QA0.011
QA0.011: Neurodevelopmental disorders, related to pathogenic variants in glutamate receptor genes
Billable / specific codeICD-10-CM
QA0.011 is a billable, specific ICD-10-CM code for neurodevelopmental disorders, related to pathogenic variants in glutamate receptor genes. It is valid for submission on a claim.
Check QA0.011 with the rest of the claim: free scrubberRisk adjustment
No CMS-HCC V28 category: this code does not change a RAF score.
Alphabetic index entries that lead here
- Disorder›neurodevelopmental›GRIA1-related
- Disorder›neurodevelopmental›GRIA2-related
- Disorder›neurodevelopmental›GRIA3-related
- Disorder›neurodevelopmental›GRIA4-related
- Disorder›neurodevelopmental›GRIK2-related
- Disorder›neurodevelopmental›GRIN1-related
- Disorder›neurodevelopmental›GRIN2A-related
- Disorder›neurodevelopmental›GRIN2B-related
- Disorder›neurodevelopmental›GRIN2D-related
- Disorder›neurodevelopmental›other›glutamate receptor, ionotropic, related
Code history
- addedFY2024-FY2027
Neurodevelopmental disorders, related to pathogenic variants in glutamate receptor genes
Other codes under QA0.01
- QA0.010Neurodevelopmental disorders, related to pathogenic variants in ion channel genes
- QA0.012Neurodevelopmental disorders, related to pathogenic variants in other receptor genes
- QA0.013Neurodevelopmental disorders, related to pathogenic variants in other transporter and solute carrier genes
- QA0.014Neurodevelopmental disorders, related to pathogenic variants in synapse related genes
- QA0.015Neurodevelopmental disorders, related to genes associated with transcription and gene expression