QA0.0139
Billable
ChapterQ00–Q99
Ranksubcategory
Official Description
Neurodevelopmental disorder, related to pathogenic variant in other transporter or solute carrier gene
Metadata & Insights
- •2026 ICD-10-CM Edition - Effective October 1, 2025.
- •Billable/specific code (valid for reimbursement).
- •Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (Q00-Q99).
General instructions are available for the parent sections:
Clinical Hierarchy
CH17Congenital malformations, deformations and chromosomal abnormalities (Q00-QA0)
QA0Neurodevelopmental disorders related to specific genetic pathogenic variants
QA0.0Neurodevelopmental disorders related to pathogenic variants in specific genes
QA0.01Neurodevelopmental disorders related to pathogenic variants in certain specific genes
QA0.013Neurodevelopmental disorders, related to pathogenic variants in other transporter and solute carrier genes
QA0.0139Neurodevelopmental disorder, related to pathogenic variant in other transporter or solute carrier gene
Applicable Ancestor Context
The following parent sections contain instructions or notes that apply to QA0.0139:
categoryQA0
Neurodevelopmental disorders related to specific genetic pathogenic variants
View context instructionschapterCH17
Congenital malformations, deformations and chromosomal abnormalities (Q00-QA0)
View context instructionsAlphabetic Index Mentions
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1 raw paths
MS-DRG Classification
This code is grouped within the following Diagnosis Related Group(s) for clinical reimbursement:
Cross Reference
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