Source: LHGDN

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2683
Gene Symbol: B4GALT1
B4GALT1
CUI: C0020255
Disease: Hydrocephalus
Hydrocephalus 		0.110 Biomarker LHGDN Deficiency of UDP-galactose:N-acetylglucosamine beta-1,4-galactosyltransferase I causes the congenital disorder of glycosylation type IId. 11901181

2002