Disease: ABO incompatibility ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
ABO incompatibility
CUI: C0860218
Disease: ABO incompatibility
0.010 GeneticVariation BEFREE UGT1A1 gene promoter polymorphism and G71R mutation are possible risk factors for Turkish neonates with DC(-) ABO incompatibility and unexplained hyperbilirubinemia. 27842454 2017