1. D68 Other coagulation defects

    1. D68.0 Von Willebrand disease

      1. D68.00 Von Willebrand disease, unspecified

      2. D68.01 Von Willebrand disease, type 1

        Inclusion term(s):

        • Partial quantitative deficiency of von Willebrand factor
        • Type 1C von Willebrand disease
      3. D68.02 Von Willebrand disease, type 2

        Inclusion term(s):

        • Qualitative defects of von Willebrand factor
        • D68.020 Von Willebrand disease, type 2A

          Inclusion term(s):

          • Qualitative defects of von Willebrand factor with decreased platelet adhesion and selective deficiency of high-molecular-weight multimers
        • D68.021 Von Willebrand disease, type 2B

          Inclusion term(s):

          • Qualitative defects of von Willebrand factor with high-molecular-weight von Willebrand factor loss
          • Qualitative defects of von Willebrand factor with hyper-adhesive forms
          • Qualitative defects of von Willebrand factor with increased affinity for platelet glycoprotein lb
        • D68.022 Von Willebrand disease, type 2M

          Inclusion term(s):

          • Qualitative defects of von Willebrand factor with defective platelet adhesion with a normal size distribution of von Willebrand factor multimers
        • D68.023 Von Willebrand disease, type 2N

          Inclusion term(s):

          • Qualitative defects of von Willebrand factor with defective von Willebrand factor to factor VIII binding
          • Qualitative defects of von Willebrand factor with markedly decreased affinity for factor VIII
        • D68.029 Von Willebrand disease, type 2, unspecified

          Inclusion term(s):

          • Qualitative defect in von Willebrand factor function, with no further subtyping
      4. D68.03 Von Willebrand disease, type 3

        Inclusion term(s):

        • (Near) complete absence of von Willebrand factor
        • Total quantitative deficiency of von Willebrand factor
      5. D68.04 Acquired von Willebrand disease

        Inclusion term(s):

        • Acquired von Willebrand syndrome
      6. D68.09 Other von Willebrand disease

        Inclusion term(s):

        • Platelet-type von Willebrand disease
        • Pseudo-von Willebrand disease
    2. D68.1 Hereditary factor XI deficiency

      Inclusion term(s):

      • Hemophilia C
      • Plasma thromboplastin antecedent [PTA] deficiency
      • Rosenthal's disease
    3. D68.2 Hereditary deficiency of other clotting factors

      Inclusion term(s):

      • AC globulin deficiency
      • Congenital afibrinogenemia
      • Deficiency of factor I [fibrinogen]
      • Deficiency of factor II [prothrombin]
      • Deficiency of factor V [labile]
      • Deficiency of factor VII [stable]
      • Deficiency of factor X [Stuart-Prower]
      • Deficiency of factor XII [Hageman]
      • Deficiency of factor XIII [fibrin stabilizing]
      • Dysfibrinogenemia (congenital)
      • Hypoproconvertinemia
      • Owren's disease
      • Proaccelerin deficiency
    4. D68.3 Hemorrhagic disorder due to circulating anticoagulants

      1. D68.31 Hemorrhagic disorder due to intrinsic circulating anticoagulants, antibodies, or inhibitors

        • D68.311 Acquired hemophilia

          Inclusion term(s):

          • Autoimmune hemophilia
          • Autoimmune inhibitors to clotting factors
          • Secondary hemophilia
        • D68.312 Antiphospholipid antibody with hemorrhagic disorder

          Inclusion term(s):

          • Lupus anticoagulant (LAC) with hemorrhagic disorder
          • Systemic lupus erythematosus [SLE] inhibitor with hemorrhagic disorder
        • D68.318 Other hemorrhagic disorder due to intrinsic circulating anticoagulants, antibodies, or inhibitors

          Inclusion term(s):

          • Antithromboplastinemia
          • Antithromboplastinogenemia
          • Hemorrhagic disorder due to intrinsic increase in antithrombin
          • Hemorrhagic disorder due to intrinsic increase in anti-VIIIa
          • Hemorrhagic disorder due to intrinsic increase in anti-IXa
          • Hemorrhagic disorder due to intrinsic increase in anti-XIa
      2. D68.32 Hemorrhagic disorder due to extrinsic circulating anticoagulants

        Inclusion term(s):

        • Drug-induced hemorrhagic disorder
        • Hemorrhagic disorder due to increase in anti-IIa
        • Hemorrhagic disorder due to increase in anti-Xa
        • Hyperheparinemia
    5. D68.4 Acquired coagulation factor deficiency

      Inclusion term(s):

      • Deficiency of coagulation factor due to liver disease
      • Deficiency of coagulation factor due to vitamin K deficiency
    6. D68.5 Primary thrombophilia

      Inclusion term(s):

      • Primary hypercoagulable states
      1. D68.51 Activated protein C resistance

        Inclusion term(s):

        • Factor V Leiden mutation
      2. D68.52 Prothrombin gene mutation

      3. D68.59 Other primary thrombophilia

        Inclusion term(s):

        • Antithrombin III deficiency
        • Hypercoagulable state NOS
        • Primary hypercoagulable state NEC
        • Primary thrombophilia NEC
        • Protein C deficiency
        • Protein S deficiency
        • Thrombophilia NOS
    7. D68.6 Other thrombophilia

      Inclusion term(s):

      • Other hypercoagulable states
      1. D68.61 Antiphospholipid syndrome

        Inclusion term(s):

        • Anticardiolipin syndrome
        • Antiphospholipid antibody syndrome
      2. D68.62 Lupus anticoagulant syndrome

        Inclusion term(s):

        • Lupus anticoagulant
        • Presence of systemic lupus erythematosus [SLE] inhibitor
      3. D68.69 Other thrombophilia

        Inclusion term(s):

        • COVID-19 associated hypercoagulability
        • Hypercoagulable states NEC
        • Secondary hypercoagulable state NOS
    8. D68.8 Other specified coagulation defects

      Inclusion term(s):

      • COVID-19 associated coagulopathy
    9. D68.9 Coagulation defect, unspecified

Abbreviations used here:

NEC Not elsewhere classifiable
This abbreviation in the Tabular List represents “other specified”. When a specific code is not available for a condition, the Tabular List includes an NEC entry under a code to identify the code as the “other specified” code.

NOS Not otherwise specified
This abbreviation is the equivalent of unspecified.