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 49376 - 49400 of 62743 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Gene Name UniProt ID
C0003537 Aphasia PRNP 5621 prion protein P04156
C0024623 Malignant neoplasm of stomach PRNP 5621 prion protein P04156
C0009404 Colorectal Neoplasms PRNP 5621 prion protein P04156
C1832661 ANOPHTHALMIA AND PULMONARY HYPOPLASIA PRNP 5621 prion protein P04156
C0014544 Epilepsy PRNP 5621 prion protein P04156
C0338451 Frontotemporal dementia PRNP 5621 prion protein P04156
C1853926 NONAKA MYOPATHY PRNP 5621 prion protein P04156
C0032027 Pityriasis Rubra Pilaris PRNP 5621 prion protein P04156
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

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Last updated: August 19, 2024