QA0.0142

DLG4-related synaptopathy

Billable / specificPOA exempt

QA0.0142 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, DLG4-related synaptopathy
  • Synaptopathy, DLG4-related

Parent code

  • QA0.014Neurodevelopmental disorders, related to pathogenic variants in synapse related genesHeader

Related codes

  • QA0.0141Syntaxin-binding protein 1-related disorderBillable
  • QA0.0149Neurodevelopmental disorder, related to pathogenic variant in other synapse related geneBillable

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