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 11926 - 11950 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name ▼ UniProt ID
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
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

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Last updated: August 19, 2024