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 251 - 275 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name ▼ UniProt ID
C0017668 Focal glomerulosclerosis VCAN 1462 versican P13611
C0235974 Pancreatic carcinoma VCAN 1462 versican P13611
C0009402 Colorectal Carcinoma VCAN 1462 versican P13611
C0042164 Uveitis VCAN 1462 versican P13611
C0862312 Epithelioid mesothelioma, malignant VCAN 1462 versican P13611
C0029463 Osteosarcoma VCAN 1462 versican P13611
C0008479 Chondrosarcoma VCAN 1462 versican P13611
C0085786 Hamman-Rich syndrome VCAN 1462 versican P13611
C2350236 Idiopathic Interstitial Pneumonias VCAN 1462 versican P13611
C0019163 Hepatitis B VCAN 1462 versican P13611
C0007222 Cardiovascular Diseases VCAN 1462 versican P13611
C0206647 Dermatofibrosarcoma VCAN 1462 versican P13611
C0002395 Alzheimer's Disease VCAN 1462 versican P13611
C0684249 Carcinoma of lung VCAN 1462 versican P13611
C0037286 Skin Neoplasms VCAN 1462 versican P13611
C0699885 Carcinoma of bladder VCAN 1462 versican P13611
C1314694 Astrocytoma, low grade VCAN 1462 versican P13611
C0008497 Choriocarcinoma VCAN 1462 versican P13611
C0017601 Glaucoma VCAN 1462 versican P13611
C0007112 Adenocarcinoma of prostate VCAN 1462 versican P13611
C3665347 Visual Impairment VCAN 1462 versican P13611
C3714636 Pneumonitis VCAN 1462 versican P13611
C0238198 Gastrointestinal Stromal Tumors VCAN 1462 versican P13611
C0013264 Muscular Dystrophy, Duchenne VCAN 1462 versican P13611
C4707243 Familial thoracic aortic aneurysm and aortic dissection VCAN 1462 versican P13611

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Last updated: August 19, 2024