QA0-QA1 ICD-10-CM Codes: Genetic disorders, not elsewhere classified

Neurodevelopmental disorders related to specific genetic pathogenic variants

Neurodevelopmental disorders related to pathogenic variants in specific genes

Neurodevelopmental disorders related to pathogenic variants in certain specific genes

Neurodevelopmental disorders, related to pathogenic variants in ion channel genes

SCN2A-related neurodevelopmental disorder

CACNA1A-related neurodevelopmental disorder

Neurodevelopmental disorder related to pathogenic variant in other ion channel gene

Neurodevelopmental disorders, related to pathogenic variants in glutamate receptor genes

Neurodevelopmental disorders, related to pathogenic variants in other receptor genes

Neurodevelopmental disorders, related to pathogenic variants in other transporter and solute carrier genes

SLC6A1-related disorder

Neurodevelopmental disorder, related to pathogenic variant in other transporter or solute carrier gene

Neurodevelopmental disorders, related to pathogenic variants in synapse related genes

Syntaxin-binding protein 1-related disorder

DLG4-related synaptopathy

Neurodevelopmental disorder, related to pathogenic variant in other synapse related gene

Neurodevelopmental disorders, related to genes associated with transcription and gene expression

FOXG1 syndrome

Neurodevelopmental disorder, related to other genes associated with transcription and gene expression

Other neurodevelopmental disorders related to pathogenic variants in other specific genes

Genetic disorders associated with neoplasms, not elsewhere classified

Inherited neoplasm predisposition syndromes involving multiple systems, not elsewhere classified

Lynch syndrome

Other inherited neoplasm predisposition syndrome of multiple systems

Familial cancer syndrome with pathogenic BRCA1 mutation

Familial cancer syndrome with pathogenic BRCA2 mutation

Li Fraumeni syndrome

Other inherited neoplasm predisposition syndrome of multiple systems