D60.8

Other acquired pure red cell aplasias

Billable / specificHCC V28 109

D60.8 is a billable, specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes in FY2027.

Inclusion terms

Includes (from D60)

  • red cell aplasia (acquired) (adult) (with thymoma)

Excludes1

Not coded here — never report together with this code.

  • congenital red cell aplasia (D61.01) (from D60)

Excludes2

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

  • autoimmune disease (systemic) NOS (M35.9) (from D60)
  • certain conditions originating in the perinatal period (P00-P96) (from D60)
  • complications of pregnancy, childbirth and the puerperium (O00-O9A) (from D60)
  • congenital malformations, deformations and chromosomal abnormalities (Q00-Q99) (from D60)
  • endocrine, nutritional and metabolic diseases (E00-E88) (from D60)
  • human immunodeficiency virus [HIV] disease (B20) (from D60)
  • injury, poisoning and certain other consequences of external causes (S00-T88) (from D60)
  • neoplasms (C00-D49) (from D60)
  • symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94) (from D60)

Also known as

  • Anemia, aplastic, red cell, specified type NEC
  • Aplasia, red cell, specified type NEC

Parent code

  • D60Acquired pure red cell aplasia [erythroblastopenia]Header

Related codes

  • D60.0Chronic acquired pure red cell aplasiaBillable
  • D60.1Transient acquired pure red cell aplasiaBillable
  • D60.9Acquired pure red cell aplasia, unspecifiedBillable

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