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 39176 - 39200 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name ▲ UniProt ID
C0033375 Prolactinoma MGAM 8972 maltase-glucoamylase O43451
C0007222 Cardiovascular Diseases MGAM 8972 maltase-glucoamylase O43451
C0678222 Breast Carcinoma MGAM 8972 maltase-glucoamylase O43451
C0282577 Congenital Disorders of Glycosylation MGAM 8972 maltase-glucoamylase O43451
C0009806 Constipation MGAM 8972 maltase-glucoamylase O43451
C0042769 Virus Diseases MGAM 8972 maltase-glucoamylase O43451
C0026848 Myopathy MGAM 8972 maltase-glucoamylase O43451
C0027651 Neoplasms MGAM 8972 maltase-glucoamylase O43451
C0545044 Acrokeratoelastoidosis of Costa MGAM 8972 maltase-glucoamylase O43451
C0011860 Diabetes Mellitus, Non-Insulin-Dependent MGAM 8972 maltase-glucoamylase O43451
C1862103 Brachydactyly type C MGAM 8972 maltase-glucoamylase O43451
C4551472 Hypertrophic obstructive cardiomyopathy MGAM 8972 maltase-glucoamylase O43451
C0010068 Coronary heart disease MGAM 8972 maltase-glucoamylase O43451
C0011849 Diabetes Mellitus MGAM 8972 maltase-glucoamylase O43451
C0011311 Dengue Fever MGAM 8972 maltase-glucoamylase O43451
C0027868 Neuromuscular Diseases MGAM 8972 maltase-glucoamylase O43451
C0007137 Squamous cell carcinoma MGAM 8972 maltase-glucoamylase O43451
C0002736 Amyotrophic Lateral Sclerosis MGAM 8972 maltase-glucoamylase O43451
C0017921 Glycogen storage disease type II MGAM 8972 maltase-glucoamylase O43451
C1449563 Cardiomyopathy, Familial Idiopathic MGAM 8972 maltase-glucoamylase O43451
C1956346 Coronary Artery Disease MGAM 8972 maltase-glucoamylase O43451
C0017495 Gerstmann-Straussler-Scheinker Disease MGAM 8972 maltase-glucoamylase O43451
C0007194 Hypertrophic Cardiomyopathy MGAM 8972 maltase-glucoamylase O43451
C1833662 INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE AND FRONTOTEMPORAL DEMENTIA MASP1 5648 mannan binding lectin serine peptidase 1 P48740
C0008924 Cleft upper lip MASP1 5648 mannan binding lectin serine peptidase 1 P48740

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Last updated: August 19, 2024