F2, coagulation factor II, thrombin, 2147

N. diseases: 490; N. variants: 42
Disease: Dysfibrinogenemia ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1260903
Disease: Dysfibrinogenemia
Dysfibrinogenemia 		0.010 GeneticVariation disease BEFREE Some of the hematological risk factors implicated in the development of coronary heart disease include antithrombin III deficiency, protein C and protein S deficiency, factor V Leiden mutation, prothrombin gene (20210A) mutation hyperhomocystinaemia, elevated factor VIII levels, plasminogen activator inhibitor type 1 and dysfibrinogenaemia. 12444311 2002