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 53551 - 53575 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▼
C0684249 Carcinoma of lung PRNP 5621 prion protein P04156
C0001175 Acquired Immunodeficiency Syndrome PRNP 5621 prion protein P04156
C0017638 Glioma PRNP 5621 prion protein P04156
C0038868 Progressive supranuclear palsy PRNP 5621 prion protein P04156
C0751494 Convulsive Seizures PRNP 5621 prion protein P04156
C0751713 Inclusion Body Myopathy, Sporadic PRNP 5621 prion protein P04156
C0007785 Cerebral Infarction PRNP 5621 prion protein P04156
C0259749 Autonomic neuropathy PRNP 5621 prion protein P04156
C0029463 Osteosarcoma PRNP 5621 prion protein P04156
C0032897 Prader-Willi Syndrome PRNP 5621 prion protein P04156
C0035334 Retinitis Pigmentosa PRNP 5621 prion protein P04156
C1168401 Squamous cell carcinoma of the head and neck PRNP 5621 prion protein P04156
C0005586 Bipolar Disorder PRNP 5621 prion protein P04156
C0007134 Renal Cell Carcinoma PRNP 5621 prion protein P04156
C1378703 Renal carcinoma PRNP 5621 prion protein P04156
C0027809 Neurilemmoma PRNP 5621 prion protein P04156
C0751782 May-White Syndrome PRNP 5621 prion protein P04156
C0751780 Biotin-Responsive Encephalopathy PRNP 5621 prion protein P04156
C1531647 Cerebral ventriculomegaly PRNP 5621 prion protein P04156
C0007097 Carcinoma PRNP 5621 prion protein P04156
C0007682 CNS disorder PRNP 5621 prion protein P04156
C0042900 Vitiligo PRNP 5621 prion protein P04156
C0020538 Hypertensive disease PRNP 5621 prion protein P04156
C0917799 Hypersomnia PRNP 5621 prion protein P04156
C0020456 Hyperglycemia PRNP 5621 prion protein P04156

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Last updated: August 19, 2024