairment DLD 1738 dihydrolipoamide dehydrogenase P09622
C0007102 Malignant tumor of colon DLD 1738 dihydrolipoamide dehydrogenase P09622
C0699791 Stomach Carcinoma DLD 1738 dihydrolipoamide dehydrogenase P09622

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Last updated: August 19, 2024