SLN Cardiogenetics

Apolipoprotein C-II Deficiency
Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy
Brugada Syndrome
Catecholaminergic Polymorphic Ventricular Tachycardia
Dilated Cardiomyopathy
Ehlers-Danlos Syndrome
Familial Hypercholesterolemia
Familial Lipoprotein Lipase Deficiency
Familial Thoracic Aortic Aneurysms and Dissections and Related Syndromes UPDATED
Hereditary Hemorrhagic Telangiectasia
Hyperlipoproteinemia, type 3
Hyperlipoproteinemia, type 5
Hypertrophic Cardiomyopathy
Lecithin Cholesterol Acyltransferase Deficiency
Long QT Syndrome
Noonan Spectrum Disorders/Rasopathies
Pulmonary Arterial Hypertension
Short QT Syndrome
Statin-Induced Myopathy
Tangier Disease
Whole Exome Sequencing


SLN Cardiogenetics covers genetic tests related to cardiovascular diseases, including Long QT syndromeMarfan syndromeNoonan syndrome, as well as tests for prediction of adverse drug reactions.

Determining the genetic causes of inherited heart diseases provides valuable insight for molecular confirmation of clinical diagnosis, differential diagnosis of related disorders, and risk assessment of family members.

Genetic heart conditions assembled in this testing menu are detectable mainly by multi-gene panels, but yet single gene testing and targeted mutation analysis are also available.