F2, coagulation factor II, thrombin, 2147

N. diseases: 61; N. variants: 24
Source: CURATED ×
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0040053
Disease: Thrombosis
Thrombosis
0.580 Biomarker phenotype CTD_human Cerebral venous sinus thrombosis as a recurrent thrombotic event in a patient with heterozygous prothrombin G20210A genotype after discontinuation of oral anticoagulation therapy: how long should we treat these patients with warfarin? 17245631 2007
CUI: C0040053
Disease: Thrombosis
Thrombosis
0.580 Biomarker phenotype CTD_human Deep vein thrombosis during enoxaparin prophylactic treatment in a young pregnant woman homozygous for factor V Leiden and heterozygous for the G127-->a mutation in the thrombomodulin gene. 11132655 2000
CUI: C0040053
Disease: Thrombosis
Thrombosis
0.580 Biomarker phenotype CTD_human Pharmacological effects of a novel recombinant hirudin, CX-397, in vivo and in vitro: comparison with recombinant hirudin variant-1, heparin, and argatroban. 10064001 1999
CUI: C0040053
Disease: Thrombosis
Thrombosis
0.580 Biomarker phenotype CTD_human Effect of sodium pentosan polysulphate on the thrombogenicity of prothrombin complex concentrates. 1279834 1992