QA1.79 Other inherited neoplasm predisposition syndrome of multiple systems
Not valid for submission — needs a 6th character ICD10CM Release FY2027
Valid codes under QA1.79
QA1.79 is a complete ICD-10-CM concept, but not valid for submission on its own — it needs a 6th character. The valid codes are:
- QA1.790 Familial cancer syndrome with pathogenic BRCA1 mutation
- QA1.791 Familial cancer syndrome with pathogenic BRCA2 mutation
- QA1.792 Li Fraumeni syndrome
- QA1.798 Other inherited neoplasm predisposition syndrome of multiple systems
Short description: Other inherited neoplm predisposition synd of mult systems
Version history
| Release | Valid from | Valid to | Description | Billable |
|---|---|---|---|---|
| FY2027 | 2026-10-01 | current | Other inherited neoplasm predisposition syndrome of multiple systems | no |
Related codes in QA1
- QA1 Genetic disorders associated with neoplasms, not elsewhere classified
- QA1.7 Inherited neoplasm predisposition syndromes involving multiple systems, not elsewhere classified
- QA1.71 Lynch syndrome
- QA1.790 Familial cancer syndrome with pathogenic BRCA1 mutation
- QA1.791 Familial cancer syndrome with pathogenic BRCA2 mutation
- QA1.792 Li Fraumeni syndrome