D68.5

Primary thrombophilia

Non-billable header

D68.5 is a non-billable header code. Use one of the more specific codes below.

Inclusion terms

Applicable to

  • Primary hypercoagulable states

Excludes1

Not coded here — never report together with this code.

  • 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)
  • abnormal coagulation profile NOS (R79.1) (from D68)

Excludes2

Not included here — may be reported together when both conditions exist.

  • autoimmune disease (systemic) NOS (M35.9) (from D68)
  • certain conditions originating in the perinatal period (P00-P96) (from D68)
  • complications of pregnancy, childbirth and the puerperium (O00-O9A) (from D68)
  • congenital malformations, deformations and chromosomal abnormalities (Q00-Q99) (from D68)
  • endocrine, nutritional and metabolic diseases (E00-E88) (from D68)
  • human immunodeficiency virus [HIV] disease (B20) (from D68)
  • injury, poisoning and certain other consequences of external causes (S00-T88) (from D68)
  • neoplasms (C00-D49) (from D68)
  • symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94) (from D68)
  • coagulation defects complicating abortion or ectopic or molar pregnancy (O00-O07, O08.1) (from D68)
  • coagulation defects complicating pregnancy, childbirth and the puerperium (O45.0, O46.0, O67.0, O72.3) (from D68)

Also known as

  • Primary hypercoagulable states

Parent code

  • D68Other coagulation defectsHeader

More specific codes D68.5

  • D68.51Activated protein C resistanceBillable
  • D68.52Prothrombin gene mutationBillable
  • D68.59Other primary thrombophiliaBillable

Related codes

  • D68.0Von Willebrand diseaseHeader
  • D68.1Hereditary factor XI deficiencyBillable
  • D68.2Hereditary deficiency of other clotting factorsBillable
  • D68.3Hemorrhagic disorder due to circulating anticoagulantsHeader
  • D68.4Acquired coagulation factor deficiencyBillable
  • D68.6Other thrombophiliaHeader
  • D68.8Other specified coagulation defectsBillable
  • D68.9Coagulation defect, unspecifiedBillable

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