Section D65-D69 | Coagulation defects purpura other

D65

Disseminated intravascular coagulation [defibrination syndrome]

D66

Hereditary factor VIII deficiency

D67

Hereditary factor IX deficiency

D68

Code hierarchy

D68 Other coagulation defects
- D68.0 Von Willebrand disease
  - D68.00 Von Willebrand disease, unspecified
  - D68.01 Von Willebrand disease, type 1
  - D68.02 Von Willebrand disease, type 2
    - D68.020 Von Willebrand disease, type 2A
    - D68.021 Von Willebrand disease, type 2B
    - D68.022 Von Willebrand disease, type 2M
    - D68.023 Von Willebrand disease, type 2N
    - D68.029 Von Willebrand disease, type 2, unspecified
  - D68.03 Von Willebrand disease, type 3
  - D68.04 Acquired von Willebrand disease
  - D68.09 Other von Willebrand disease
- D68.1 Hereditary factor XI deficiency
- D68.2 Hereditary deficiency of other clotting factors
- D68.3 Hemorrhagic disorder due to circulating anticoagulants
  - D68.31 Hemorrhagic disorder due to intrinsic circulating anticoagulants, antibodies, or inhibitors
    - D68.311 Acquired hemophilia
    - D68.312 Antiphospholipid antibody with hemorrhagic disorder
    - D68.318 Other hemorrhagic disorder due to intrinsic circulating anticoagulants, antibodies, or inhibitors
  - D68.32 Hemorrhagic disorder due to extrinsic circulating anticoagulants
- D68.4 Acquired coagulation factor deficiency
- D68.5 Primary thrombophilia
  - D68.51 Activated protein C resistance
  - D68.52 Prothrombin gene mutation
  - D68.59 Other primary thrombophilia
- D68.6 Other thrombophilia
  - D68.61 Antiphospholipid syndrome
  - D68.62 Lupus anticoagulant syndrome
  - D68.69 Other thrombophilia
- D68.8 Other specified coagulation defects
- D68.9 Coagulation defect, unspecified

Other coagulation defects

D69

Code hierarchy

D69 Purpura and other hemorrhagic conditions
- D69.0 Allergic purpura
- D69.1 Qualitative platelet defects
- D69.2 Other nonthrombocytopenic purpura
- D69.3 Immune thrombocytopenic purpura
- D69.4 Other primary thrombocytopenia
  - D69.41 Evans syndrome
  - D69.42 Congenital and hereditary thrombocytopenia purpura
  - D69.49 Other primary thrombocytopenia
- D69.5 Secondary thrombocytopenia
  - D69.51 Posttransfusion purpura
  - D69.59 Other secondary thrombocytopenia
- D69.6 Thrombocytopenia, unspecified
- D69.8 Other specified hemorrhagic conditions
- D69.9 Hemorrhagic condition, unspecified

Purpura and other hemorrhagic conditions

Section D65-D69 Coagulation defects, purpura and other hemorrhagic conditions D65-D69

Code List:

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Code hierarchy