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 62326 - 62350 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▼
C0003635 Apraxias PRNP 5621 prion protein F7VJQ1
C0038644 Sudden infant death syndrome PRNP 5621 prion protein F7VJQ1
C0021390 Inflammatory Bowel Diseases PRNP 5621 prion protein F7VJQ1
C0028754 Obesity PRNP 5621 prion protein F7VJQ1
C0152025 Polyneuropathy PRNP 5621 prion protein F7VJQ1
C0699791 Stomach Carcinoma PRNP 5621 prion protein F7VJQ1
C0026769 Multiple Sclerosis PRNP 5621 prion protein F7VJQ1
C0678222 Breast Carcinoma PRNP 5621 prion protein F7VJQ1
C0162635 Angelman Syndrome PRNP 5621 prion protein F7VJQ1
C0236642 Pick Disease of the Brain PRNP 5621 prion protein F7VJQ1
C0039103 Synovitis PRNP 5621 prion protein F7VJQ1
C0003537 Aphasia PRNP 5621 prion protein F7VJQ1
C0024623 Malignant neoplasm of stomach PRNP 5621 prion protein F7VJQ1
C0009404 Colorectal Neoplasms PRNP 5621 prion protein F7VJQ1
C1832661 ANOPHTHALMIA AND PULMONARY HYPOPLASIA PRNP 5621 prion protein F7VJQ1
C0014544 Epilepsy PRNP 5621 prion protein F7VJQ1
C0338451 Frontotemporal dementia PRNP 5621 prion protein F7VJQ1
C1853926 NONAKA MYOPATHY PRNP 5621 prion protein F7VJQ1
C0032027 Pityriasis Rubra Pilaris PRNP 5621 prion protein F7VJQ1
C0013080 Down Syndrome PRNP 5621 prion protein F7VJQ1
C0001418 Adenocarcinoma PRNP 5621 prion protein F7VJQ1
C0494463 Alzheimer Disease, Late Onset PRNP 5621 prion protein F7VJQ1
C0087012 Ataxia, Spinocerebellar PRNP 5621 prion protein F7VJQ1
C0750901 Alzheimer Disease, Early Onset PRNP 5621 prion protein F7VJQ1
C0152013 Adenocarcinoma of lung (disorder) PRNP 5621 prion protein F7VJQ1

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Last updated: August 19, 2024