QA0.0101 SCN2A-RELATED NEURODEVELOPMENTAL DISORDER

Code Information

  • Diagnosis Code: QA0.0101
  • Short Description: SCN2A-related neurodevelopmental disorder
  • Long Description: SCN2A-related neurodevelopmental disorder
  • Code Version: 2025 ICD-10-CM

The code QA0.0101 is VALID for claim submission

Code Classification

Diagnostic Related Group(s)

The code QA0.0101 is grouped in the following Diagnostic Related Group(s) MS-DRG V43.0

  1. Other Musculoskeletal System And Connective Tissue Diagnoses With Mcc (564)
  2. Other Musculoskeletal System And Connective Tissue Diagnoses With Cc (565)
  3. Other Musculoskeletal System And Connective Tissue Diagnoses Without Cc/mcc (566)

Similar Codes

ICD-10 Code ICD-10 Description
QA0 Neurodevelopmental disorders related to specific genetic pathogenic variants
QA0.0 Neurodevelopmental disorders related to pathogenic variants in specific genes
QA0.01 Neurodevelopmental disorders related to pathogenic variants in certain specific genes
QA0.010 Neurodevelopmental disorders, related to pathogenic variants in ion channel genes
QA0.0102 CACNA1A-related neurodevelopmental disorder
QA0.0109 Neurodevelopmental disorder related to pathogenic variant in other ion channel gene
QA0.011 Neurodevelopmental disorders, related to pathogenic variants in glutamate receptor genes
QA0.012 Neurodevelopmental disorders, related to pathogenic variants in other receptor genes
QA0.013 Neurodevelopmental disorders, related to pathogenic variants in other transporter and solute carrier genes
QA0.0131 SLC6A1-related disorder
QA0.0139 Neurodevelopmental disorder, related to pathogenic variant in other transporter or solute carrier gene
QA0.014 Neurodevelopmental disorders, related to pathogenic variants in synapse related genes
QA0.0141 Syntaxin-binding protein 1-related disorder
QA0.0142 DLG4-related synaptopathy
QA0.0149 Neurodevelopmental disorder, related to pathogenic variant in other synapse related gene
QA0.015 Neurodevelopmental disorders, related to genes associated with transcription and gene expression
QA0.0151 FOXG1 syndrome
QA0.0159 Neurodevelopmental disorder, related to other genes associated with transcription and gene expression
QA0.8 Other neurodevelopmental disorders related to pathogenic variants in other specific genes
This page was last updated on: 10/1/2025
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