Genetic disorders, not elsewhere classified (QA0-QA1)

All codes under QA0-QA1

QA0-QA1 can't be used on a claim. Pick a billable code below; grey headings group them.

• QA0Neurodevelopmental disorders related to specific genetic pathogenic variants
• 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
• QA1Genetic disorders associated with neoplasms, not elsewhere classified
• QA1.7Inherited neoplasm predisposition syndromes involving multiple systems, not elsewhere classified
• QA1.71Lynch syndrome
• QA1.79Other inherited neoplasm predisposition syndrome of multiple systems
• QA1.790Familial cancer syndrome with pathogenic BRCA1 mutation
• QA1.791Familial cancer syndrome with pathogenic BRCA2 mutation
• QA1.792Li Fraumeni syndrome
• QA1.798Other inherited neoplasm predisposition syndrome of multiple systems

MS-DRGs

This code does not group to an MS-DRG as a principal diagnosis.