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QA0.0159 Neurodevelopmental disorder, related to other genes associated with transcription and gene expression
BackQA0Neurodevelopmental disorders related to specific genetic pathogenic variantsCategory3 →QA0.0Neurodevelopmental disorders related to pathogenic variants in specific genesCategory1 →QA0.01Neurodevelopmental disorders related to pathogenic variants in certain specific genesCategory6 →QA0.010Neurodevelopmental disorders, related to pathogenic variants in ion channel genesCategory3 →QA0.0101SCN2A-related neurodevelopmental disorderCategoryQA0.0102CACNA1A-related neurodevelopmental disorderCategoryQA0.0109Neurodevelopmental disorder related to pathogenic variant in other ion channel geneCategoryQA0.011Neurodevelopmental disorders, related to pathogenic variants in glutamate receptor genesCategoryQA0.012Neurodevelopmental disorders, related to pathogenic variants in other receptor genesCategoryQA0.013Neurodevelopmental disorders, related to pathogenic variants in other transporter and solute carrier genesCategory2 →QA0.0131SLC6A1-related disorderCategoryQA0.0139Neurodevelopmental disorder, related to pathogenic variant in other transporter or solute carrier geneCategoryQA0.014Neurodevelopmental disorders, related to pathogenic variants in synapse related genesCategory3 →QA0.0141Syntaxin-binding protein 1-related disorderCategoryQA0.0142DLG4-related synaptopathyCategoryQA0.0149Neurodevelopmental disorder, related to pathogenic variant in other synapse related geneCategoryQA0.015Neurodevelopmental disorders, related to genes associated with transcription and gene expressionCategory2 →QA0.0151FOXG1 syndromeCategoryQA0.0159Neurodevelopmental disorder, related to other genes associated with transcription and gene expressionCategoryQA0.8Other neurodevelopmental disorders related to pathogenic variants in other specific genesCategory
CategoryCODABLE
QA0.0159
Neurodevelopmental disorder, related to other genes associated with transcription and gene expression
- Chapter
- XVII · Congenital malformations, deformations, chromosomal abnormalities, and genetic disorders
- Section
- QA0
- Valid from
Source
CMS ICD-10-CM Tabular List, edition FY2026.