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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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Code lookupF78.A9

FY 2026 Apr update / Mental, Behavioral and Neurodevelopmental disorders (F01-F99) / Intellectual Disabilities (F70-F79)

F78.A9

Billable / SpecificICD-10-CMOfficial ICD-10-CMCodebook guidance

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.

Buddy the Bee presenting code insight

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

Historical

Historical

Not used for CY2026 payment

ACA/HHS

N/A

Not mapped

ESRD/PACE

N/A

Not mapped

RXHCC

HCC 148

Code-level coefficient reference

Inclusion Terms

Official

No 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

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

Official

No 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

HCC Buddy guidance
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

MEAT Support

HCC Buddy guidance
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

Audit Caution

HCC Buddy guidance
Using F78.A9 when the genetic condition has its own specific ICD-10-CM code (Down syndrome, Fragile X, etc.)
Failing to also code the specific genetic syndrome when one exists alongside the intellectual disability code
Using unspecified intellectual disability (F79) when genetic testing has confirmed a genetic cause
Not updating coding when genetic test results return after an initial encounter

Common Mistakes

HCC Buddy guidance
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

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

RxHCCHCC 148, Mild or Unspecified Intellectual Disability/Developmental Disorder
Not separately weighted

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

Child Codes

Code Hierarchy

F78.A9 code history

Code setChange
FY2022 (effective Oct 1, 2021)Added to the code set

Source: official CMS ICD-10-CM order and addenda files, FY2016 through FY2027.

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