Cardiomyopathy Panel
New York
Approved
Genes
Conditions
- Dilated Cardiomyopathy (DCM)
- Hypertrophic Cardiomyopathy (HCM)
- Left Ventricular Noncompaction (LVNC)
- Noonan Syndrome
- Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC)
Clinical Utility
- 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
Lab Method
- Deletion/Duplication Analysis
- Next-Gen Sequencing
Test Code
694
CPT Codes*
81439x1
ABN Required
No
Turnaround Time**
4 weeks
Preferred Specimen
Alternative Specimen
*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.
**Reporting times are typical and begin once the sample(s) are received at the GeneDx laboratory, but could be extended in situations outside GeneDx’s reasonable control.
Test Documents
Billing
For Providers
Targeted Variant Testing