Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism

Coagulation defects, purpura and other hemorrhagic conditions (D65-D69)

• Other coagulation defects (D68)

  • 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 intrns circ anticoag,antib,inhib
  • D68.311 - Acquired hemophilia
  • D68.312 - Antiphospholipid antibody with hemorrhagic disorder
  • D68.318 - Oth hemorrhagic disord d/t intrns circ anticoag,antib,inhib
  • D68.32 - Hemorrhagic disord d/t 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