QA0.0139
QA0.0139 — Neurodevelopmental disorder, related to pathogenic variant in other transporter or solute carrier gene
Billable / specific codeICD-10-CM
QA0.0139 is a billable, specific ICD-10-CM code for neurodevelopmental disorder, related to pathogenic variant in other transporter or solute carrier gene. It is valid for submission on a claim.
Risk adjustment
QA0.0139 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 QA0.0139 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 QA0.0139.
- Disorder›neurodevelopmental›other›transporter or solute carrier gene related
Related codes at this level
Codes that share QA0.013. If QA0.0139 is not quite right, the correct code is usually one of these.
Questions about QA0.0139
- Is QA0.0139 a billable ICD-10-CM code?
- Yes. QA0.0139 is a billable, specific ICD-10-CM code and is valid for submission on a claim.
- Where does QA0.0139 sit in the tabular list?
- Congenital malformations, deformations and chromosomal abnormalities (Q00-QA0), in the block Genetic disorders, not elsewhere classified (QA0).