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 11726 - 11750 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▲
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
C0033847 Pseudoxanthoma Elasticum GLA 2717 galactosidase alpha P06280
C0022680 Polycystic Kidney Diseases GLA 2717 galactosidase alpha P06280
C0018784 Sensorineural Hearing Loss (disorder) GLA 2717 galactosidase alpha P06280
C0042571 Vertigo GLA 2717 galactosidase alpha P06280
C0024236 Lymphedema GLA 2717 galactosidase alpha P06280
C0020620 Hypohidrosis GLA 2717 galactosidase alpha P06280
C0870082 Hyperkeratosis GLA 2717 galactosidase alpha P06280
C0024115 Lung diseases GLA 2717 galactosidase alpha P06280
C0016034 Breast Fibrocystic Disease GLA 2717 galactosidase alpha P06280
C0011848 Diabetes Insipidus GLA 2717 galactosidase alpha P06280
C0020459 Hyperinsulinism GLA 2717 galactosidase alpha P06280
C0042267 Vaginitis GLA 2717 galactosidase alpha P06280
C0342751 Generalized glycogen storage disease of infants GLA 2717 galactosidase alpha P06280
C4721453 Peripheral Nervous System Diseases GLA 2717 galactosidase alpha P06280
C0231528 Myalgia GLA 2717 galactosidase alpha P06280

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Last updated: August 19, 2024