QA0.0151 FOXG1 syndrome
Billable / valid for submission ICD10CM Release FY2026
Version history
| Release | Valid from | Valid to | Description | Billable |
|---|---|---|---|---|
| FY2026 | 2025-10-01 | current | FOXG1 syndrome | yes |
Related codes in QA0
- QA0 Neurodevelopmental disorders related to specific genetic pathogenic variants
- QA0.0 Neurodevelopmental disorders related to pathogenic variants in specific genes
- QA0.01 Neurodevelopmental disorders related to pathogenic variants in certain specific genes
- QA0.010 Neurodevelopmental disorders, related to pathogenic variants in ion channel genes
- 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
- 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
- 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
- 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