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 54101 - 54125 of 62743 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Gene Name UniProt ID
C0017152 Gastritis SELL 6402 selectin L P14151
C0017658 Glomerulonephritis SELL 6402 selectin L P14151
C0021400 Influenza SELL 6402 selectin L P14151
C0024117 Chronic Obstructive Airway Disease SELL 6402 selectin L P14151
C1306459 Primary malignant neoplasm SELL 6402 selectin L P14151
C1306759 Eosinophilic disorder SELL 6402 selectin L P14151
C0022661 Kidney Failure, Chronic SELL 6402 selectin L P14151
C0742343 Acute Chest Syndrome SELL 6402 selectin L P14151
C0007570 Celiac Disease SELL 6402 selectin L P14151
C0021390 Inflammatory Bowel Diseases SELL 6402 selectin L P14151
C0205647 Follicular adenoma SELL 6402 selectin L P14151
C0031090 Periodontal Diseases SELL 6402 selectin L P14151
C2239176 Liver carcinoma SELL 6402 selectin L P14151
C0243026 Sepsis SELL 6402 selectin L P14151
C0220597 Adult Hodgkin Lymphoma SELL 6402 selectin L P14151
C0079770 Lymphoma, Small Noncleaved-Cell SELL 6402 selectin L P14151
C0023492 Leukemia, T-Cell SELL 6402 selectin L P14151
C0206695 Carcinoma, Neuroendocrine SELL 6402 selectin L P14151
C1850900 Familial primary gastric lymphoma SELL 6402 selectin L P14151
C0022116 Ischemia SELL 6402 selectin L P14151
C1168401 Squamous cell carcinoma of the head and neck SELL 6402 selectin L P14151
C0011847 Diabetes SELL 6402 selectin L P14151
C0014175 Endometriosis SELL 6402 selectin L P14151
C0392514 Hereditary hemochromatosis SELL 6402 selectin L P14151
C0026764 Multiple Myeloma SELL 6402 selectin L P14151

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Last updated: August 19, 2024