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 41776 - 41800 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Gene Name UniProt ID
C0036572 Seizures GLA 2717 galactosidase alpha P06280
C0032285 Pneumonia GLA 2717 galactosidase alpha P06280
C0042373 Vascular Diseases GLA 2717 galactosidase alpha P06280
C0010038 Corneal Opacity GLA 2717 galactosidase alpha P06280
C0028064 Niemann-Pick Diseases GLA 2717 galactosidase alpha P06280
C0041349 Nephritis, Tubulointerstitial GLA 2717 galactosidase alpha P06280
C0035078 Kidney Failure GLA 2717 galactosidase alpha P06280
C0013336 Dwarfism GLA 2717 galactosidase alpha P06280
C0025517 Metabolic Diseases GLA 2717 galactosidase alpha P06280
C0017601 Glaucoma GLA 2717 galactosidase alpha P06280
C0006142 Malignant neoplasm of breast GLA 2717 galactosidase alpha P06280
C0026654 Moyamoya Disease GLA 2717 galactosidase alpha P06280
C0700345 Candidiasis, Vulvovaginal GLA 2717 galactosidase alpha P06280
C0017919 Glycogen Storage Disease GLA 2717 galactosidase alpha P06280
C0018799 Heart Diseases GLA 2717 galactosidase alpha P06280
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

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Last updated: August 19, 2024