Parent term(s)
Term with siblings
acquired von Willebrand syndrome
autosomal hemophilia A
Bernard-Soulier syndrome +
blood platelet disease +
congenital afibrinogenemia
factor V deficiency
factor VII deficiency
factor VIII deficiency
factor X deficiency
factor XI deficiency
factor XII deficiency
factor XIII deficiency
hemophilia B
hemorrhagic disease +
hereditary combined deficiency of vitamin K-dependent clotting factors +
high molecular weight kininogen deficiency
Scott syndrome
von Willebrand's disease +
thrombophilia +
acquired von Willebrand syndrome
autosomal hemophilia A
Bernard-Soulier syndrome +
blood platelet disease +
congenital afibrinogenemia
factor V deficiency
factor VII deficiency
factor VIII deficiency
factor X deficiency
factor XI deficiency
factor XII deficiency
factor XIII deficiency
hemophilia B
hemorrhagic disease +
hereditary combined deficiency of vitamin K-dependent clotting factors +
high molecular weight kininogen deficiency
Scott syndrome
von Willebrand's disease +
Child term(s)
antithrombin III deficiency
disseminated intravascular coagulation +
heparin cofactor II deficiency
protein C deficiency +
protein S deficiency +
prothrombin deficiency
prothrombin thrombophilia
thrombophilia due to activated protein C resistance
thrombophilia due to decreased release of PLAT
thrombophilia due to HRG deficiency
thrombophilia due to thrombin defect
thrombophilia due to thrombomodulin defect
thrombotic thrombocytopenic purpura
X-linked thrombophilia due to factor IX defect
antithrombin III deficiency
disseminated intravascular coagulation +
heparin cofactor II deficiency
protein C deficiency +
protein S deficiency +
prothrombin deficiency
prothrombin thrombophilia
thrombophilia due to activated protein C resistance
thrombophilia due to decreased release of PLAT
thrombophilia due to HRG deficiency
thrombophilia due to thrombin defect
thrombophilia due to thrombomodulin defect
thrombotic thrombocytopenic purpura
X-linked thrombophilia due to factor IX defect
denotes an 'is-a' relationship