QA1.79 ICD-10-CM Code: Other inherited neoplasm predisposition syndrome of multiple systems
Billing Status: NO. This is a clinician non-billable / parent hierarchy grouping in the ICD-10-CM system.
Code Set: New for FY2027 — not valid before October 1, 2026.
Official Registry Overview & Definition
Official Tabular Instructional Notes
Sequencing, inclusion, and exclusion notes published for QA1.79 in the official ICD-10-CM tabular list.
Excludes2 — Not Included Here
Conditions not covered by this code, but which may be reported alongside it when both are present.
- multiple endocrine neoplasia [MEN] syndromes (E31.2-) Compare QA1.79 vs E31.2 →
Code Also
Additional codes that may be required to fully describe the encounter.
- Code also, if applicable, any associated conditions, such as:
- genetic susceptibility to malignant neoplasm by site (Z15.0-)
- malignant neoplasms (C00.0-C96.9)
- personal history of malignant neoplasm (Z85.-)
Change history
- FY2027 — 2026-10-01Added to the code setOther inherited neoplasm predisposition syndrome of multiple systemsFY2027 changes
Verify Before Coding
From the code registry, the Medicare Code Editor, and the MS-DRG Definitions Manual. Check it against a full claim.
Contextual Map
Every relationship of QA1.79 in one view: hierarchy, official tabular instructions in both directions, clinical classification, risk adjustment, MS-DRG participation, index terms and change history — each edge carrying the CMS source it derives from.
Hierarchy
- Q00-Q99 — Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (Q00-Q99) (Q00-Q99) [Hierarchy]
- QA1 — Clinical Diagnosis (QA1) [Hierarchy]
- QA1.7 — Clinical Diagnosis (QA1.7) [Hierarchy]
Nearest codes
- QA1 — Genetic disorders associated with neoplasms, not elsewhere classified [Sibling]
- QA1.7 — Inherited neoplasm predisposition syndromes involving multiple systems, not elsewhere classified [Sibling]
- QA1.71 — Lynch syndrome [Sibling]
- QA1.790 — Familial cancer syndrome with pathogenic BRCA1 mutation [Sibling]
- QA1.791 — Familial cancer syndrome with pathogenic BRCA2 mutation [Sibling]
- QA1.792 — Li Fraumeni syndrome [Sibling]
- QA1.798 — Other inherited neoplasm predisposition syndrome of multiple systems [Sibling]
Change history
- FY2027 — Added to the code set [Change history]
Frequently Asked Questions (FAQ) & Clinical Guidance
Can QA1.79 be billed directly?
No. QA1.79 (Other inherited neoplasm predisposition syndrome of multiple systems) is a non-billable ICD-10-CM category code. A more specific billable subcode must be selected based on clinical documentation.
Nearest Codes in This Family
Official ICD-10-CM classifications closest to QA1.79 in its code family, with their registry titles.
- 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
- QA1.798 — Other inherited neoplasm predisposition syndrome of multiple systems