QA0.0139: Neurodevelopmental disorder, related to pathogenic variant in other transporter or solute carrier gene
QA0.0139 is the billable ICD-10-CM diagnosis code for Neurodevelopmental disorder, related to pathogenic variant in other transporter or solute carrier gene. It is a fully specified code, so it can be reported on a claim (subject to clinical documentation and your payer's rules).
Frequently asked questions
What is ICD-10-CM code QA0.0139?
QA0.0139 is the ICD-10-CM diagnosis code for Neurodevelopmental disorder, related to pathogenic variant in other transporter or solute carrier gene. It belongs to category QA0 (Neurodevelopmental disorders related to specific genetic pathogenic variants).
Is QA0.0139 a billable code?
Yes. QA0.0139 is a billable, fully specified ICD-10-CM code, so it can be used on a claim (subject to documentation and payer rules).
What category does QA0.0139 belong to?
QA0.0139 is part of ICD-10-CM category QA0 — Neurodevelopmental disorders related to specific genetic pathogenic variants, which has 26 billable codes.
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Informational only, not coding or medical advice. Verify against the official ICD-10-CM (FY2026) and your payer's guidelines.
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