QA0.0149BillableCCNo HCCPOA Exempt

Neurodevelopmental disorder, related to pathogenic variant in other synapse related gene

Congenital Malformations, Deformations and Chromosomal Abnormalities·Neurodevelopmental disorders, related to pathogenic variants in synapse related genes·subcategory·FY 2027

Also indexed as: Disorder, neurodevelopmental, other, synapse related gene; Synaptopathy, specified NEC

Instructional notes

Includes: conditions that are coded here

  • Other genetic synaptopathy

Also applies, from QA0: Neurodevelopmental disorders related to specific genetic pathogenic variants

These notes sit on QA0 and apply to every code under it, including QA0.0149.

Code also: add a code for this too, order depends on the encounter

  • 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.-)

MS-DRGs

As the principal diagnosis, this code groups to these MS-DRGs (v44.0). Which one applies depends on procedures performed, secondary diagnoses (CC/MCC), and the patient's age and discharge status.

Code history

  • FY 2025: replaced F89 (Unspecified disorder of psychological development)