ICD-10-CM Section · QA0-QA0

Genetic disorders, not elsewhere classified

20 codes in this section

20
Total Codes
13
Billable
7
Header (Non-Billable)
1
Top-Level Codes

About Section QA0

Section QA0 (QA0-QA0) covers genetic disorders, not elsewhere classified. It sits within the Congenital malformations, deformations, chromosomal abnormalities, and genetic disorders chapter (Q00-QA0). This section contains 20 ICD-10-CM codes, 13 billable diagnoses you can submit on a claim, and 7 non-billable header codes used to organize the hierarchy.

Codes are organized below by 3-character root. Click the root to see all subcodes underneath it, or click any individual code for full coverage data, payer policies, and linked CPT procedures.

Codes in QA0

Grouped by 3-character root code. Click any code for full detail.

QA0 Neurodevelopmental disorders related to specific genetic pathogenic variants
19 subcodes
QA0.0 Neurodevelopmental disorders related to pathogenic variants in specific genes Header
QA0.01 Neurodevelopmental disorders related to pathogenic variants in certain specific genes Header
QA0.010 Neurodevelopmental disorders, related to pathogenic variants in ion channel genes Header
QA0.0101 SCN2A-related neurodevelopmental disorder Billable
QA0.0102 CACNA1A-related neurodevelopmental disorder Billable
QA0.0109 Neurodevelopmental disorder related to pathogenic variant in other ion channel gene Billable
QA0.011 Neurodevelopmental disorders, related to pathogenic variants in glutamate receptor genes Billable
QA0.012 Neurodevelopmental disorders, related to pathogenic variants in other receptor genes Billable
QA0.013 Neurodevelopmental disorders, related to pathogenic variants in other transporter and solute carrier genes Header
QA0.0131 SLC6A1-related disorder Billable
QA0.0139 Neurodevelopmental disorder, related to pathogenic variant in other transporter or solute carrier gene Billable
QA0.014 Neurodevelopmental disorders, related to pathogenic variants in synapse related genes Header
QA0.0141 Syntaxin-binding protein 1-related disorder Billable
QA0.0142 DLG4-related synaptopathy Billable
QA0.0149 Neurodevelopmental disorder, related to pathogenic variant in other synapse related gene Billable
QA0.015 Neurodevelopmental disorders, related to genes associated with transcription and gene expression Header
QA0.0151 FOXG1 syndrome Billable
QA0.0159 Neurodevelopmental disorder, related to other genes associated with transcription and gene expression Billable
QA0.8 Other neurodevelopmental disorders related to pathogenic variants in other specific genes Billable

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Reviewed by the PayerReady Medical Coding Team

Verified against the CMS 2026 code set on May 31, 2026.

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