ICD-10-CM 2026 · Effective October 1, 2025

ICD-10 QA0.0151

Billable / Specific

FOXG1 syndrome

QA0
Block
3
Synonyms
0
LCDs
0
Payer Policies
0
Linked CPTs

About ICD-10-CM QA0.0151

ICD-10-CM code QA0.0151 represents FOXG1 syndrome. This is a billable/specific code in the Congenital Malformations chapter (block QA0). The 2026 edition of ICD-10-CM QA0.0151 became effective on October 1, 2025.

Inclusion Terms / Approximate Synonyms

Clinical terms and conditions classified under QA0.0151. Per CMS ICD-10-CM Tabular 2026.

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

Medicare LCD Coverage for QA0.0151

Local Coverage Determinations (LCDs) from CMS MACs that list QA0.0151 as a covered diagnosis.

No Medicare LCDs reference QA0.0151 as covered

This doesn't mean the code isn't covered, it means no MAC has issued a Local Coverage Determination naming this specific code. Coverage may still apply under National Coverage Determinations or general medical-necessity rules.

Commercial Payer Coverage

Coverage policies from major commercial payers referencing QA0.0151.

No commercial payer policies reference QA0.0151 on file

Our payer policy database covers Aetna, Cigna, Anthem, BCBS, Humana, and Medicare Advantage plans, but QA0.0151 doesn't currently appear in any indexed policy. The code may still be covered under standard plan benefits.

CPT Codes Commonly Billed with QA0.0151

Procedures frequently paired with this diagnosis based on PayerReady's Dx↔Px linkage data.

No procedure linkages on file for QA0.0151

We don't have CPT pairings indexed for this specific code yet. Use the CPT search above to find common procedures, or check your payer's published medical policy for code-specific guidance.

Codes Adjacent To QA0.0151

Other codes in section QA0 (Genetic disorders, not elsewhere classified).

QA0 Neurodevelopmental disorders related to specific genetic pathogenic variants (non-billable) QA0.0 Neurodevelopmental disorders related to pathogenic variants in specific genes (non-billable) QA0.01 Neurodevelopmental disorders related to pathogenic variants in certain specific genes (non-billable) QA0.010 Neurodevelopmental disorders, related to pathogenic variants in ion channel genes (non-billable) QA0.0101 SCN2A-related neurodevelopmental disorder QA0.0102 CACNA1A-related neurodevelopmental disorder QA0.0109 Neurodevelopmental disorder related to pathogenic variant in other ion channel gene QA0.011 Neurodevelopmental disorders, related to pathogenic variants in glutamate receptor genes QA0.012 Neurodevelopmental disorders, related to pathogenic variants in other receptor genes QA0.013 Neurodevelopmental disorders, related to pathogenic variants in other transporter and solute carrier genes (non-billable) QA0.0131 SLC6A1-related disorder QA0.0139 Neurodevelopmental disorder, related to pathogenic variant in other transporter or solute carrier gene QA0.014 Neurodevelopmental disorders, related to pathogenic variants in synapse related genes (non-billable) QA0.0141 Syntaxin-binding protein 1-related disorder QA0.0142 DLG4-related synaptopathy QA0.0149 Neurodevelopmental disorder, related to pathogenic variant in other synapse related gene QA0.015 Neurodevelopmental disorders, related to genes associated with transcription and gene expression (non-billable) QA0.0159 Neurodevelopmental disorder, related to other genes associated with transcription and gene expression QA0.8 Other neurodevelopmental disorders related to pathogenic variants in other specific genes

ICD-10 QA0.0151, Billing FAQ

Is ICD-10 code QA0.0151 billable? +

Yes, QA0.0151 is a billable ICD-10-CM code that can appear as a primary or secondary diagnosis on claims.

What other names or terms map to QA0.0151? +

ICD-10 QA0.0151 includes: FOXG1-related disorder; FOXG1-related encephalopathy; FOXG1-related neurodevelopmental disorder.

Get the full PayerReady toolkit

Free access to CPT/ICD-10 lookup, denial appeals, fee comparator, and claim auditing with credentialing enrollment.

Start free →

Run this code through our claim audit tool

Check NCCI bundling, MUE limits, and modifier logic before submission.

Try the auditor →

Did this page help?

Quick signal so we know what to improve.

Thanks!

If you want a code reference page that doesn't exist yet, email coding@payerready.com.

Sorry to hear that.

Tell us what's missing or wrong: coding@payerready.com. We respond within 5 business days.

Reviewed by the PayerReady Medical Coding Team

Verified against the CMS 2026 code set on May 31, 2026.

Powered by 11K CPT · 98K ICD-10 · 860K MPFS rates · 4.5M NCCI edits · 9.5M NPIs. Our data methodology · About our coding team

Faster Approvals

Ready to Cut Your Enrollment Timeline in Half?

Join providers in all 50 states who handed off credentialing to a dedicated specialist. Create your free account in minutes and start enrolling the same day.

All 50 States Covered
No Long-Term Contracts
HIPAA HIPAA Compliant Platform
Dedicated Specialist Included