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 53476 - 53500 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▼
C0349081 Dementia in Parkinson's disease PRNP 5621 prion protein P04156
C0036457 Scrapie PRNP 5621 prion protein P04156
C1568272 Tendinopathy PRNP 5621 prion protein P04156
C0282513 Primary Progressive Aphasia (disorder) PRNP 5621 prion protein P04156
C0014038 Encephalitis PRNP 5621 prion protein P04156
C1263846 Attention deficit hyperactivity disorder PRNP 5621 prion protein P04156
C0027066 Myoclonus PRNP 5621 prion protein P04156
C0409959 Osteoarthritis, Knee PRNP 5621 prion protein P04156
C0752125 Spinocerebellar Ataxia Type 7 PRNP 5621 prion protein P04156
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

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Last updated: August 19, 2024