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D68.5

ICD-10-CM 2027

Primary thrombophilia

Child codes

  • D68.51 – Activated protein C resistance
  • D68.52 – Prothrombin gene mutation
  • D68.59 – Other primary thrombophilia

Sibling codes

  • D68.0 – 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
  • D68.4 – Acquired coagulation factor deficiency
  • D68.6 – Other thrombophilia
  • D68.8 – Other specified coagulation defects
  • D68.9 – Coagulation defect, unspecified

Excludes1

  • antiphospholipid syndrome (D68.61)
  • lupus anticoagulant (D68.62)
  • secondary activated protein C resistance (D68.69)
  • secondary antiphospholipid antibody syndrome (D68.69)
  • secondary lupus anticoagulant with hypercoagulable state (D68.69)
  • secondary systemic lupus erythematosus [SLE] inhibitor with hypercoagulable state (D68.69)
  • systemic lupus erythematosus [SLE] inhibitor finding without diagnosis (R76.0)
  • systemic lupus erythematosus [SLE] inhibitor with hemorrhagic disorder (D68.312)
  • thrombotic thrombocytopenic purpura (M31.19)

Inclusion terms

  • Primary hypercoagulable states

Inherited from D68: Other coagulation defects

Excludes1

  • abnormal coagulation profile NOS (R79.1)

Excludes2

  • 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)

Part of: D68: Other coagulation defects