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 62426 - 62450 of 62743 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Gene Name UniProt ID
C4707243 Familial thoracic aortic aneurysm and aortic dissection VCAN 1462 versican P13611
C0024796 Marfan Syndrome VCAN 1462 versican P13611
C0279000 Liver and Intrahepatic Biliary Tract Carcinoma VCAN 1462 versican P13611
C0555198 Malignant Glioma VCAN 1462 versican P13611
C0282160 Aplasia Cutis Congenita VCAN 1462 versican P13611
C0178664 Glomerulosclerosis (disorder) VCAN 1462 versican P13611
C0027962 Melanocytic nevus VCAN 1462 versican P13611
C0242379 Malignant neoplasm of lung VCAN 1462 versican P13611
C0007107 Malignant neoplasm of larynx VCAN 1462 versican P13611
C0021775 Intermittent Claudication VCAN 1462 versican P13611
C0033860 Psoriasis VNN1 8876 vanin 1 O95497
C0025517 Metabolic Diseases VNN1 8876 vanin 1 O95497
C0015624 Fanconi Syndrome VNN1 8876 vanin 1 O95497
C1306459 Primary malignant neoplasm VNN1 8876 vanin 1 O95497
C0009402 Colorectal Carcinoma VNN1 8876 vanin 1 O95497
C0178664 Glomerulosclerosis (disorder) VNN1 8876 vanin 1 O95497
C0149939 Obstructive nephropathy VNN1 8876 vanin 1 O95497
C0004153 Atherosclerosis VNN1 8876 vanin 1 O95497
C0699790 Colon Carcinoma VNN1 8876 vanin 1 O95497
C0020538 Hypertensive disease VNN1 8876 vanin 1 O95497
C0041956 Ureteral obstruction VNN1 8876 vanin 1 O95497
C0079731 B-Cell Lymphomas VNN1 8876 vanin 1 O95497
C0004096 Asthma VNN1 8876 vanin 1 O95497
C0020295 Hydronephrosis VNN1 8876 vanin 1 O95497
C0030246 Pustulosis of Palms and Soles VNN1 8876 vanin 1 O95497

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Last updated: August 19, 2024