SLC10A2, solute carrier family 10 member 2, 6555

N. diseases: 66; N. variants: 9
Disease: Erythroblastosis, Fetal ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0014761
Disease: Erythroblastosis, Fetal
Erythroblastosis, Fetal 		0.010 Biomarker disease BEFREE Investigation of a mild case of hemolytic disease of the newborn has led to recognition of a 'new' low-incidence red cell antigen, WARR (ISBT No.700.55). 7625077 1995