QA0.012BillableSave
QA0.012 - Neurodevelopmental disorders, related to pathogenic variants in other receptor genes
ICD-10-CM Chapter 17: Congenital malformations, deformations and chromosomal abnormalities · QA0-QA1 Genetic disorders, not elsewhere classified (QA0-QA1) · Subcategory of QA0.01 · FY2027
Includes, Excludes and Coding Notes
Code AlsoFrom QA0
Report an additional code when both conditions apply.
- , if applicable, any associated conditions, such as:
- attention-deficit hyperactivity disorders (F90.-)
- autism spectrum disorder (F84.0)
- developmental and epileptic encephalopathy (G93.45)
- epilepsy, by specific type (G40.-)
- intellectual disabilities (F70-F79)
- pervasive developmental disorders (F84.-)
Excludes 2 — Not Included HereFrom Chapter Q00-Q99
Not part of this code; report both codes when the patient has both conditions.
- inborn errors of metabolism (E70-E88)
NotesFrom Chapter Q00-Q99
Instructional notes from the ICD-10-CM tabular list.
- Codes from this chapter are not for use on maternal records
Chapter Information
Chapter 17: Congenital malformations, deformations and chromosomal abnormalities
Range: Q00-Q99
View full chapterOther codes in QA0.01
Codes at the same level as QA0.012
- Neurodevelopmental disorders, related to pathogenic variants in ion channel genesQA0.010
- Neurodevelopmental disorders, related to pathogenic variants in glutamate receptor genesQA0.011
- Neurodevelopmental disorders, related to pathogenic variants in other transporter and solute carrier genesQA0.013
- Neurodevelopmental disorders, related to pathogenic variants in synapse related genesQA0.014
- Neurodevelopmental disorders, related to genes associated with transcription and gene expressionQA0.015