QA0.01
Neurodevelopmental disorders related to pathogenic variants in certain specific genes
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- QA0.010Neurodevelopmental disorders, related to pathogenic variants in ion channel genesMore levels
- QA0.011Neurodevelopmental disorders, related to pathogenic variants in glutamate receptor genesBillable
- QA0.012Neurodevelopmental disorders, related to pathogenic variants in other receptor genesBillable
- QA0.013Neurodevelopmental disorders, related to pathogenic variants in other transporter and solute carrier genesMore levels
- QA0.014Neurodevelopmental disorders, related to pathogenic variants in synapse related genesMore levels
- QA0.015Neurodevelopmental disorders, related to genes associated with transcription and gene expressionMore levels
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
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