QA0 Neurodev disord related to specific genetic patho variants
ICD-10-CM category QA0 sits in Chapter 17 (Congenital malformations, deformations and chromosomal abnormalities, Q00-Q99). It contains 13 billable codes for FY2027, effective October 1, 2026 to September 30, 2027. Always code to the most specific code available: a code with more characters that describes the diagnosis more precisely takes priority over a shorter one.
Subcategories
QA0.0 Neurodev disord related to patho variants in specific genesQA0.01 Neurodev disord rel to patho var in certain specific genesQA0.010 Neurodev disord, related to patho var in ion channel genesQA0.013 Neurodev dis, rel to patho var in oth trnsper /sol car genesQA0.014 Neurodev disord, rel to patho var in synapse related genesQA0.015 Neurodev dis, rel to genes assoc w txn and gene expression
Billable codes in QA0
| Code | Description |
|---|---|
QA0.0101 | SCN2A-related neurodevelopmental disorder |
QA0.0102 | CACNA1A-related neurodevelopmental disorder |
QA0.0109 | Neurodevelopmental disorder related to pathogenic variant in other ion channel gene |
QA0.011 | Neurodevelopmental disorders, related to pathogenic variants in glutamate receptor genes |
QA0.012 | Neurodevelopmental disorders, related to pathogenic variants in other receptor genes |
QA0.0131 | SLC6A1-related disorder |
QA0.0139 | Neurodevelopmental disorder, related to pathogenic variant in other transporter or solute carrier gene |
QA0.0141 | Syntaxin-binding protein 1-related disorder |
QA0.0142 | DLG4-related synaptopathy |
QA0.0149 | Neurodevelopmental disorder, related to pathogenic variant in other synapse related gene |
QA0.0151 | FOXG1 syndrome |
QA0.0159 | Neurodevelopmental disorder, related to other genes associated with transcription and gene expression |
QA0.8 | Other neurodevelopmental disorders related to pathogenic variants in other specific genes |
Search within ICD-10-CM for QA0 and related codes