Neurodevelopmental disorders, related to pathogenic variants in glutamate receptor genes
Billable / specificPOA exempt
QA0.011 is a billable, specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes in FY2027.
Inclusion terms
Includes (from QA0)
- Note: Codes from this chapter are not for use on maternal records
Excludes2
Not included here — may be reported together when both conditions exist.
Code also
An additional code may be needed.
- , if applicable, any associated conditions, such as: (from QA0)
- attention-deficit hyperactivity disorders (F90.-) (from QA0)
- autism spectrum disorder (F84.0) (from QA0)
- developmental and epileptic encephalopathy (G93.45) (from QA0)
- epilepsy, by specific type (G40.-) (from QA0)
- intellectual disabilities (F70-F79) (from QA0)
- pervasive developmental disorders (F84.-) (from QA0)
Also known as
- Disorder, neurodevelopmental, GRIN1-related
- Disorder, neurodevelopmental, GRIN2A-related
- Disorder, neurodevelopmental, GRIN2B-related
- Disorder, neurodevelopmental, GRIN2D-related
- Disorder, neurodevelopmental, GRIA1-related
- Disorder, neurodevelopmental, GRIA2-related
- Disorder, neurodevelopmental, GRIA3-related
- Disorder, neurodevelopmental, GRIA4-related
- Disorder, neurodevelopmental, GRIK2-related
- Disorder, neurodevelopmental, other, glutamate receptor, ionotropic, related
Parent code
- QA0.01Neurodevelopmental disorders related to pathogenic variants in certain specific genesHeader
Related codes
- QA0.010Neurodevelopmental disorders, related to pathogenic variants in ion channel genesHeader
- 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