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 51026 - 51050 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▼
C1561643 Chronic Kidney Diseases GLA 2717 galactosidase alpha P06280
C0011581 Depressive disorder GLA 2717 galactosidase alpha P06280
C0027726 Nephrotic Syndrome GLA 2717 galactosidase alpha P06280
C0010036 Corneal dystrophy GLA 2717 galactosidase alpha P06280
C0017921 Glycogen storage disease type II GLA 2717 galactosidase alpha P06280
C0020615 Hypoglycemia GLA 2717 galactosidase alpha P06280
C0917805 Transient Cerebral Ischemia GLA 2717 galactosidase alpha P06280
C3160718 PARKINSON DISEASE, LATE-ONSET GLA 2717 galactosidase alpha P06280
C0007787 Transient Ischemic Attack GLA 2717 galactosidase alpha P06280
C0029410 Osteoarthritis of hip GLA 2717 galactosidase alpha P06280
C0007820 Cerebrovascular Disorders GLA 2717 galactosidase alpha P06280
C0042880 Vitamin K Deficiency GLA 2717 galactosidase alpha P06280
C0002985 Angiokeratoma GLA 2717 galactosidase alpha P06280
C0004245 Atrioventricular Block GLA 2717 galactosidase alpha P06280
C0006309 Brucellosis GLA 2717 galactosidase alpha P06280
C0029124 Optic Atrophy GLA 2717 galactosidase alpha P06280
C0014805 Primary Erythermalgia GLA 2717 galactosidase alpha P06280
C0242666 Protein S Deficiency GLA 2717 galactosidase alpha P06280
C0013364 Dysautonomia, Familial GLA 2717 galactosidase alpha P06280
C0033687 Proteinuria GLA 2717 galactosidase alpha P06280
C0031069 Familial Mediterranean Fever GLA 2717 galactosidase alpha P06280
C0025521 Inborn Errors of Metabolism GLA 2717 galactosidase alpha P06280
C0021400 Influenza GLA 2717 galactosidase alpha P06280
C0020473 Hyperlipidemia GLA 2717 galactosidase alpha P06280
C0033117 Priapism GLA 2717 galactosidase alpha P06280

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Last updated: August 19, 2024