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 44376 - 44400 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Gene Name UniProt ID
C0007097 Carcinoma PRNP 5621 prion protein F7VJQ1
C0007682 CNS disorder PRNP 5621 prion protein F7VJQ1
C0042900 Vitiligo PRNP 5621 prion protein F7VJQ1
C0020538 Hypertensive disease PRNP 5621 prion protein F7VJQ1
C0917799 Hypersomnia PRNP 5621 prion protein F7VJQ1
C0020456 Hyperglycemia PRNP 5621 prion protein F7VJQ1
C0242379 Malignant neoplasm of lung PRNP 5621 prion protein F7VJQ1
C0007137 Squamous cell carcinoma PRNP 5621 prion protein F7VJQ1
C0268398 Familial lichen amyloidosis PRNP 5621 prion protein F7VJQ1
C0042769 Virus Diseases PRNP 5621 prion protein F7VJQ1
C1835614 Hereditary Hyperexplexia PRNP 5621 prion protein F7VJQ1
C0520966 Abnormal coordination PRNP 5621 prion protein F7VJQ1
C4721610 Carcinoma, Ovarian Epithelial PRNP 5621 prion protein F7VJQ1
C0751777 Familial Progressive Myoclonic Epilepsy PRNP 5621 prion protein F7VJQ1
C0004138 Ataxias, Hereditary PRNP 5621 prion protein F7VJQ1
C0024117 Chronic Obstructive Airway Disease PRNP 5621 prion protein F7VJQ1
C0032002 Pituitary Diseases PRNP 5621 prion protein F7VJQ1
C0003850 Arteriosclerosis PRNP 5621 prion protein F7VJQ1
C0149931 Migraine Disorders PRNP 5621 prion protein F7VJQ1
C1861736 SPINOCEREBELLAR ATAXIA 31 (disorder) PRNP 5621 prion protein F7VJQ1
C0031069 Familial Mediterranean Fever PRNP 5621 prion protein F7VJQ1
C0205710 Alpers Syndrome (disorder) PRNP 5621 prion protein F7VJQ1
C1306600 Radial nerve palsy PRNP 5621 prion protein F7VJQ1
C1708349 Hereditary Diffuse Gastric Cancer PRNP 5621 prion protein F7VJQ1
C1854520 SEBASTIAN SYNDROME PRNP 5621 prion protein F7VJQ1

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Last updated: August 19, 2024