Disease: Abruptio Placentae ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0000832
Disease: Abruptio Placentae
Abruptio Placentae 		0.310 GeneticVariation phenotype LHGDN In this population, there was an association between the homozygous mutant form of BHMT (742G-->A) polymorphism and increased risk for placental abruption. 17376725 2007
CUI: C0000832
Disease: Abruptio Placentae
Abruptio Placentae 		0.310 Biomarker phenotype CTD_human In this population, there was an association between the homozygous mutant form of BHMT (742G-->A) polymorphism and increased risk for placental abruption. 17376725 2007