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 60326 - 60350 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▲
C0010417 Cryptorchidism B4GALT7 11285 beta-1,4-galactosyltransferase 7 Q9UBV7
C0009319 Colitis B4GALT7 11285 beta-1,4-galactosyltransferase 7 Q9UBV7
C3278404 MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS B4GALT7 11285 beta-1,4-galactosyltransferase 7 Q9UBV7
C0009207 Cockayne Syndrome B4GALT7 11285 beta-1,4-galactosyltransferase 7 Q9UBV7
C0010495 Cutis Laxa B4GALT7 11285 beta-1,4-galactosyltransferase 7 Q9UBV7
C0158761 Radioulnar Synostosis B4GALT7 11285 beta-1,4-galactosyltransferase 7 Q9UBV7
C0009782 Connective Tissue Diseases B4GALT7 11285 beta-1,4-galactosyltransferase 7 Q9UBV7
C0003507 Aortic Valve Stenosis B4GALT7 11285 beta-1,4-galactosyltransferase 7 Q9UBV7
C0013336 Dwarfism B4GALT7 11285 beta-1,4-galactosyltransferase 7 Q9UBV7
C0037856 Spermatic Cord Torsion B4GALT7 11285 beta-1,4-galactosyltransferase 7 Q9UBV7
C0017574 Gingivitis B4GALT7 11285 beta-1,4-galactosyltransferase 7 Q9UBV7
C0029422 Osteochondrodysplasias B4GALT7 11285 beta-1,4-galactosyltransferase 7 Q9UBV7
C0009363 Congenital ocular coloboma (disorder) B4GALT7 11285 beta-1,4-galactosyltransferase 7 Q9UBV7
C0003873 Rheumatoid Arthritis B4GALT7 11285 beta-1,4-galactosyltransferase 7 Q9UBV7
C2239176 Liver carcinoma B4GALT7 11285 beta-1,4-galactosyltransferase 7 Q9UBV7
C0015300 Exophthalmos B4GALT7 11285 beta-1,4-galactosyltransferase 7 Q9UBV7
C2931009 Congenital disorder of glycosylation type 2D B4GALT7 11285 beta-1,4-galactosyltransferase 7 Q9UBV7
C0023787 Lipodystrophy B4GALT7 11285 beta-1,4-galactosyltransferase 7 Q9UBV7
C0009402 Colorectal Carcinoma B4GALT6 9331 beta-1,4-galactosyltransferase 6 Q9UBX8
C0037268 Skin Abnormalities B4GALT6 9331 beta-1,4-galactosyltransferase 6 Q9UBX8
C0026769 Multiple Sclerosis B4GALT6 9331 beta-1,4-galactosyltransferase 6 Q9UBX8
C0022661 Kidney Failure, Chronic KL 9365 klotho Q9UEF7
C0022658 Kidney Diseases KL 9365 klotho Q9UEF7
C0020503 Hyperparathyroidism, Secondary KL 9365 klotho Q9UEF7
C0029456 Osteoporosis KL 9365 klotho Q9UEF7

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Last updated: August 19, 2024