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 9226 - 9250 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▲
C0005129 Bernard-Soulier Syndrome PRNP 5621 prion protein P04156
C0036341 Schizophrenia PRNP 5621 prion protein P04156
C0030567 Parkinson Disease PRNP 5621 prion protein P04156
C0949664 Tauopathies PRNP 5621 prion protein P04156
C0752347 Lewy Body Disease PRNP 5621 prion protein P04156
C0014556 Epilepsy, Temporal Lobe PRNP 5621 prion protein P04156
C0024790 Paroxysmal nocturnal hemoglobinuria PRNP 5621 prion protein P04156
C0026848 Myopathy PRNP 5621 prion protein P04156
C3665347 Visual Impairment PRNP 5621 prion protein P04156
C0393547 Bulbospinal Neuronopathy PRNP 5621 prion protein P04156
C0036572 Seizures PRNP 5621 prion protein P04156
C0011884 Diabetic Retinopathy PRNP 5621 prion protein P04156
C0040997 Trigeminal Neuralgia PRNP 5621 prion protein P04156
C0028841 Ocular Hypotension PRNP 5621 prion protein P04156
C3495559 Juvenile arthritis PRNP 5621 prion protein P04156
C0021400 Influenza PRNP 5621 prion protein P04156
C0007760 Cerebellar Diseases PRNP 5621 prion protein P04156
C0393911 Pure Autonomic Failure PRNP 5621 prion protein P04156
C0235974 Pancreatic carcinoma PRNP 5621 prion protein P04156
C0031117 Peripheral Neuropathy PRNP 5621 prion protein P04156
C0027126 Myotonic Dystrophy PRNP 5621 prion protein P04156
C0751785 Unverricht-Lundborg Syndrome PRNP 5621 prion protein P04156
C0025202 melanoma PRNP 5621 prion protein P04156
C0263912 Rotator cuff syndrome PRNP 5621 prion protein P04156
C0011269 Dementia, Vascular PRNP 5621 prion protein P04156

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Last updated: August 19, 2024