Category · FY2027
F78 Other intellectual disabilities
- Header · not billable
F78 is not billable. The category heads 2 billable codes in FY2027, grouped under 1 subdivision.
Index → code
Where it sits
- Chapter 5 Mental, Behavioral and Neurodevelopmental disorders (F01-F99)
- F70-F79 Intellectual Disabilities (F70-F79)
- F78 Other intellectual disabilities
- Billable codes
- 2
- Subdivisions
- 1
- CC / MCC codes
- 0 / 0
- HCC V28 codes
- 0
- New FY2027
- 0
- Index entries
- 26
Codes in F78
- F78.AOther genetic related intellectual disabilitiesHeader
- F78.A1SYNGAP1-related intellectual disabilityBillable
- F78.A9Other genetic related intellectual disabilityBillable
Code also 1
Code also
- , if applicable, any associated disorders
Instructions
Notes that also apply
Block F70-F79 instructions (Excludes1 1, Code first 1): printed on the block page.
Chapter 5 instructions (Includes 1, Excludes2 1): printed on the chapter 5 page.
Index entries
- Disability, disabilities›intellectual›SYNGAP1-related → F78.A1
- Disability, disabilities›intellectual›autosomal dominant → F78.A9
- Disability, disabilities›intellectual›autosomal recessive → F78.A9
- Disability, disabilities›intellectual›genetic related → F78.A9
- Disability, disabilities›intellectual›specified level NEC → F78.A9
- Disability, disabilities›intellectual›X-linked (syndromic) (Bain type) → F78.A9
- Disability, disabilities›intellectual›with›pathogenic SYNGAP1 (genetic) (variant) → F78.A1
- Disability, disabilities›intellectual›genetic related›SYNGAP1-related → F78.A1
- Disability, disabilities›intellectual›with›pathogenic CHAMP1 (genetic) (variant) → F78.A9
- Disability, disabilities›intellectual›with›pathogenic HNRNPH2 (genetic) (variant) → F78.A9
- Disability, disabilities›intellectual›with›pathogenic SATB2 (genetic) (variant) → F78.A9
- Disability, disabilities›intellectual›with›pathogenic SETBP1 (genetic) (variant) → F78.A9
- Disability, disabilities›intellectual›with›pathogenic STXBP1 (genetic) (variant) → F78.A9
- Disability, disabilities›intellectual›genetic related›specified NEC → F78.A9
- Disability, disabilities›intellectual›in›autosomal dominant mental retardation → F78.A9
- Disability, disabilities›intellectual›in›autosomal recessive mental retardation → F78.A9
- Disability, disabilities›intellectual›in›SATB2-associated syndrome → F78.A9
- Disability, disabilities›intellectual›in›SETBP1 disorder → F78.A9
- Disability, disabilities›intellectual›in›STXBP1 encephalopathy with epilepsy → F78.A9
- Disability, disabilities›intellectual›in›X-linked mental retardation (syndromic) (Bain type) → F78.A9
- Disability, disabilities›intellectual›genetic related›with›pathogenic SYNGAP1 (variant) → F78.A1
- Disability, disabilities›intellectual›genetic related›with›pathogenic CHAMP1 (variant) → F78.A9
- Disability, disabilities›intellectual›genetic related›with›pathogenic HNRNPH2 (variant) → F78.A9
- Disability, disabilities›intellectual›genetic related›with›pathogenic SATB2 (variant) → F78.A9
- Disability, disabilities›intellectual›genetic related›with›pathogenic SETBP1 (variant) → F78.A9
- Disability, disabilities›intellectual›genetic related›with›pathogenic STXBP1 (variant) → F78.A9
NCHS Alphabetic Index. Index first, then the Tabular List.