Q87.88
CTNNB1 syndrome
- Release
- FY 2027
- Effective
Hierarchy
Where Q87.88 sits in the official hierarchy. Each level is the code it is classified under.
Official Coding Notes
Reproduced verbatim from the FY 2027 ICD-10-CM files. Notes labelled as inherited are declared on a parent code and apply here too.
Use Additional Code
code, if applicable, for associated conditions such as:
Use Additional Code
code(s) to identify all associated manifestations
Inherited from Q87 — Other specified congenital malformation syndromes affecting multiple systems
Use Additional Code
cerebral palsy ( G80 .-)
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congenital heart malformations (Q20.0-Q24.9)
Use Additional Code
developmental disorder of speech and language ( F80 .-)
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exudative retinopathy ( H35.02- )
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intellectual disability (F70-F79)
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microcephaly ( Q02 )
Version History
How Q87.88 appears in each release imported from the official files, newest first.
-
FY 2027 Effective
CurrentCTNNB1 syndrome
-
FY 2026 Effective
UnchangedCTNNB1 syndrome
Related Codes
Other codes under Q87.8
- Q87.81 Alport syndrome Billable
- Q87.82 Arterial tortuosity syndrome Billable
- Q87.83 Bardet-Biedl syndrome Billable
- Q87.84 Laurence-Moon syndrome Billable
- Q87.85 MED13L syndrome Billable
- Q87.86 Kleefstra syndrome Billable
- Q87.87 Hao-Fountain Syndrome Billable
- Q87.89 Other specified congenital malformation syndromes, not elsewhere classified Billable
Data Source
Code information on this page is derived from the FY 2027 ICD-10-CM files published by CDC NCHS and CMS.
- Release
- FY 2027
- Effective
- Source file
- icd10cm-code-descriptions-2027.zip
Official ICD-10-CM source files (opens in a new tab)
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