QA0.012

Neurodevelopmental disorders, related to pathogenic variants in other receptor genes

Billable / specificPOA exempt

QA0.012 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.

  • inborn errors of metabolism (E70-E88) (from QA0)

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, other, receptor gene 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
  • QA0.011Neurodevelopmental disorders, related to pathogenic variants in glutamate 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

Browse