QA1.792 ICD-10-CM Code: Li Fraumeni syndrome
Compare with another code for QA1.792Check this code on a claim
Billing Status: YES. This is a valid, specific, and billable ICD-10-CM reference.
Coding at a Glance
- Tabular directives
- 1 Excludes2 · 4 code-also instructions
Billable · FY2027A valid, specific ICD-10-CM code, reportable for dates of service in FY2027.
What you need to know
Source: CMS/NCHS Official ICD-10-CM tabular notes, quoted. From the CMS/NCHS tabular list for the release in force. A note the category or block publishes applies to this code too; the Instructions section marks which is which.
- Code alsoMay be needed with this code
- Excludes2Not included here; may be reported together
- multiple endocrine neoplasia [MEN] syndromes (E31.2-)
Where it sits Source: CMS/NCHS
Under:Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (Q00-QA1) (Q00-QA1)QA0-QA1 Genetic disorders, not elsewhere classified (QA0-QA1)QA1 Genetic disorders associated with neoplasms, not elsewhere classifiedQA1.7 Inherited neoplasm predisposition syndromes involving multiple systems, not elsewhere classifiedQA1.79 Other inherited neoplasm predisposition syndrome of multiple systems
Most relevant related codes MedCoder-derived
Read off the official notes above and this code’s own position in the tabular list. Which to report is a documentation question; Compare shows the two side by side.
Inpatient Payment Groups (MS-DRG)
Potential MS-DRG participation — not a DRG assignment.
MS-DRGs this diagnosis helps define, as principal or secondary, per the CMS ICD-10-CM/PCS MS-DRG Definitions Manual v44, Appendix B.
- MS-DRG 951 — OTHER FACTORS INFLUENCING HEALTH STATUS (MDC 23)
A diagnosis appearing in a group's logic does not by itself determine the DRG assigned to a stay; the grouper uses the full claim.
Coding instructions
Official Tabular Instructional Notes: the inclusion, exclusion and sequencing notes published for QA1.792 in the official ICD-10-CM tabular list, quoted as published.
Source: CMS/CDC — ICD-10-CM Tabular ListRelease: FY2027Effective: October 1, 2026
Trace:FY2027 changesChange historyRelease, file and checksum
Notes without a marker are published on QA1.792 itself; “inherited from” names the category or block whose note applies here.
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 QA1.792 vs E31.2 →
Source: inherited from QA1
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.-)
Source: inherited from QA1
Coder workflow for QA1.792
MedCoder structured workflow — derived from this code’s own official record
Documentation check
- The provider’s diagnostic statement
- Codes are assigned from the provider’s documented diagnosis, not from clinical criteria, test values or a medication list (Guidelines I.A.19).
- The associated condition or complication
- Whether the associated condition the title names is documented; the “with” convention presumes some links, and a provider statement that the conditions are unrelated defeats it (Guidelines I.A.15).
Official instructions as workflow
Excludes2 — not part of QA1.792(1 note)
Coding workflow: The conditions named in this note are not included in QA1.792. When the record documents both, both may be reported; the note is a boundary, not a prohibition.
CompareE31.2
See the official tabular notes · Guidelines I.A.12.b
Code Also — related condition(4 notes)
Coding workflow: Review the related condition when both are documented and the instruction applies. A Code Also note does not fix sequencing; the order follows the circumstances of the encounter.
See the official tabular notes · Guidelines I.A.17
Every row is derived from this code’s own record — its title, tabular notes, 7th-character family and same-category siblings — with fixed MedCoder wording; nothing is inferred about a patient. The official notes and guideline text are in the sections each row links to, and they control.
Coding context
Guidelines, coding notes, decision aids, relationships (with MS-DRG and CCSR classification), hierarchy, HCC, coverage and the context map: what a coder reaches for after the core. Each section names whether it is official source data, a MedCoder-derived relationship or MedCoder editorial.
Code Overview
MedCoder summary Summary composed by MedCoder from this code's official ICD-10-CM record. The tabular instructional notes themselves appear verbatim below.
Verify Before Coding
- No Medicare Code Editor or MS-DRG Definitions Manual restrictions apply to this code.
From the code registry, the Medicare Code Editor, and the MS-DRG Definitions Manual. Check it against a full claim in Claim Check.
Relationships & Classification
MedCoder-derived relationships — computed from published CMS and AHRQ datasets
MS-DRG Grouper Relationships (FY2027)
Potential MS-DRG participation — not a DRG assignment.
FY2027 MS-DRG: not on the CMS CC/MCC list — as a secondary diagnosis this code does not change MS-DRG severity for that release.
Named in the grouper logic of 1 MS-DRG: DRG 951 (MDC 23).
From the CMS MS-DRG Definitions Manual (Appendices B and C). Actual DRG assignment depends on the complete claim.
Contextual Map
Every relationship of QA1.792 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-QA1 — Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (Q00-QA1) (Q00-QA1)[Hierarchy]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- QA0-QA1 — Genetic disorders, not elsewhere classified[Hierarchy]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
MS-DRG Grouper
- DRG 951 — OTHER FACTORS INFLUENCING HEALTH STATUS[MS-DRG]: “OTHER FACTORS INFLUENCING HEALTH STATUS (MDC 23)”— CMS MS-DRG Definitions Manual (Appendix B) · FY2027
MDC crossing
- MDC 23 — Factors Influencing Health Status and Other Contacts with Health Services[MDC crossing]: “Factors Influencing Health Status and Other Contacts with Health Services — the grouper's crossing between diagnoses and procedures: a principal diagnosis sets the MDC, and same-MDC procedures move the stay to its surgical DRGs. 1,258 same-MDC procedures group here; browse them on the MDC page.”— CMS MS-DRG Definitions Manual · FY2027
Index entries
- Syndrome, Li-Fraumeni[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2027
Nearest codes
- QA1 — Genetic disorders associated with neoplasms, not elsewhere classified[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- QA1.7 — Inherited neoplasm predisposition syndromes involving multiple systems, not elsewhere classified[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- QA1.71 — Lynch syndrome[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- QA1.79 — Other inherited neoplasm predisposition syndrome of multiple systems[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- QA1.790 — Familial cancer syndrome with pathogenic BRCA1 mutation[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- QA1.791 — Familial cancer syndrome with pathogenic BRCA2 mutation[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- QA1.798 — Other inherited neoplasm predisposition syndrome of multiple systems[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
Change history
- FY2027 — Added to the code set[Change history]— CMS release files (code change ledger) · icd10cm-fy2027
Reference
Index terms and tables, published questions and FAQ, every source behind this page with its release and checksum, the date-of-service check and the complete change history.
Indexed Clinical Terms (1)
Official source data — entries quoted as published, in the Index’s own lookup phrasing
Clinical term phrases from the official ICD-10-CM Index to Diseases and Injuries that map to this code. These are alphabetic-index entries shown as the Index writes them — lookup phrasing, not necessarily the wording of a final diagnosis.
Sources for this page
Codes, titles, notes, index terms and mappings on this page are transcribed from the datasets below. Relationships MedCoder computed and text MedCoder wrote are labelled where they appear.
- Code, title, tabular notes and index terms Official source data
- CMS/CDC ICD-10-CM FY2027 tabular list, index and tables, effective October 1, 2026 Release, file and checksum · Publisher’s page
- Claim edits Official source data
- CMS Definitions of Medicare Code Edits — v44.0 (October 2026) Release, file and checksum · Publisher’s page
- Inpatient payment groups Official source data
- CMS MS-DRG Definitions Manual (incl. Appendix B diagnosis index, Appendix C CC/MCC list, Appendix E procedure index) and IPPS Final Rule tables — v44 Release, file and checksum · Publisher’s page
- Change history and date-of-service validity Official source data
- CMS ICD-10-CM release addenda, ingested release by release into the change ledger Release, file and checksum · Publisher’s page
- Comparisons, relationships and the contextual map MedCoder-derived relationship
- Computed by MedCoder from the tabular notes and tables above; every derived relationship is marked as derived where it appears
- Summary and FAQ answers MedCoder editorial explanation
- Written by MedCoder to explain the sources above: drafted with AI assistance, checked by a person against the release files, and labelled as MedCoder text where it appears. Not official text.
Current data releases:ICD-10-CM FY2027 · ICD-10-PCS FY2027 · HCPCS October 2026 · MS-DRG v44 · Medicare Code Editor v44.0 · NCCI PTP Q4 2026 · MUE Q4 2026 · NCD code lists 2026-01 · LCD export September 28, 2026 · All releases and sources
Labels on this page: Official source data · MedCoder-derived relationship · MedCoder editorial explanation. How to read the labels · All data sources and release dates · CMS coding rules
Cite this page
Reference this page in a research guide, syllabus or article. The release is included because code content changes each year.
MedCoder.ai. "QA1.792 — Li Fraumeni syndrome." ICD-10-CM FY2027. https://medcoder.ai/icd10/code/qa1.792-li-fraumeni-syndrome
Change history
Changed in FY2027, the release in force: Added to the code set.
- FY2027 — October 1, 2026Added to the code setLi Fraumeni syndromeFY2027 changes
Nearest Codes in This Family
Official ICD-10-CM classifications closest to QA1.792 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
- QA1.79 — Other inherited neoplasm predisposition syndrome of multiple systems
- QA1.790 — Familial cancer syndrome with pathogenic BRCA1 mutation
- QA1.791 — Familial cancer syndrome with pathogenic BRCA2 mutation
- QA1.798 — Other inherited neoplasm predisposition syndrome of multiple systems