QA0.012
QA0.012: Neurodevelopmental disorders, related to pathogenic variants in other receptor genes
Billable / specific codeICD-10-CM
QA0.012 is a billable, specific ICD-10-CM code for neurodevelopmental disorders, related to pathogenic variants in other receptor genes. It is valid for submission on a claim.
Check QA0.012 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›other›receptor gene related
Code history
- addedFY2024-FY2027
Neurodevelopmental disorders, related to pathogenic variants in other receptor genes
Other codes under QA0.01
- QA0.010Neurodevelopmental disorders, related to pathogenic variants in ion channel genes
- QA0.011Neurodevelopmental disorders, related to pathogenic variants in glutamate 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