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 12051 - 12075 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name ▼ UniProt ID
C0751713 Inclusion Body Myopathy, Sporadic PRNP 5621 prion protein F7VJQ1
C0007785 Cerebral Infarction PRNP 5621 prion protein F7VJQ1
C0259749 Autonomic neuropathy PRNP 5621 prion protein F7VJQ1
C0029463 Osteosarcoma PRNP 5621 prion protein F7VJQ1
C0032897 Prader-Willi Syndrome PRNP 5621 prion protein F7VJQ1
C0035334 Retinitis Pigmentosa PRNP 5621 prion protein F7VJQ1
C1168401 Squamous cell carcinoma of the head and neck PRNP 5621 prion protein F7VJQ1
C0005586 Bipolar Disorder PRNP 5621 prion protein F7VJQ1
C0007134 Renal Cell Carcinoma PRNP 5621 prion protein F7VJQ1
C1378703 Renal carcinoma PRNP 5621 prion protein F7VJQ1
C0027809 Neurilemmoma PRNP 5621 prion protein F7VJQ1
C0751782 May-White Syndrome PRNP 5621 prion protein F7VJQ1
C0751780 Biotin-Responsive Encephalopathy PRNP 5621 prion protein F7VJQ1
C1531647 Cerebral ventriculomegaly PRNP 5621 prion protein F7VJQ1
C0007097 Carcinoma PRNP 5621 prion protein F7VJQ1
C0007682 CNS disorder PRNP 5621 prion protein F7VJQ1
C0042900 Vitiligo PRNP 5621 prion protein F7VJQ1
C0020538 Hypertensive disease PRNP 5621 prion protein F7VJQ1
C0917799 Hypersomnia PRNP 5621 prion protein F7VJQ1
C0020456 Hyperglycemia PRNP 5621 prion protein F7VJQ1
C0242379 Malignant neoplasm of lung PRNP 5621 prion protein F7VJQ1
C0007137 Squamous cell carcinoma PRNP 5621 prion protein F7VJQ1
C0268398 Familial lichen amyloidosis PRNP 5621 prion protein F7VJQ1
C0042769 Virus Diseases PRNP 5621 prion protein F7VJQ1
C1835614 Hereditary Hyperexplexia PRNP 5621 prion protein F7VJQ1

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Last updated: August 19, 2024