Forms and Documents
- Molecular confirmation of a clinical diagnosis in symptomatic patients
- Risk assessment of asymptomatic family members of a proband with cardiomyopathy
- Differentiation of hereditary cardiomyopathy from acquired (non-genetic) cardiomyopathy
- Recurrence risk calculation
*Reporting times are typical, but could be extended in situations outside GeneDx's reasonable control.
**The CPT codes provided are based on AMA guidelines and are for informational purposes only. CPT coding is the sole responsibility of the billing party. Please direct any questions regarding coding to the payer being billed.