QA0.0141BillableCCNo HCCPOA Exempt

Syntaxin-binding protein 1-related disorder

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

Also indexed as: Disorder, neurodevelopmental, STXBP1-related; Disorder, neurodevelopmental, syntaxin-binding protein 1-related

Instructional notes

Includes: conditions that are coded here

  • STXBP1-related disorders

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 QA0.0141.

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)