QA0.0151Billable
FOXG1 syndrome
- Chapter
- —
- Category
- QA0
- Effective date
- October 1, 2026
Related codes in category QA0
QA0Neurodev disord related to specific genetic patho variantsQA0.0Neurodev disord related to patho variants in specific genesQA0.01Neurodev disord rel to patho var in certain specific genesQA0.010Neurodev disord, related to patho var in ion channel genesQA0.0101SCN2A-related neurodevelopmental disorderYesQA0.0102CACNA1A-related neurodevelopmental disorderYesQA0.0109Neurodev disord rel to patho var in other ion channel geneYesQA0.011Neurodev disord, rel to patho var in glutamate recept genesYesQA0.012Neurodev disord, related to patho var in other recept genesYesQA0.013Neurodev dis, rel to patho var in oth trnsper /sol car genesQA0.0131SLC6A1-related disorderYesQA0.0139Neurodev dis,rel to patho var in oth trnsper or sol car geneYes
Frequently asked questions
What is ICD-10 code QA0.0151?
QA0.0151 is an ICD-10-CM diagnosis code for FOXG1 syndrome.
Is QA0.0151 a billable code?
Yes. QA0.0151 is billable and specific enough to be used on a claim.
When did QA0.0151 become effective?
QA0.0151 has been effective since October 1, 2026, per the CMS/CDC ICD-10-CM annual release.
What other codes are related to QA0.0151?
QA0.0151 belongs to category QA0, which includes 12 other codes — see the related codes list on this page.
ICD-10-CM data maintained by CDC/CMS (public domain). Always verify codes with authoritative sources before making coding or billing decisions.