QA0.01
Neurodevelopmental disorders related to pathogenic variants in certain specific genes
QA0.01 is a non-billable ICD-10-CM code header for neurodevelopmental disorders related to pathogenic variants in certain specific genes. Report a more specific code from it instead. It is part of the FY2027 code set, effective October 1, 2026. The more specific codes under it are QA0.010 Neurodevelopmental disorders, related to pathogenic variants in ion channel genes; QA0.011 Neurodevelopmental disorders, related to pathogenic variants in glutamate receptor genes; QA0.012 Neurodevelopmental disorders, related to pathogenic variants in other receptor genes; QA0.013 Neurodevelopmental disorders, related to pathogenic variants in other transporter and solute carrier genes and 2 more. Its coding notes include a Code also instruction and 1 Excludes2 entry.
Guidelines tip
From the FY2027 Official Guidelines. ICD10Ref adds no rules of its own.
Chapter 17 codes can be used for life. Manifestations that are an inherent part of a specifically coded anomaly are not coded separately. A corrected malformation is reported with a personal history code.
Code also
Two codes may be needed to describe the condition. This note gives no sequencing order.
Excludes2
Not included here. Both codes may be reported if the patient has both conditions.
Also from chapter/block level (1 note)
- inborn errors of metabolism (E70-E88)
Notes
Also from chapter/block level (1 note)
- Codes from this chapter are not for use on maternal records
More specific codes under QA0.01 6
- QA0.010Neurodevelopmental disorders, related to pathogenic variants in ion channel genesHeader
- QA0.011Neurodevelopmental disorders, related to pathogenic variants in glutamate receptor genesBillable
- QA0.012Neurodevelopmental disorders, related to pathogenic variants in other receptor genesBillable
- QA0.013Neurodevelopmental disorders, related to pathogenic variants in other transporter and solute carrier genesHeader
- QA0.014Neurodevelopmental disorders, related to pathogenic variants in synapse related genesHeader
- QA0.015Neurodevelopmental disorders, related to genes associated with transcription and gene expressionHeader