This page needs to be proofread.
of coagulation factor due to liver disease
- Deficiency of coagulation factor due to vitamin K deficiency
- Excludes1: vitamin K deficiency of newborn (P53)
- D68.5 Primary thrombophilia
- Primary hypercoagulable states
- Excludes1: lupus anticoagulant (D68.62)
- thrombotic thrombocytopenic purpura (M31.1)
- D68.51 Activated protein C resistance
- Factor V Leiden mutation
- D68.52 Prothrombin gene mutation
- D68.59 Other primary thrombophilia
- Antithrombin III deficiency
- Hypercoagulable state NOS
- Primary hypercoagulable state NEC
- Primary thrombophilia NEC
- Protein C deficiency
- Protein S deficiency
- Thrombophilia NOS
- D68.6 Other thrombophilia
- Other hypercoagulable states
- Excludes1: diffuse or disseminated intravascular coagulation [DIC] (D65)
- heparin induced thrombocytopenia (HIT) (D75.82)
- hyperhomocysteinemia (E72.11)
- D68.61 Anticardiolipin syndrome
- Antiphospholipid syndrome
- Excludes1: lupus anticoagulant syndrome (D68.62)
- D68.62 Lupus anticoagulant syndrome
- Lupus anticoagulant
- Presence of systemic lupus erythematosus [SLE] inhibitor
- Excludes1: anticardiolipin syndrome (D68.61)
- antiphospholipid syndrome (D68.61)
- D68.69 Other thrombophilia
- Hypercoagulable states NEC
- Secondary hypercoagulable state NOS
- D68.8 Other specified coagulation defects
- Excludes1: hemorrhagic disease of newborn (P53)
- D68.9 Coagulation defect, unspecified
D69 Purpura and other hemorrhagic conditions
- Excludes1: benign hypergammaglobulinemic purpura (D89.0)
- cryoglobulinemic purpura (D89.1)
- essential (hemorrhagic) thrombocythemia (D47.3)
- hemorrhagic thrombocythemia (D47.3)
- purpura fulminans (D65)
- thrombotic thrombocytopenic purpura (M31.1)
- Waldenström's hypergammaglobulinemic purpura (D89.0)
- D69.
