QA0.0149
Neurodevelopmental disorder, related to pathogenic variant in other synapse related gene
Billable code
This code does not map to a risk-adjusting HCC in the loaded models.
Coding notes
Excludes 1 never coded together · Excludes 2 may co-exist
This code · QA0.0149
Synonyms
Other genetic synaptopathy
Inherited from QA0Neurodev disord related to specific genetic patho variants
Code also
, 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.-)
Inherited from chapter 17Congenital malformations, deformations and chromosomal abnormalities
Excludes 2
inborn errors of metabolism (E70-E88)
Note
Codes from this chapter are not for use on maternal records
Official Guidelines for QA0.0149
FY 2026 ›Find QA0.0149 in the alphabetic index
2 index paths lead to this code