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 51001 - 51025 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name ▲ UniProt ID
C1857276 Trichohepatoenteric Syndrome PRNP 5621 prion protein F7VJQ1
C0751645 Human Transmissible Spongiform Encephalopathies, Inherited PRNP 5621 prion protein F7VJQ1
C0011991 Diarrhea PRNP 5621 prion protein F7VJQ1
C0007786 Brain Ischemia PRNP 5621 prion protein F7VJQ1
C0029408 Degenerative polyarthritis PRNP 5621 prion protein F7VJQ1
C0233844 Clumsiness PRNP 5621 prion protein F7VJQ1
C4721453 Peripheral Nervous System Diseases PRNP 5621 prion protein F7VJQ1
C0525045 Mood Disorders PRNP 5621 prion protein F7VJQ1
C0751956 Acute Cerebrovascular Accidents PRNP 5621 prion protein F7VJQ1
C0008489 Chorea PRNP 5621 prion protein F7VJQ1
C0684249 Carcinoma of lung PRNP 5621 prion protein F7VJQ1
C0001175 Acquired Immunodeficiency Syndrome PRNP 5621 prion protein F7VJQ1
C0017638 Glioma PRNP 5621 prion protein F7VJQ1
C0038868 Progressive supranuclear palsy PRNP 5621 prion protein F7VJQ1
C0751494 Convulsive Seizures PRNP 5621 prion protein F7VJQ1
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

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Last updated: August 19, 2024