QA1.791
Familial cancer syndrome with pathogenic BRCA2 mutation
- Release
- FY 2027
- Effective
Hierarchy
Where QA1.791 sits in the official hierarchy. Each level is the code it is classified under.
- QA1 Genetic disorders associated with neoplasms, not elsewhere classified
- QA1.7 Inherited neoplasm predisposition syndromes involving multiple systems, not elsewhere classified
- QA1.79 Parent Other inherited neoplasm predisposition syndrome of multiple systems
- QA1.791 This code Familial cancer syndrome with pathogenic BRCA2 mutation
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.
Inclusion Terms
BRCA2-cancer predisposition syndrome
Inclusion Terms
Hereditary breast and ovarian cancer syndrome with pathogenic BRCA2 mutation
Code Also
, if applicable, any associated conditions, such as:
Inherited from QA1 — Genetic disorders associated with neoplasms, not elsewhere classified
Code Also
genetic susceptibility to malignant neoplasm by site ( Z15.0- )
Inherited from QA1 — Genetic disorders associated with neoplasms, not elsewhere classified
Code Also
malignant neoplasms (C00.0-C96.9)
Inherited from QA1 — Genetic disorders associated with neoplasms, not elsewhere classified
Version History
How QA1.791 appears in each release imported from the official files, newest first.
-
FY 2027 Effective
NewFamilial cancer syndrome with pathogenic BRCA2 mutation
Related Codes
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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