GYPB, glycophorin B (MNS blood group), 2994

N. diseases: 80; N. variants: 1
Disease: Congenital disorder of glycosylation type 1A ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0349653
Disease: Congenital disorder of glycosylation type 1A
Congenital disorder of glycosylation type 1A 		0.010 Biomarker disease BEFREE Band 3 glycoprotein and glycophorin A from erythrocytes of children with congenital disorder of glycosylation type-Ia are underglycosylated. 11680873 2001