GYPE, glycophorin E (MNS blood group), 2996

N. diseases: 83; N. variants: 0
Disease: Congenital disorder of glycosylation type 1s ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4317295
Disease: Congenital disorder of glycosylation type 1s
Congenital disorder of glycosylation type 1s 		0.010 Biomarker disease BEFREE A possible molecular mechanism of hypo- and unglycosylation of band 3 and glycophorin A, respectively, in CDG is discussed. 11680873 2001