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 54151 - 54175 of 62743 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Gene Name UniProt ID
C0003850 Arteriosclerosis SELL 6402 selectin L P14151
C0151744 Myocardial Ischemia SELL 6402 selectin L P14151
C0035078 Kidney Failure SELL 6402 selectin L P14151
C0079293 Epidermolysis Bullosa Acquisita SELL 6402 selectin L P14151
C0005695 Bladder Neoplasm SELL 6402 selectin L P14151
C0031115 Peripheral angiopathy in diseases classified elsewhere SELL 6402 selectin L P14151
C0037116 Silicosis SELL 6402 selectin L P14151
C0948008 Ischemic stroke SELL 6402 selectin L P14151
C0042373 Vascular Diseases SELL 6402 selectin L P14151
C0007102 Malignant tumor of colon SELL 6402 selectin L P14151
C0152013 Adenocarcinoma of lung (disorder) SELP 6403 selectin P P16109
C0040034 Thrombocytopenia SELP 6403 selectin P P16109
C0948008 Ischemic stroke SELP 6403 selectin P P16109
C0027651 Neoplasms SELP 6403 selectin P P16109
C0742343 Acute Chest Syndrome SELP 6403 selectin P P16109
C1306459 Primary malignant neoplasm SELP 6403 selectin P P16109
C0023530 Leukopenia SELP 6403 selectin P P16109
C1956346 Coronary Artery Disease SELP 6403 selectin P P16109
C0004238 Atrial Fibrillation SELP 6403 selectin P P16109
C0027947 Neutropenia SELP 6403 selectin P P16109
C0004153 Atherosclerosis SELP 6403 selectin P P16109
C0018801 Heart failure SELP 6403 selectin P P16109
C0027051 Myocardial Infarction SELP 6403 selectin P P16109
C0017668 Focal glomerulosclerosis SELP 6403 selectin P P16109
C1861172 Venous Thromboembolism SELP 6403 selectin P P16109

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Last updated: August 19, 2024