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Coagulation Defects

  • Congenital factor VIII disorder 286.X
    • including antihemophilic globulin (AHG) deficiency, hemophilia (NOS, A, classical, familial, hereditary); subhemophilia
  • Congenital factor IX disorder 286.X
    • including Christmas disease, deficiency:plasma thromboplastin component (PTC), hemophilia B
  • Congenital factor XI deficiency 286.X
    • including hemophilia C, plasma thromboplastin antecedent (PTA) deficiency, Rosenthal's disease
  • Congenital deficiency of other clotting factors  286.X
    • including congenital afibrinogenemia, dysfibrinogenemia, deficiency of factor I (fibrinogen), II (prothrombin), V (labile), VII (stable), X (Stuart-Prower), XII (Hageman), XIII (fibrin stabilizing), Laki-Lorand factor, proaccelerin; Owren's disease, Stuart-Prower disease, constitutional dysprothrombinemia, hypoproconvertinemia, hypoprothrombinemia, parahemophilia
  • von Willebrand's disease 286.X
    • including angiohemophilia (A, B), constitutional thrombopathy, factor VIII deficiency with vascular defect, pseudohemophilia type B, vascular hemophilia, von Willebrand's (-Jürgens') disease
  • Hemorrhagic disorder due to intrinsic circulating anticoagulants  286.X
    • including antithrombinemia, antithromboplastinemia, antithromboplastinogenemia, hyperheparinemia, increase in anti-VIIIa, anti-IXa, anti-Xa, anti-XIa, antithrombin; systemic lupus erythematosus (SLE) inhibitor, secondary hemophilia
  • Acquired coagulation factor deficiency  286.X (E)
    • including deficiency of coagulation factor due to liver disease, vitamin K deficiency; hypoprothrombinemia, acquired
  • Other and unspecified coagulation defects  286.X
    • including coagulation disorder NOS