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 9201 - 9225 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▲
C0013080 Down Syndrome PRNP 5621 prion protein P04156
C0001418 Adenocarcinoma PRNP 5621 prion protein P04156
C0494463 Alzheimer Disease, Late Onset PRNP 5621 prion protein P04156
C0087012 Ataxia, Spinocerebellar PRNP 5621 prion protein P04156
C0750901 Alzheimer Disease, Early Onset PRNP 5621 prion protein P04156
C0152013 Adenocarcinoma of lung (disorder) PRNP 5621 prion protein P04156
C0008479 Chondrosarcoma PRNP 5621 prion protein P04156
C1867773 CEREBRAL AMYLOID ANGIOPATHY, ITM2B-RELATED, 1 PRNP 5621 prion protein P04156
C0020179 Huntington Disease PRNP 5621 prion protein P04156
C0019202 Hepatolenticular Degeneration PRNP 5621 prion protein P04156
C0019196 Hepatitis C PRNP 5621 prion protein P04156
C0027765 nervous system disorder PRNP 5621 prion protein P04156
C0019163 Hepatitis B PRNP 5621 prion protein P04156
C0002736 Amyotrophic Lateral Sclerosis PRNP 5621 prion protein P04156
C0585442 Osteosarcoma of bone PRNP 5621 prion protein P04156
C2931022 Amyloidosis, Cerebral, with Spongiform Encephalopathy PRNP 5621 prion protein P04156
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

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Last updated: August 19, 2024