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 7226 - 7250 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Gene Name UniProt ID
C3714756 Intellectual Disability SLC2A10 81031 solute carrier family 2 member 10 O95528
C0011847 Diabetes SLC2A10 81031 solute carrier family 2 member 10 O95528
C0011633 Dermatomyositis SLC2A10 81031 solute carrier family 2 member 10 O95528
C0027092 Myopia SLC2A10 81031 solute carrier family 2 member 10 O95528
C0007193 Cardiomyopathy, Dilated SLC2A10 81031 solute carrier family 2 member 10 O95528
C3812396 Chronic idiopathic pulmonary fibrosis SLC2A10 81031 solute carrier family 2 member 10 O95528
C0002940 Aneurysm SLC2A10 81031 solute carrier family 2 member 10 O95528
C0014868 Esophagitis SLC2A10 81031 solute carrier family 2 member 10 O95528
C0344530 Congenital keratoglobus SLC2A10 81031 solute carrier family 2 member 10 O95528
C4707243 Familial thoracic aortic aneurysm and aortic dissection SLC2A10 81031 solute carrier family 2 member 10 O95528
C0017168 Gastroesophageal reflux disease SLC2A10 81031 solute carrier family 2 member 10 O95528
C0600228 Cardiopulmonary Arrest SLC2A10 81031 solute carrier family 2 member 10 O95528
C0019294 Hernia, Inguinal SLC2A10 81031 solute carrier family 2 member 10 O95528
C0206062 Lung Diseases, Interstitial SLC2A10 81031 solute carrier family 2 member 10 O95528
C1855179 CATARACT, ANTERIOR POLAR SLC2A10 81031 solute carrier family 2 member 10 O95528
C0948008 Ischemic stroke SLC2A10 81031 solute carrier family 2 member 10 O95528
C0018790 Cardiac Arrest SLC2A10 81031 solute carrier family 2 member 10 O95528
C0010278 Craniosynostosis SLC2A10 81031 solute carrier family 2 member 10 O95528
C2697932 Loeys-Dietz Syndrome SLC2A10 81031 solute carrier family 2 member 10 O95528
C0003507 Aortic Valve Stenosis SLC2A10 81031 solute carrier family 2 member 10 O95528
C0398738 Leukocyte adhesion deficiency type 1 SLC2A10 81031 solute carrier family 2 member 10 O95528
C0009782 Connective Tissue Diseases SLC2A10 81031 solute carrier family 2 member 10 O95528
C1458155 Mammary Neoplasms SLC2A10 81031 solute carrier family 2 member 10 O95528
C0027059 Myocarditis SLC2A10 81031 solute carrier family 2 member 10 O95528
C0007194 Hypertrophic Cardiomyopathy SLC2A10 81031 solute carrier family 2 member 10 O95528

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Last updated: August 19, 2024