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QA0 Neurodevelopmental disorders related to specific genetic pathogenic variants

Non-Billable/Non-Specific

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.-)

Codes

  • QA0.0Neurodevelopmental disorders related to pathogenic variants in specific genes
    • QA0.01Neurodevelopmental disorders related to pathogenic variants in certain specific genes
      • QA0.010Neurodevelopmental disorders, related to pathogenic variants in ion channel genes
        • QA0.0101SCN2A-related neurodevelopmental disorder
        • QA0.0102CACNA1A-related neurodevelopmental disorder
        • QA0.0109Neurodevelopmental disorder related to pathogenic variant in other ion channel gene
      • QA0.011Neurodevelopmental disorders, related to pathogenic variants in glutamate receptor genes
      • QA0.012Neurodevelopmental disorders, related to pathogenic variants in other receptor genes
      • QA0.013Neurodevelopmental disorders, related to pathogenic variants in other transporter and solute carrier genes
        • QA0.0131SLC6A1-related disorder
        • QA0.0139Neurodevelopmental disorder, related to pathogenic variant in other transporter or solute carrier gene
      • QA0.014Neurodevelopmental disorders, related to pathogenic variants in synapse related genes
        • QA0.0141Syntaxin-binding protein 1-related disorder
        • QA0.0142DLG4-related synaptopathy
        • QA0.0149Neurodevelopmental disorder, related to pathogenic variant in other synapse related gene
      • QA0.015Neurodevelopmental disorders, related to genes associated with transcription and gene expression
        • QA0.0151FOXG1 syndrome
        • QA0.0159Neurodevelopmental disorder, related to other genes associated with transcription and gene expression
  • QA0.8Other neurodevelopmental disorders related to pathogenic variants in other specific genes