QA1.79 ICD-10-CM Code: Other inherited neoplasm predisposition syndrome of multiple systems
A clear reference for the official code description, hierarchy, and related coding information from the FY 2027 U.S. release.
Code definition
Official description
QA1.79Other inherited neoplasm predisposition syndrome of multiple systems
ICD-10-CM diagnosis code · United States clinical modification
Classification
Where QA1.79 sits
- 1
Chapter 17
Congenital malformations, deformations, chromosomal abnormalities, and genetic disorders (Q00-QA1)
- 2
Section
Genetic disorders, not elsewhere classified (QA0-QA1)
- 3
Category QA1
Genetic disorders associated with neoplasms, not elsewhere classified
- 4
Subcategory QA1.7
Inherited neoplasm predisposition syndromes involving multiple systems, not elsewhere classified
- 5
Code QA1.79
Other inherited neoplasm predisposition syndrome of multiple systems
More specific choices
Codes under QA1.79
QA1.79 is a non-billable category. Choose the child code that best matches the documented diagnosis.
Documentation details
Notes for this code
Inclusion terms
No inclusion terms are listed for QA1.79.
Code first
No “code first” instruction is listed for QA1.79.
Use additional code
No “use additional code” instruction is listed for QA1.79.
Excludes1
Conditions that should not be reported together with this code.
No Excludes1 note is listed for QA1.79.
Excludes2
Conditions not included here that may be reported separately when present.
No Excludes2 note is listed for QA1.79.
Transparency
Source and release
This reference is generated from Vero’s ICD-10-CM description, hierarchy, and code-note dataset. The visible content and structured data share that source.
Review the CDC/NCHS ICD-10-CM sourceCode-specific guidance
Frequently asked questions
What does ICD-10-CM code QA1.79 mean?
QA1.79 is the FY 2027 U.S. ICD-10-CM code for “Other inherited neoplasm predisposition syndrome of multiple systems.”
Is QA1.79 a billable or specific ICD-10-CM code?
No. QA1.79 has more specific child codes in the FY 2027 reference data. Select the code that matches the documentation and confirm the active code set and payer requirements.
Where is QA1.79 located in ICD-10-CM?
QA1.79 is listed in Chapter 17, Congenital malformations, deformations, chromosomal abnormalities, and genetic disorders (Q00-QA1), within Genetic disorders, not elsewhere classified (QA0-QA1) (QA0–QA1), under category QA1, Genetic disorders associated with neoplasms, not elsewhere classified and subcategory QA1.7, Inherited neoplasm predisposition syndromes involving multiple systems, not elsewhere classified.
What coding notes are listed for QA1.79?
No inclusion terms are listed for QA1.79 in this reference record. No code-first instruction is listed. No Excludes1 note is listed. No Excludes2 note is listed.
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