D69

Purpura and other hemorrhagic conditions

Non-billable header

D69 is a non-billable header code. Use one of the more specific codes below.

Excludes1

Not coded here — never report together with this code.

  • benign hypergammaglobulinemic purpura (D89.0)
  • cryoglobulinemic purpura (D89.1)
  • essential (hemorrhagic) thrombocythemia (D47.3)
  • hemorrhagic thrombocythemia (D47.3)
  • purpura fulminans (D65)
  • thrombotic thrombocytopenic purpura (M31.19)
  • Waldenström hypergammaglobulinemic purpura (D89.0)

Excludes2

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

  • autoimmune disease (systemic) NOS (M35.9)
  • certain conditions originating in the perinatal period (P00-P96)
  • complications of pregnancy, childbirth and the puerperium (O00-O9A)
  • congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
  • endocrine, nutritional and metabolic diseases (E00-E88)
  • human immunodeficiency virus [HIV] disease (B20)
  • injury, poisoning and certain other consequences of external causes (S00-T88)
  • neoplasms (C00-D49)
  • symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)

More specific codes D69

  • D69.0Allergic purpuraBillable
  • D69.1Qualitative platelet defectsHeader
  • D69.2Other nonthrombocytopenic purpuraBillable
  • D69.3Immune thrombocytopenic purpuraBillable
  • D69.4Other primary thrombocytopeniaHeader
  • D69.5Secondary thrombocytopeniaHeader
  • D69.6Thrombocytopenia, unspecifiedBillable
  • D69.8Other specified hemorrhagic conditionsBillable
  • D69.9Hemorrhagic condition, unspecifiedBillable

Related codes

  • D65Disseminated intravascular coagulation [defibrination syndrome]Billable
  • D66Hereditary factor VIII deficiencyBillable
  • D67Hereditary factor IX deficiencyBillable
  • D68Other coagulation defectsHeader

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