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 50976 - 51000 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name ▲ UniProt ID
C3805618 CEREBRAL AMYLOID ANGIOPATHY, PRNP-RELATED PRNP 5621 prion protein F7VJQ1
C0233794 Memory impairment PRNP 5621 prion protein F7VJQ1
C0006111 Brain Diseases PRNP 5621 prion protein F7VJQ1
C0025289 Meningitis PRNP 5621 prion protein F7VJQ1
C0009946 Conversion disorder PRNP 5621 prion protein F7VJQ1
C0242422 Parkinsonian Disorders PRNP 5621 prion protein F7VJQ1
C0278878 Adult Glioblastoma PRNP 5621 prion protein F7VJQ1
C1269683 Major Depressive Disorder PRNP 5621 prion protein F7VJQ1
C0004096 Asthma PRNP 5621 prion protein F7VJQ1
C1458155 Mammary Neoplasms PRNP 5621 prion protein F7VJQ1
C2239176 Liver carcinoma PRNP 5621 prion protein F7VJQ1
C0004153 Atherosclerosis PRNP 5621 prion protein F7VJQ1
C0003467 Anxiety PRNP 5621 prion protein F7VJQ1
C0751778 Myoclonic Epilepsies, Progressive PRNP 5621 prion protein F7VJQ1
C0019187 Hepatitis, Alcoholic PRNP 5621 prion protein F7VJQ1
C0155379 Nystagmus associated with disorder of the vestibular system PRNP 5621 prion protein F7VJQ1
C0751776 Atypical Inclusion-Body Disease PRNP 5621 prion protein F7VJQ1
C0011581 Depressive disorder PRNP 5621 prion protein F7VJQ1
C1285162 Degenerative disorder PRNP 5621 prion protein F7VJQ1
C0751779 Action Myoclonus-Renal Failure Syndrome PRNP 5621 prion protein F7VJQ1
C0020258 Hydrocephalus, Normal Pressure PRNP 5621 prion protein F7VJQ1
C0011311 Dengue Fever PRNP 5621 prion protein F7VJQ1
C0270922 Peripheral demyelinating neuropathy PRNP 5621 prion protein F7VJQ1
C0010674 Cystic Fibrosis PRNP 5621 prion protein F7VJQ1
C0019069 Hemophilia A PRNP 5621 prion protein F7VJQ1

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Last updated: August 19, 2024