Disease: Heart Septal Defects ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0018816
Disease: Heart Septal Defects
Heart Septal Defects 		0.020 GeneticVariation group BEFREE Meanwhile, more patients were carriers of the ABCB1 CC/CT genotypes, which were significantly associated with an increased risk of septal defects (OR 2.414; 95 % CI 1.418-4.110; P = 0.001). 24740628 2014
CUI: C0018816
Disease: Heart Septal Defects
Heart Septal Defects 		0.020 GeneticVariation group BEFREE The C3435T polymorphism in the ABCB1 gene of fetus increases the risks of CHD in a Han Chinese population when the mothers are exposed to phthalates and alkylphenolic compounds during the periconceptional period, particularly for septal defects. 23874772 2013