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 14626 - 14650 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name ▼ UniProt ID
C0011849 Diabetes Mellitus PLA2G7 7941 phospholipase A2 group VII Q13093
C0745103 Hyperlipoproteinemia Type IIa PLA2G7 7941 phospholipase A2 group VII Q13093
C0027726 Nephrotic Syndrome PLA2G7 7941 phospholipase A2 group VII Q13093
C0007193 Cardiomyopathy, Dilated PLA2G7 7941 phospholipase A2 group VII Q13093
C0002726 Amyloidosis PLA2G7 7941 phospholipase A2 group VII Q13093
C0400966 Non-alcoholic Fatty Liver Disease PLA2G7 7941 phospholipase A2 group VII Q13093
C0032580 Adenomatous Polyposis Coli PLA2G7 7941 phospholipase A2 group VII Q13093
C0028754 Obesity PLA2G7 7941 phospholipase A2 group VII Q13093
C0020597 Hypobetalipoproteinemias PLA2G7 7941 phospholipase A2 group VII Q13093
C0497327 Dementia PLA2G7 7941 phospholipase A2 group VII Q13093
C0004606 Nonproliferative diabetic retinopathy PLA2G7 7941 phospholipase A2 group VII Q13093
C0011860 Diabetes Mellitus, Non-Insulin-Dependent PLA2G7 7941 phospholipase A2 group VII Q13093
C0001339 Acute pancreatitis PLA2G7 7941 phospholipase A2 group VII Q13093
C0020542 Pulmonary Hypertension PLA2G7 7941 phospholipase A2 group VII Q13093
C0740394 Hyperuricemia PLA2G7 7941 phospholipase A2 group VII Q13093
C0025521 Inborn Errors of Metabolism PLA2G7 7941 phospholipase A2 group VII Q13093
C0009324 Ulcerative Colitis PLA2G7 7941 phospholipase A2 group VII Q13093
C1862596 Familial hypobetalipoproteinemia PLA2G7 7941 phospholipase A2 group VII Q13093
C0004238 Atrial Fibrillation PLA2G7 7941 phospholipase A2 group VII Q13093
C0494463 Alzheimer Disease, Late Onset PLA2G7 7941 phospholipase A2 group VII Q13093
C0007194 Hypertrophic Cardiomyopathy PLA2G7 7941 phospholipase A2 group VII Q13093
C0699790 Colon Carcinoma PLA2G7 7941 phospholipase A2 group VII Q13093
C1449563 Cardiomyopathy, Familial Idiopathic PLA2G7 7941 phospholipase A2 group VII Q13093
C2607914 Allergic rhinitis (disorder) PLA2G7 7941 phospholipase A2 group VII Q13093
C0220668 Congenital contractural arachnodactyly PLA2G7 7941 phospholipase A2 group VII Q13093

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Last updated: August 19, 2024