Q89.01

Asplenia (congenital)

Billable / specificPOA exempt

Q89.01 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 Q89)

  • Note: Codes from this chapter are not for use on maternal records

Excludes1

Not coded here — never report together with this code.

  • isomerism of atrial appendages (with asplenia or polysplenia) (Q20.6) (from Q89.0)

Excludes2

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

  • inborn errors of metabolism (E70-E88) (from Q89)

Also known as

  • Absence, spleen
  • Agenesis, spleen
  • Anomaly, anomalous, spleen, agenesis
  • Aplasia, spleen
  • Asplenia
  • Ivemark's syndrome
  • Syndrome, Ivemark's
  • Syndrome, splenic, agenesis

Parent code

  • Q89.0Congenital absence and malformations of spleenHeader

Related codes

  • Q89.09Congenital malformations of spleenBillable

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