F2, coagulation factor II, thrombin, 2147

N. diseases: 490; N. variants: 42
Disease: Acute myocardial infarction ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0155626
Disease: Acute myocardial infarction
Acute myocardial infarction 		0.040 GeneticVariation disease BEFREE We showed an increased risk of AMI with factor V (FV) Leiden and prothrombin G20210A heterozygosity. 25693916 2016
CUI: C0155626
Disease: Acute myocardial infarction
Acute myocardial infarction 		0.040 GeneticVariation disease BEFREE Here we report data strongly suggesting that at least the FII G20210A polymorphism might be considered an important risk factor for acute myocardial infarction in aged patients (55-80 years old). 21918818 2011
CUI: C0155626
Disease: Acute myocardial infarction
Acute myocardial infarction 		0.040 GeneticVariation disease BEFREE Arterial thrombosis and acute myocardial infarction with angiographically normal coronary arteries in a woman heterozygous for both factor V Leiden and prothrombin mutation. 21958997 2011
CUI: C0155626
Disease: Acute myocardial infarction
Acute myocardial infarction 		0.040 GeneticVariation disease BEFREE A patient with hemophilia A is reported who had an acute myocardial infarction and in whom investigation for hereditary thrombophilia showed a prothrombotic molecular defect, the G20210A prothrombin mutation. 16015425 2005