GYPB, glycophorin B (MNS blood group), 2994

N. diseases: 80; N. variants: 1
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0410528
Disease: Skeletal dysplasia
Skeletal dysplasia
0.010 GeneticVariation disease BEFREE This is the second known instance of a male infant with omphalocele and this skeletal dysplasia born to a woman with MNS. 7158644 1982