Other coagulation defects - D68
Type 1 Excludes
- abnormal coagulation profile NOS (R79.1)
Type 2 Excludes
- coagulation defects complicating abortion or ectopic or molar pregnancy (O00-O07, O08.1)
- coagulation defects complicating pregnancy, childbirth and the puerperium (O45.0, O46.0, O67.0, O72.3)
Codes
- 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