FOXG1 syndrome
Billable / specificPOA exempt
QA0.0151 is a billable, specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes in FY2027.
Inclusion terms
Applicable to
- FOXG1-related disorder
- FOXG1-related encephalopathy
- FOXG1-related neurodevelopmental disorder
Includes (from QA0)
- Note: Codes from this chapter are not for use on maternal records
Excludes2
Not included here — may be reported together when both conditions exist.
Code also
An additional code may be needed.
- , if applicable, any associated conditions, such as: (from QA0)
- attention-deficit hyperactivity disorders (F90.-) (from QA0)
- autism spectrum disorder (F84.0) (from QA0)
- developmental and epileptic encephalopathy (G93.45) (from QA0)
- epilepsy, by specific type (G40.-) (from QA0)
- intellectual disabilities (F70-F79) (from QA0)
- pervasive developmental disorders (F84.-) (from QA0)
Also known as
- FOXG1-related disorder
- FOXG1-related encephalopathy
- FOXG1-related neurodevelopmental disorder
- Disorder, FOXG1-related
- Disorder, neurodevelopmental, FOXG1-related
- Encephalopathy, FOXG1-related
- Syndrome, FOXG1
Parent code
- QA0.015Neurodevelopmental disorders, related to genes associated with transcription and gene expressionHeader
Related codes
- QA0.0159Neurodevelopmental disorder, related to other genes associated with transcription and gene expressionBillable