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QA0.0109BillableSave

QA0.0109 - Neurodevelopmental disorder related to pathogenic variant in other ion channel gene

ICD-10-CM Chapter 17: Congenital malformations, deformations and chromosomal abnormalities · QA0-QA1 Genetic disorders, not elsewhere classified (QA0-QA1) · Subcategory of QA0.010 · FY2027

Applicable To

Inclusion terms listed under QA0.0109 in the ICD-10-CM tabular list.

  • SCN8A-related neurodevelopmental disorder

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