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 11751 - 11775 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Gene Name UniProt ID
C0003864 Arthritis AGA 175 aspartylglucosaminidase P20933
C0019270 Hernia AGA 175 aspartylglucosaminidase P20933
C0041296 Tuberculosis AGA 175 aspartylglucosaminidase P20933
C0014038 Encephalitis AGA 175 aspartylglucosaminidase P20933
C0702166 Acne AGA 175 aspartylglucosaminidase P20933
C0019187 Hepatitis, Alcoholic AGA 175 aspartylglucosaminidase P20933
C0026266 Mitral Valve Insufficiency AGA 175 aspartylglucosaminidase P20933
C0086543 Cataract AGA 175 aspartylglucosaminidase P20933
C0013384 Dyskinetic syndrome AGA 175 aspartylglucosaminidase P20933
C0221356 Brachycephaly AGA 175 aspartylglucosaminidase P20933
C0086795 Pfaundler-Hurler Syndrome AGA 175 aspartylglucosaminidase P20933
C0024143 Lupus Nephritis AGA 175 aspartylglucosaminidase P20933
C0014852 Esophageal Diseases AGA 175 aspartylglucosaminidase P20933
C0037822 Speech Disorders AGA 175 aspartylglucosaminidase P20933
C0566602 Primary sclerosing cholangitis AGA 175 aspartylglucosaminidase P20933
C0011854 Diabetes Mellitus, Insulin-Dependent AGA 175 aspartylglucosaminidase P20933
C3714756 Intellectual Disability AGA 175 aspartylglucosaminidase P20933
C0036337 Schizoaffective Disorder AGA 175 aspartylglucosaminidase P20933
C0025958 Microcephaly AGA 175 aspartylglucosaminidase P20933
C0341106 Eosinophilic esophagitis AGA 175 aspartylglucosaminidase P20933
C0036572 Seizures AGA 175 aspartylglucosaminidase P20933
C0162323 Polyarthritis ACAN 176 aggrecan P16112
C0013336 Dwarfism ACAN 176 aggrecan P16112
C0003864 Arthritis ACAN 176 aggrecan P16112
C0595989 Carcinoma of larynx ACAN 176 aggrecan P16112

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Last updated: August 19, 2024