Parent term(s)
Term with siblings
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
thrombophilia +
von Willebrand's disease +
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
thrombophilia +
von Willebrand's disease +
Child term(s)
denotes an 'is-a' relationship