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 53976 - 54000 of 62743 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Gene Name UniProt ID
C0392514 Hereditary hemochromatosis SELE 6401 selectin E P16581
C0035309 Retinal Diseases SELE 6401 selectin E P16581
C0042109 Urticaria SELE 6401 selectin E P16581
C0042373 Vascular Diseases SELE 6401 selectin E P16581
C0009326 Collagen Diseases SELE 6401 selectin E P16581
C0085261 Proteus Syndrome SELE 6401 selectin E P16581
C0024299 Lymphoma SELE 6401 selectin E P16581
C0007131 Non-Small Cell Lung Carcinoma SELE 6401 selectin E P16581
C0023364 Leptospirosis SELE 6401 selectin E P16581
C0011311 Dengue Fever SELE 6401 selectin E P16581
C0751606 Adult Acute Lymphocytic Leukemia SELE 6401 selectin E P16581
C0011884 Diabetic Retinopathy SELE 6401 selectin E P16581
C0021390 Inflammatory Bowel Diseases SELE 6401 selectin E P16581
C0011265 Presenile dementia SELE 6401 selectin E P16581
C0019100 Severe Dengue SELE 6401 selectin E P16581
C0346647 Malignant neoplasm of pancreas SELE 6401 selectin E P16581
C0007786 Brain Ischemia SELE 6401 selectin E P16581
C0343641 Human papilloma virus infection SELE 6401 selectin E P16581
C0004096 Asthma SELE 6401 selectin E P16581
C0040028 Thrombocythemia, Essential SELE 6401 selectin E P16581
C4082937 Necrotizing enterocolitis in fetus OR newborn SELE 6401 selectin E P16581
C0014070 Encephalomyelitis SELE 6401 selectin E P16581
C0036202 Sarcoidosis SELE 6401 selectin E P16581
C0086981 Sicca Syndrome SELE 6401 selectin E P16581
C4552000 Episodic Kinesigenic Dyskinesia 1 SELE 6401 selectin E P16581

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Last updated: August 19, 2024