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.
Risk adjustment
QA0.012 does not map to an HCC and does not risk-adjust under CMS-HCC V28. That is normal — most ICD-10 codes do not. It still needs to be coded correctly; it just will not move a RAF score.
How QA0.012 is indexed
Coders do not find codes by browsing the tabular list — they look them up in the alphabetic index, under the word the physician wrote. These are the index entries that lead here, so you can see which chart wordings map to QA0.012.
- Disorder›neurodevelopmental›other›receptor gene related
Related codes at this level
Codes that share QA0.01. If QA0.012 is not quite right, the correct code is usually one of these.
- 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
Questions about QA0.012
- Is QA0.012 a billable ICD-10-CM code?
- Yes. QA0.012 is a billable, specific ICD-10-CM code and is valid for submission on a claim.
- Where does QA0.012 sit in the tabular list?
- Congenital malformations, deformations and chromosomal abnormalities (Q00-QA0), in the block Genetic disorders, not elsewhere classified (QA0).