F2, coagulation factor II, thrombin, 2147

N. diseases: 490; N. variants: 42
Disease: Familial (FPAH) ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH) 		0.040 Biomarker disease BEFREE Though several genes, such as antithrombin, protein C, protein S, factor V, and prothrombin are associated with the familial clustering of VTE, these loci only partially explain the familial aggregation of VTE. 27764883 2016
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH) 		0.040 GeneticVariation disease BEFREE The most common forms of familial thrombophilia are factor V Leiden (FVL) and prothrombin mutation (PTM). 23054468 2013
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH) 		0.040 Biomarker disease BEFREE We have examined the prothrombin gene as a candidate gene for venous thrombosis in selected patients with a documented familial history of venous thrombophilia. 8916933 1996
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH) 		0.040 GeneticVariation disease BEFREE Familial haemostatic defect associated with reduced prothrombin consumption. 7378303 1980