Question 1

What is ICD-10 code Q87.88?

Accepted Answer

Q87.88 is the ICD-10-CM diagnosis code for ctnnb1 syndrome. CTNNB1 syndrome is a rare genetic disorder caused by mutations in the CTNNB1 gene, resulting in developmental delay, intellectual disability, and distinctive features. Q87.88 sits in the ICD-10-CM chapter for congenital malformations, deformations, chromosomal abnormalities, and genetic disorders (q00-qa0), within the section covering other congenital malformations (q80-q89).

Q87.88 is a billable ICD-10-CM code but does not map to a payment HCC under the CMS-HCC V28, V24, ESRD, or RxHCC risk adjustment models. It can be reported on Medicare Advantage encounter data submissions but it does not contribute to a beneficiary's RAF score and therefore does not affect risk-adjusted payments to the plan.

Verify genetic testing documentation supports CTNNB1 mutation diagnosis.

Question 2

Is Q87.88 an HCC code?

Accepted Answer

No. Q87.88 is a billable ICD-10-CM code but does not map to any payment HCC category under the CMS-HCC V28, V24, ESRD, or RxHCC risk adjustment models. It can still be reported on Medicare Advantage encounter data submissions, but it does not contribute to the beneficiary's Risk Adjustment Factor (RAF) score and therefore does not affect the risk-adjusted capitation payment to the plan. V28 reached 100% phase-in for payment year 2026.

Question 3

Is Q87.88 billable?

Accepted Answer

Yes. Q87.88 is a billable ICD-10-CM code that can be reported on professional and institutional claims as a primary or secondary diagnosis when the provider documentation supports the specific condition described. Billable codes in ICD-10-CM are coded to the highest level of specificity available for the documented diagnosis. Q87.88 is current for fiscal year 2026 and remains in the active CMS ICD-10-CM code set published by the National Center for Health Statistics.

Question 4

What is the V28 vs V24 difference for Q87.88?

Accepted Answer

Q87.88 does not map to a payment HCC under either the CMS-HCC V28 risk adjustment model or the older V24 model. V28 reached 100% phase-in for payment year 2026, replacing V24 which was used during the PY2024–PY2025 transition. Because neither model rewards Q87.88 with a risk adjustment factor, it contributes zero to a Medicare Advantage beneficiary's RAF score in either version. Coders should check whether provider documentation supports a more specific child code that does map to a payment HCC.

Question 5

What should coders know when reporting Q87.88?

Accepted Answer

Verify genetic testing documentation supports CTNNB1 mutation diagnosis Code severity of developmental delay and intellectual disability with appropriate secondary codes

Q87.88

Is Q87.88 an HCC code?

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