D69.41

Evans syndrome

Billable / specificHCC V28 112

D69.41 is a billable, specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes in FY2027.

Excludes1

Not coded here — never report together with this code.

  • transient neonatal thrombocytopenia (P61.0) (from D69.4)
  • Wiskott-Aldrich syndrome (D82.0) (from D69.4)
  • benign hypergammaglobulinemic purpura (D89.0) (from D69)
  • cryoglobulinemic purpura (D89.1) (from D69)
  • essential (hemorrhagic) thrombocythemia (D47.3) (from D69)
  • hemorrhagic thrombocythemia (D47.3) (from D69)
  • purpura fulminans (D65) (from D69)
  • thrombotic thrombocytopenic purpura (M31.19) (from D69)
  • Waldenström hypergammaglobulinemic purpura (D89.0) (from D69)

Excludes2

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

  • autoimmune disease (systemic) NOS (M35.9) (from D69)
  • certain conditions originating in the perinatal period (P00-P96) (from D69)
  • complications of pregnancy, childbirth and the puerperium (O00-O9A) (from D69)
  • congenital malformations, deformations and chromosomal abnormalities (Q00-Q99) (from D69)
  • endocrine, nutritional and metabolic diseases (E00-E88) (from D69)
  • human immunodeficiency virus [HIV] disease (B20) (from D69)
  • injury, poisoning and certain other consequences of external causes (S00-T88) (from D69)
  • neoplasms (C00-D49) (from D69)
  • symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94) (from D69)

Also known as

  • Syndrome, Evans

Parent code

  • D69.4Other primary thrombocytopeniaHeader

Related codes

  • D69.42Congenital and hereditary thrombocytopenia purpuraBillable
  • D69.49Other primary thrombocytopeniaBillable

Browse