QA0.0131

SLC6A1-related disorder

Billable / specificPOA exempt

QA0.0131 is a billable, specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes in FY2027.

Inclusion terms

Applicable to

  • GABA transporter 1 deficiency

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

  • GABA transporter 1 deficiency
  • Deficiency, deficient, GABA transporter 1
  • Disorder, neurodevelopmental, SLC6A1-related

Parent code

  • QA0.013Neurodevelopmental disorders, related to pathogenic variants in other transporter and solute carrier genesHeader

Related codes

  • QA0.0139Neurodevelopmental disorder, related to pathogenic variant in other transporter or solute carrier geneBillable

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