F2, coagulation factor II, thrombin, 2147

N. diseases: 490; N. variants: 42
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0007786
Disease: Brain Ischemia
Brain Ischemia
0.320 Biomarker disease LHGDN Prothrombotic mutations as risk factors for cryptogenic ischemic cerebrovascular events in young subjects with patent foramen ovale. 17525392 2007
CUI: C0007786
Disease: Brain Ischemia
Brain Ischemia
0.320 Biomarker disease CTD_human Meta-analysis of genetic studies in ischemic stroke: thirty-two genes involving approximately 18,000 cases and 58,000 controls. 15534175 2004
CUI: C0007786
Disease: Brain Ischemia
Brain Ischemia
0.320 GeneticVariation disease LHGDN Prothrombin G20210A mutation, but not factor V Leiden, is a risk factor in patients with persistent foramen ovale and otherwise unexplained cerebral ischemia. 12766367 2003
CUI: C0007786
Disease: Brain Ischemia
Brain Ischemia
0.320 Biomarker disease CTD_human Thrombin exacerbates brain edema in focal cerebral ischemia. 14753426 2003