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 50951 - 50975 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name ▲ UniProt ID
C0024790 Paroxysmal nocturnal hemoglobinuria PRNP 5621 prion protein F7VJQ1
C0026848 Myopathy PRNP 5621 prion protein F7VJQ1
C3665347 Visual Impairment PRNP 5621 prion protein F7VJQ1
C0393547 Bulbospinal Neuronopathy PRNP 5621 prion protein F7VJQ1
C0036572 Seizures PRNP 5621 prion protein F7VJQ1
C0011884 Diabetic Retinopathy PRNP 5621 prion protein F7VJQ1
C0040997 Trigeminal Neuralgia PRNP 5621 prion protein F7VJQ1
C0028841 Ocular Hypotension PRNP 5621 prion protein F7VJQ1
C3495559 Juvenile arthritis PRNP 5621 prion protein F7VJQ1
C0021400 Influenza PRNP 5621 prion protein F7VJQ1
C0007760 Cerebellar Diseases PRNP 5621 prion protein F7VJQ1
C0393911 Pure Autonomic Failure PRNP 5621 prion protein F7VJQ1
C0235974 Pancreatic carcinoma PRNP 5621 prion protein F7VJQ1
C0031117 Peripheral Neuropathy PRNP 5621 prion protein F7VJQ1
C0027126 Myotonic Dystrophy PRNP 5621 prion protein F7VJQ1
C0751785 Unverricht-Lundborg Syndrome PRNP 5621 prion protein F7VJQ1
C0025202 melanoma PRNP 5621 prion protein F7VJQ1
C0263912 Rotator cuff syndrome PRNP 5621 prion protein F7VJQ1
C0011269 Dementia, Vascular PRNP 5621 prion protein F7VJQ1
C0677886 Epithelial ovarian cancer PRNP 5621 prion protein F7VJQ1
C0033578 Prostatic Neoplasms PRNP 5621 prion protein F7VJQ1
C0033975 Psychotic Disorders PRNP 5621 prion protein F7VJQ1
C1839259 Bulbo-Spinal Atrophy, X-Linked PRNP 5621 prion protein F7VJQ1
C2750737 DIARRHEA 5, WITH TUFTING ENTEROPATHY, CONGENITAL PRNP 5621 prion protein F7VJQ1
C0038356 Stomach Neoplasms PRNP 5621 prion protein F7VJQ1

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Last updated: August 19, 2024