F78.A9 ICD-10-CM Code: Other genetic related intellectual disability
F78.A9 is not a CMS-HCC payment code. MEAT criteria · RAF Calculator · HCC coding software
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FY 2026 Apr update / Mental, Behavioral and Neurodevelopmental disorders (F01-F99) / Intellectual Disabilities (F70-F79)
F78.A9
Billable / SpecificICD-10-CMOfficial ICD-10-CMCodebook guidanceOther genetic related intellectual disability
Intellectual disability caused by genetic factors that don't fit into other specific genetic categories. This represents a significant limitation in intellectual functioning and adaptive behavior due to inherited genetic conditions.

Buddy Insight
This code captures intellectual disability with a confirmed genetic etiology that is not SYNGAP1 (which has its own code at F78.
CMS-HCC V28
N/A—
Not mapped
CMS-HCC V24
HistoricalHistorical
Not used for CY2026 payment
ACA/HHS
N/A—
Not mapped
ESRD/PACE
N/A—
Not mapped
RXHCC
MappedHCC 148
Code-level coefficient reference
Code Book Path
Inclusion Terms
OfficialNo inclusion terms are included in this display for F78.A9. Check the code and parent instructions in the Code Book.
Excludes 2
Official- symptoms, signs and abnormal clinical laboratory findings, not elsewhere classified (R00-R99)Inherited from F01-F99
Related Codes
Includes
Official- disorders of psychological developmentInherited from F01-F99
Excludes 1
Official- borderline intellectual functioning, IQ above 70 to 84 (R41.83)Inherited from F70-F79
Code First
Official- any associated physical or developmental disordersInherited from F70-F79
Use Additional
OfficialNo Use Additional Code instructions are included in this display for F78.A9. Check the code and parent instructions in the Code Book.
Code Also
Official- , if applicable, any associated disorders
Buddy Documentation Tip
MEAT Support
Audit Caution
Common Mistakes
Current with CMS: FY2026 ICD-10-CM Apr 1 update (effective Apr 1 – Sep 30, 2026) · CMS-HCC V28, 100% phased in for payment year 2026. FY2027 code set already staged for October 1, 2026. How HCC Buddy stays current →
Is F78.A9 an HCC code?
F78.A9 is not in the CMS-HCC V28 or V24 community payment model. F78.A9 has a separate mapping under the Part D RxHCC model (HCC 148 (Mild or Unspecified Intellectual Disability/Developmental Disorder)); the applicable result needs member context.
- Code
- F78.A9
- Description
- Other genetic related intellectual disability
- HCC (V28)
- No CMS-HCC V28 mapping
- RAF reference coefficient
- —
- Billable
- Yes
- Payment year
- 2026
HCC Category Mapping
These are source-labeled model coefficients, not member totals. A category may still be removed by hierarchy or model cleanup rules. Weights are not directly comparable across models: CMS-HCC V28 and V24 use Community, Non-Dual, Aged; ESRD uses the dialysis continuing-enrollee model; RxHCC is the Part D continuing-enrollee, non-low-income, aged weight (a larger scale than CMS-HCC). ACA/HHS has no single weight — it varies by metal level. Actual per-patient RAF contribution depends on member context, hierarchy and cleanup rules, interactions, and the model year used by the payer. V28 is the CMS-HCC model phased in over payment years 2024–2026; V24 remains available for historical review.
Work F78.A9 in the Code Book — tabular path, V28 RAF reference, and MEAT checklist →
MEAT review for F78.A9
For F78.A9, confirm that the documentation supports the diagnosis and meets the applicable coding, encounter, program and payer requirements. MEAT (Monitor, Evaluate, Assess, or Treat) is a review mnemonic, not a universal CMS coding rule.
- MMonitor: signs, symptoms, disease progression, or lab trending documented in the note
- EEvaluate: test results, medication response, or physical findings reviewed by the provider
- AAssess: explicit mention in the assessment or plan with acknowledgment of status
- TTreat: medication, referral, procedure, therapy, or counseling tied to the diagnosis
Coder workflow notes
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What This Code Means
F78.A9 is the ICD-10-CM diagnosis code for other genetic related intellectual disability. Intellectual disability caused by genetic factors that don't fit into other specific genetic categories. This represents a significant limitation in intellectual functioning and adaptive behavior due to inherited genetic conditions. F78.A9 sits in the ICD-10-CM chapter for mental, behavioral and neurodevelopmental disorders (f01-f99), within the section covering intellectual disabilities (f70-f79).
F78.A9 has no mapping under the CMS-HCC V28 or V24 community payment models. F78.A9 has a separate mapping under the Part D RxHCC model (HCC 148 (Mild or Unspecified Intellectual Disability/Developmental Disorder)); the applicable result needs member context. Do not assign V28 risk adjustment value from this page; verify the applicable model and payment year before using this code for risk adjustment.
Use this code only after ruling out other specific genetic intellectual disability codes (F78.A0-F78.A8).
HCC Buddy maintains structured V28 and V24 mapping, source-labeled coefficient references, and MEAT documentation criteria for F78.A9 sourced directly from the CMS-HCC risk adjustment model files and the CMS ICD-10-CM code set.
Coding Tips
- •Use this code only after ruling out other specific genetic intellectual disability codes (F78.A0-F78.A8)
- •Document the genetic condition or syndrome when possible to support medical necessity and potential future specificity
Clinical Significance
This code captures intellectual disability with a confirmed genetic etiology that is not SYNGAP1 (which has its own code at F78.A1). This includes intellectual disability caused by other single-gene mutations, chromosomal microdeletions/duplications, or other genetic conditions not elsewhere classified. Documenting the genetic basis supports research, family counseling, and targeted management approaches.
Documentation Requirements
- ✓Genetic testing results confirming a genetic cause of intellectual disability (other than SYNGAP1)
- ✓Provider documentation linking the intellectual disability to the identified genetic finding
- ✓Specification of the genetic condition if possible in the clinical notes
- ✓Documentation of intellectual disability severity and associated features
- ✓Genetic counseling documentation and family history assessment
Code Also
- , if applicable, any associated disorders
Commonly Confused Codes
- •F78.A1: SYNGAP1-related intellectual disability; use F78.A1 if the specific gene is SYNGAP1
- •Q90.x: Down syndrome; Down syndrome has its own specific codes and should not use F78.A9
- •Q87.x: Other specified congenital malformation syndromes; many genetic syndromes have specific codes
- •F79: Unspecified intellectual disabilities; use F78.A9 when genetic etiology is confirmed, not the unspecified code

