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 50976 - 51000 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Gene Name UniProt ID
C0268225 Aspartylglucosaminuria AGA 175 aspartylglucosaminidase P20933
C0019196 Hepatitis C AGA 175 aspartylglucosaminidase P20933
C0162311 Androgenetic Alopecia AGA 175 aspartylglucosaminidase P20933
C0699791 Stomach Carcinoma AGA 175 aspartylglucosaminidase P20933
C0008325 Cholecystitis AGA 175 aspartylglucosaminidase P20933
C0085207 Gestational Diabetes AGA 175 aspartylglucosaminidase P20933
C0022104 Irritable Bowel Syndrome AGA 175 aspartylglucosaminidase P20933
C0036341 Schizophrenia AGA 175 aspartylglucosaminidase P20933
C0524620 Metabolic Syndrome X AGA 175 aspartylglucosaminidase P20933
C0019294 Hernia, Inguinal AGA 175 aspartylglucosaminidase P20933
C0011847 Diabetes AGA 175 aspartylglucosaminidase P20933
C0007570 Celiac Disease AGA 175 aspartylglucosaminidase P20933
C0038018 Spondylolysis AGA 175 aspartylglucosaminidase P20933
C0016202 Flatfoot AGA 175 aspartylglucosaminidase P20933
C0040128 Thyroid Diseases AGA 175 aspartylglucosaminidase P20933
C0235946 Cerebral atrophy AGA 175 aspartylglucosaminidase P20933
C2931840 Aspartylglucosamidase (AGA) deficiency AGA 175 aspartylglucosaminidase P20933
C0024623 Malignant neoplasm of stomach AGA 175 aspartylglucosaminidase P20933
C2239176 Liver carcinoma AGA 175 aspartylglucosaminidase P20933
C4083212 Alopecia, Male Pattern AGA 175 aspartylglucosaminidase P20933
C0026769 Multiple Sclerosis AGA 175 aspartylglucosaminidase P20933
C0013336 Dwarfism AGA 175 aspartylglucosaminidase P20933
C0282577 Congenital Disorders of Glycosylation AGA 175 aspartylglucosaminidase P20933
C1321756 Achalasia AGA 175 aspartylglucosaminidase P20933
C0023890 Liver Cirrhosis AGA 175 aspartylglucosaminidase P20933

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Last updated: August 19, 2024