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QA0.013 Neurodevelopmental disorders, related to pathogenic variants in other transporter and solute carrier genes

Not billable (header)Chapter 17

Report one of the more specific codes below.

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Codes under this one

QA0.0131 SLC6A1-related disorder
QA0.0139 Neurodevelopmental disorder, related to pathogenic variant in other transporter or solute carrier gene

Instructional notes

Chapter 17

Excludes2Not included here: the patient may have both; report both when both are present.

inborn errors of metabolism (E70-E88)

Notes

Codes from this chapter are not for use on maternal records

QA0

Code also

, if applicable, any associated conditions, such as:
attention-deficit hyperactivity disorders (F90.-)
autism spectrum disorder (F84.0)
developmental and epileptic encephalopathy (G93.45)
epilepsy, by specific type (G40.-)
intellectual disabilities (F70-F79)
pervasive developmental disorders (F84.-)

Chapter 17: Congenital malformations, deformations, chromosomal abnormalities, and genetic disorders (Q00-QA1) · QA0-QA1 Genetic disorders, not elsewhere classified (QA0-QA1)

Source: ICD-10-CM FY 2027 code descriptions and tabular list (CMS and CDC National Center for Health Statistics), effective 2026-10-01 through 2027-09-30 · CMS ICD-10 files. HCC mapping: CMS-HCC V28, payment year 2027. As of 2026-11-04.

Coverage and payment depend on the claim details; confirm with the Medicare Administrative Contractor.