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 13201 - 13225 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Gene Name UniProt ID
C0678222 Breast Carcinoma SELP 6403 selectin P P16109
C2239176 Liver carcinoma SELP 6403 selectin P P16109
C0005283 beta Thalassemia SELP 6403 selectin P P16109
C0038013 Ankylosing spondylitis SELP 6403 selectin P P16109
C1704436 Peripheral Arterial Diseases SELP 6403 selectin P P16109
C0007785 Cerebral Infarction SELP 6403 selectin P P16109
C0033860 Psoriasis SELP 6403 selectin P P16109
C0577631 Carotid Atherosclerosis SELP 6403 selectin P P16109
C0011581 Depressive disorder SELP 6403 selectin P P16109
C0006826 Malignant Neoplasms SELP 6403 selectin P P16109
C0684249 Carcinoma of lung SELP 6403 selectin P P16109
C1565489 Renal Insufficiency SELP 6403 selectin P P16109
C0004096 Asthma SELP 6403 selectin P P16109
C0011573 Endogenous depression SELP 6403 selectin P P16109
C0272286 Thrombocytopenia due to platelet alloimmunization SELP 6403 selectin P P16109
C0085261 Proteus Syndrome SELP 6403 selectin P P16109
C0345904 Malignant neoplasm of liver SELP 6403 selectin P P16109
C0242383 Age related macular degeneration SELP 6403 selectin P P16109
C0026691 Mucocutaneous Lymph Node Syndrome SELP 6403 selectin P P16109
C0235974 Pancreatic carcinoma SELP 6403 selectin P P16109
C0524702 Pulmonary Thromboembolisms SELP 6403 selectin P P16109
C0019158 Hepatitis SELP 6403 selectin P P16109
C0152021 Congenital heart disease SELP 6403 selectin P P16109
C2931689 Dystrophia myotonica 2 SELP 6403 selectin P P16109
C0751956 Acute Cerebrovascular Accidents SELP 6403 selectin P P16109

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Last updated: August 19, 2024