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 50876 - 50900 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name ▲ UniProt ID
C0442874 Neuropathy PRNP 5621 prion protein F7VJQ1
C0027819 Neuroblastoma PRNP 5621 prion protein F7VJQ1
C4281802 Spongiform encephalopathy PRNP 5621 prion protein F7VJQ1
C0085584 Encephalopathies PRNP 5621 prion protein F7VJQ1
C0700095 Central neuroblastoma PRNP 5621 prion protein F7VJQ1
C0751781 Dentatorubral-Pallidoluysian Atrophy PRNP 5621 prion protein F7VJQ1
C1621958 Glioblastoma Multiforme PRNP 5621 prion protein F7VJQ1
C1335302 Pancreatic Ductal Adenocarcinoma PRNP 5621 prion protein F7VJQ1
C0004114 Astrocytoma PRNP 5621 prion protein F7VJQ1
C0011265 Presenile dementia PRNP 5621 prion protein F7VJQ1
C0270911 Charcot-Marie-Tooth Disease, Type Ia (disorder) PRNP 5621 prion protein F7VJQ1
C0346647 Malignant neoplasm of pancreas PRNP 5621 prion protein F7VJQ1
C1319315 Adenocarcinoma of large intestine PRNP 5621 prion protein F7VJQ1
C0276496 Familial Alzheimer Disease (FAD) PRNP 5621 prion protein F7VJQ1
C0751254 Creutzfeldt-Jakob Disease, Familial PRNP 5621 prion protein F7VJQ1
C0340978 May-Hegglin anomaly PRNP 5621 prion protein F7VJQ1
C1135993 Wasting Disease, Chronic PRNP 5621 prion protein F7VJQ1
C0023524 Leukoencephalopathy, Progressive Multifocal PRNP 5621 prion protein F7VJQ1
C0015934 Fetal Growth Retardation PRNP 5621 prion protein F7VJQ1
C0000768 Congenital Abnormality PRNP 5621 prion protein F7VJQ1
C0017636 Glioblastoma PRNP 5621 prion protein F7VJQ1
C0041696 Unipolar Depression PRNP 5621 prion protein F7VJQ1
C1306459 Primary malignant neoplasm PRNP 5621 prion protein F7VJQ1
C0339573 Glaucoma, Primary Open Angle PRNP 5621 prion protein F7VJQ1
C0006826 Malignant Neoplasms PRNP 5621 prion protein F7VJQ1

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Last updated: August 19, 2024