Is ICD-10-CM code QA0.0151 billable?

Yes, QA0.0151 (FOXG1 syndrome) is a billable ICD-10-CM diagnosis code, valid for reimbursement on HIPAA-covered transactions for FY2027.

Is QA0.0151 exempt from POA reporting?

Yes, QA0.0151 is on the CMS list of ICD-10-CM codes exempt from Present On Admission (POA) reporting for FY2027. Inpatient claims do not require a POA indicator for this code.

What chapter does ICD-10-CM code QA0.0151 belong to?

QA0.0151 belongs to Chapter 17 of the ICD-10-CM tabular list: Q00–Q99 (Congenital Malformations, Deformations and Chromosomal Abnormalities).

QA0.0151BillableCC No HCC POA Exempt

FOXG1 syndrome

Congenital Malformations, Deformations and Chromosomal Abnormalities·Neurodevelopmental disorders, related to genes associated with transcription and gene expression·subcategory·FY 2027

Also indexed as: Disorder, FOXG1-related; Disorder, neurodevelopmental, FOXG1-related; Encephalopathy, FOXG1-related; Syndrome, FOXG1

Instructional notes

Includes: conditions that are coded here

FOXG1-related disorder
FOXG1-related encephalopathy
FOXG1-related neurodevelopmental disorder

Also applies, from QA0: Neurodevelopmental disorders related to specific genetic pathogenic variants

These notes sit on QA0 and apply to every code under it, including QA0.0151.

Code also: add a code for this too, order depends on the encounter

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.-)

Where QA0.0151 sits

MS-DRGs

As the principal diagnosis, this code groups to these MS-DRGs (v44.0). Which one applies depends on procedures performed, secondary diagnoses (CC/MCC), and the patient's age and discharge status.

Code history

FY 2025: replaced F89 (Unspecified disorder of psychological development)