QA0.0139Billable
Neurodevelopmental disorder, related to pathogenic variant in other transporter or solute carrier gene
Short description: Neurodev dis,rel to patho var in oth trnsper or sol car gene
- Chapter
- —
- Category
- QA0
- Effective date
- October 1, 2026
Related codes in category QA0
QA0Neurodev disord related to specific genetic patho variantsQA0.0Neurodev disord related to patho variants in specific genesQA0.01Neurodev disord rel to patho var in certain specific genesQA0.010Neurodev disord, related to patho var in ion channel genesQA0.0101SCN2A-related neurodevelopmental disorderYesQA0.0102CACNA1A-related neurodevelopmental disorderYesQA0.0109Neurodev disord rel to patho var in other ion channel geneYesQA0.011Neurodev disord, rel to patho var in glutamate recept genesYesQA0.012Neurodev disord, related to patho var in other recept genesYesQA0.013Neurodev dis, rel to patho var in oth trnsper /sol car genesQA0.0131SLC6A1-related disorderYesQA0.014Neurodev disord, rel to patho var in synapse related genes
Frequently asked questions
What is ICD-10 code QA0.0139?
QA0.0139 is an ICD-10-CM diagnosis code for Neurodevelopmental disorder, related to pathogenic variant in other transporter or solute carrier gene.
Is QA0.0139 a billable code?
Yes. QA0.0139 is billable and specific enough to be used on a claim.
When did QA0.0139 become effective?
QA0.0139 has been effective since October 1, 2026, per the CMS/CDC ICD-10-CM annual release.
What other codes are related to QA0.0139?
QA0.0139 belongs to category QA0, which includes 12 other codes — see the related codes list on this page.
ICD-10-CM data maintained by CDC/CMS (public domain). Always verify codes with authoritative sources before making coding or billing decisions.