Hereditary Cardiovascular Testing

Ambry’s hereditary cardiovascular testing menu includes multi-gene panels and single gene testing for inherited arrhythmias, cardiomyopathies, aortic aneurysms/dissections, Marfan syndrome, Ehlers-Danlos syndromes, and familial hypercholesterolemia.

Our inherited arrhythmia and cardiomyopathy panels feature an intuitive, tiered approach for hypertrophic cardiomyopathy, long QT syndrome, and Brugada syndrome. Establishing a molecular diagnosis for inherited cardiovascular conditions can be life-saving; genetic test results can direct and improve patient management, and target surveillance for cardiovascular complications.

 

Hereditary Cardiovascular Panels

Test Code Test Name Description TAT (weeks)
8888 RhythmFirst (3 genes) First-tier test of 3 genes for long QT syndrome, Brugada syndrome, short QT syndrome 2-3
8900 RhythmNext (36 genes) 36 genes for long QT syndrome, Brugada syndrome, other inherited arrhythmias 4-5
8902 CPVTNext (6 genes) 6 genes for catecholaminergic polymorphic ventricular tachycardia (CPVT) 4-5
8904 ARVDNext (9 genes) 9 genes for arrhythmogenic right ventricular dysplasia (ARVD) 4-5
8935 HCMFirst (2 genes) First-tier test of 2 most common genes for hypertrophic cardiomyopathy (HCM) 2-3
8936 HCMNext (27 genes) 27 genes for hypertrophic cardiomyopathy (HCM) 4-5
8884 DCMNext (36 genes) 36 genes for dilated cardiomyopathy (DCM) 4-5
8906 LVNCNext (8 genes) 8 genes for left-ventricular non-compaction (LVNC) 4-5
8886 CMNext (54 genes) 54 genes for inherited cardiomyopathy 4-5
8887 CMNext+ TTN (55 genes) 55 genes for inherited cardiomyopathy 4-5
8910 CardioNext (84 genes) 84 genes for inherited cardiomyopathies and arrhythmias 4-5
8911 CardioNext+TTN (85 genes) 85 genes for inherited cardiomyopathies and arrhythmias 4-5
8789 TAADNext 22 genes for Marfan syndrome, thoracic aortic aneurysms and dissections (TAAD), related disorders 2-4
8680 FHNext (3 genes) 3 genes for familial hypercholesterolemia 2-3

You can view a complete listing of Ambry's testing options organized by disease here, and organized by gene here.