Custom Cardiology Panel
Conditions
- Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT)
- Cutis Laxa
- Danon Disease
- Dilated Cardiomyopathy (DCM)
- Ehlers-Danlos Syndrome
- Fabry Disease
- Familial Hypercholesterolemia
- Homocystinuria due to Cystathionine Beta-Synthase Deficiency
- Hypertrophic Cardiomyopathy (HCM)
- Left Ventricular Noncompaction (LVNC)
- Loeys-Dietz syndrome (LDS)
- Long QT Syndrome (LQTS)
- Marfan Syndrome/LDS/Related Disorders
- Multiple Epiphyseal Dysplasia (MED)
- Noonan Syndrome
- Occipital Horn Disease
- Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC)
- Arterial Tortuosity syndrome
- Short QT Syndrome (SQTS)
- Stickler syndrome
- Sudden Cardiac Arrest
- Sudden Unexplained Death
- Thoracic Aortic Aneurysm and Dissection (TAAD) and Related Disorders
- Transthyretin Amyloidosis
- Wolff-Parkinson-White Syndrome
- Non-ocular stickler (STL3) / otospondylomegaepiphyseal dysplasia (OSMED)/ DFNA13/ DFNB53
- Brittle Cornea syndrome
- Brugada Syndrome
- Fibrochondrogenesis
- Marshall syndrome
- Spondyloepiphyseal dysplasia spectrum disorders
- Weissenbach-Zweymuller syndrome
Clinical Utility
- Confirmation of clinical diagnosis in symptomatic patients
- Genetic counseling and risk assessment of asymptomatic family members of a proband with a hereditary cardiovascular condition
Lab Method
- Next-Gen Sequencing
- Deletion/Duplication Analysis
Important Information
Test Code
J779
CPT Codes*
Varies by gene
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.
**Turnaround times are estimates and begin once the sample(s) begin processing at the GeneDx lab and could be extended in situations outside GeneDx’s control.
Test Documents
Billing
Targeted Variant Testing