Gene: B4GALT1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2683
Gene Symbol: B4GALT1
B4GALT1 		0.110 Biomarker disease LHGDN Deficiency of UDP-galactose:N-acetylglucosamine beta-1,4-galactosyltransferase I causes the congenital disorder of glycosylation type IId. 11901181 2002
Entrez Id: 2683
Gene Symbol: B4GALT1
B4GALT1 		0.110 Biomarker disease HPO