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 9276 - 9300 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▲
C0751779 Action Myoclonus-Renal Failure Syndrome PRNP 5621 prion protein P04156
C0020258 Hydrocephalus, Normal Pressure PRNP 5621 prion protein P04156
C0011311 Dengue Fever PRNP 5621 prion protein P04156
C0270922 Peripheral demyelinating neuropathy PRNP 5621 prion protein P04156
C0010674 Cystic Fibrosis PRNP 5621 prion protein P04156
C0019069 Hemophilia A PRNP 5621 prion protein P04156
C1857276 Trichohepatoenteric Syndrome PRNP 5621 prion protein P04156
C0751645 Human Transmissible Spongiform Encephalopathies, Inherited PRNP 5621 prion protein P04156
C0011991 Diarrhea PRNP 5621 prion protein P04156
C0007786 Brain Ischemia PRNP 5621 prion protein P04156
C0029408 Degenerative polyarthritis PRNP 5621 prion protein P04156
C0233844 Clumsiness PRNP 5621 prion protein P04156
C4721453 Peripheral Nervous System Diseases PRNP 5621 prion protein P04156
C0525045 Mood Disorders PRNP 5621 prion protein P04156
C0751956 Acute Cerebrovascular Accidents PRNP 5621 prion protein P04156
C0008489 Chorea PRNP 5621 prion protein P04156
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

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Last updated: August 19, 2024