QA0.013Neurodevelopmental disorders, related to pathogenic variants in other transporter and solute carrier genes

QA0.013 is the ICD-10-CM diagnosis code for neurodevelopmental disorders, related to pathogenic variants in other transporter and solute carrier genes. It belongs to category QA0 (neurodevelopmental disorders related to specific genetic pathogenic variants), block QA0-QA1 (genetic disorders, not elsewhere classified) and chapter 17 (congenital malformations, deformations, chromosomal abnormalities, and genetic disorders). It is a header code, so it can't be reported by itself; one of its 2 subcodes must be used instead.

Within QA0.01, choose QA0.013 (pathogenic variants in other transporter and solute carrier genes) only when documentation doesn't support a more specific option: pathogenic variants in ion channel genes (QA0.010), pathogenic variants in glutamate receptor genes (QA0.011), pathogenic variants in other receptor genes (QA0.012), pathogenic variants in synapse related genes (QA0.014) and genes associated with transcription and gene expression (QA0.015).

To report this condition, pick the subcode that matches the documentation: QA0.0131 (disorder) and QA0.0139 (gene).

It was added in FY2026, effective October 1, 2025.