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 53401 - 53425 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▼
C0026650 Movement Disorders PRNP 5621 prion protein P04156
C0206042 Fatal Familial Insomnia PRNP 5621 prion protein P04156
C0022336 Creutzfeldt-Jakob disease PRNP 5621 prion protein P04156
C0002726 Amyloidosis PRNP 5621 prion protein P04156
C0027888 Hereditary Motor and Sensory Neuropathies PRNP 5621 prion protein P04156
C1864112 HUNTINGTON DISEASE-LIKE 1 PRNP 5621 prion protein P04156
C0376329 New Variant Creutzfeldt-Jakob Disease PRNP 5621 prion protein P04156
C0007758 Cerebellar Ataxia PRNP 5621 prion protein P04156
C0376358 Malignant neoplasm of prostate PRNP 5621 prion protein P04156
C0022802 Kuru PRNP 5621 prion protein P04156
C1561643 Chronic Kidney Diseases PRNP 5621 prion protein P04156
C0343641 Human papilloma virus infection PRNP 5621 prion protein P04156
C0009402 Colorectal Carcinoma PRNP 5621 prion protein P04156
C0027651 Neoplasms PRNP 5621 prion protein P04156
C0497327 Dementia PRNP 5621 prion protein P04156
C0442874 Neuropathy PRNP 5621 prion protein P04156
C0027819 Neuroblastoma PRNP 5621 prion protein P04156
C4281802 Spongiform encephalopathy PRNP 5621 prion protein P04156
C0085584 Encephalopathies PRNP 5621 prion protein P04156
C0700095 Central neuroblastoma PRNP 5621 prion protein P04156
C0751781 Dentatorubral-Pallidoluysian Atrophy PRNP 5621 prion protein P04156
C1621958 Glioblastoma Multiforme PRNP 5621 prion protein P04156
C1335302 Pancreatic Ductal Adenocarcinoma PRNP 5621 prion protein P04156
C0004114 Astrocytoma PRNP 5621 prion protein P04156
C0011265 Presenile dementia PRNP 5621 prion protein P04156

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Last updated: August 19, 2024