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Q89.01

Q89.01Asplenia (congenital)

Billable / specific codeICD-10-CMPOA exempt

Q89.01 is a billable, specific ICD-10-CM code for asplenia (congenital). It is valid for submission on a claim.

Excludes1 inherited from the categories above Q89.01

These are not written on Q89.01, but they bind it: a note on a category applies to every code beneath it. Billing Q89.01 with anything listed here is a denial.

Written on Q89.0 Congenital absence and malformations of spleen

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

Other codes that can never be billed with Q89.01

These codes carry an Excludes1 note pointing at Q89.01. The conflict binds both ways, but ICD-10-CM only writes it down on one side — so you would not find this by reading Q89.01 alone.

Risk adjustment

Q89.01 does not map to an HCC and does not risk-adjust under CMS-HCC V28. That is normal — most ICD-10 codes do not. It still needs to be coded correctly; it just will not move a RAF score.

Medicare coverage

Q89.01 is named in 5 Medicare coverage policies 5 listing it as supporting medical necessity. Which of them applies to you depends on your Medicare contractor, and coverage genuinely differs by state.

  • A56421Billing and Coding: CT of the Abdomen and Pelvis
  • A56781Billing and Coding: Transthoracic Echocardiography (TTE)
  • A56781Billing and Coding: Transthoracic Echocardiography (TTE)
  • A57306Billing and Coding: Transthoracic Echocardiography (TTE)

How Q89.01 is indexed

Coders do not find codes by browsing the tabular list — they look them up in the alphabetic index, under the word the physician wrote. These are the index entries that lead here, so you can see which chart wordings map to Q89.01.

  • Asplenia(congenital)
  • Ivemark's syndrome(asplenia with congenital heart disease)
  • Absencespleen(congenital)
  • Agenesisspleen
  • Aplasiaspleen
  • SyndromeIvemark's
  • Anomaly, anomalousspleenagenesis
  • Syndromesplenicagenesis

Code history

Q89.01 has not changed since FY2024 — no addition, revision or deletion across the three most recent ICD-10-CM releases.

Related codes at this level

Codes that share Q89.0. If Q89.01 is not quite right, the correct code is usually one of these.

Questions about Q89.01

Is Q89.01 a billable ICD-10-CM code?
Yes. Q89.01 is a billable, specific ICD-10-CM code and is valid for submission on a claim.
Where does Q89.01 sit in the tabular list?
Congenital malformations, deformations and chromosomal abnormalities (Q00-QA0), in the block Other congenital malformations (Q80-Q89).
What cannot be coded together with Q89.01?
Q89.01 carries Excludes1 notes, which means the conditions they list can never be coded together with it on the same encounter. Some are written on the categories above Q89.01 (Q89.0) and apply to it just the same.
ICD-10-CMFY2026-Apr· effective April 1, 2026

Loaded directly from the CMS/NCHS ICD-10-CM public-domain release — see data sources and our editorial policy. If this page disagrees with the CMS tabular list, this page is wrong. Reference information for professional coders; not medical or billing advice.