Asper Cardiogenetics
Apolipoprotein C-II Deficiency
Arrhythmia UPDATED
Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy UPDATED
Brugada Syndrome UPDATED
Catecholaminergic Polymorphic Ventricular Tachycardia
Dilated Cardiomyopathy UPDATED
Ehlers-Danlos Syndrome
Familial Hypercholesterolemia
Familial Lipoprotein Lipase Deficiency
Familial Thoracic Aortic Aneurysms and Dissections and Related Syndromes
Hereditary Hemorrhagic Telangiectasia
Hyperlipoproteinemia, type 3
Hyperlipoproteinemia, type 5
Hypertriglyceridemia
Hypertrophic Cardiomyopathy
Lecithin Cholesterol Acyltransferase Deficiency
Left Ventricular Noncompaction Cardiomyopathy NEW
Long QT Syndrome
Mitochondrial diseases
Noonan Spectrum Disorders/Rasopathies UPDATED
Pulmonary Arterial Hypertension
Short QT Syndrome
Statin-Induced Myopathy
Tangier Disease
Thrombophilia
Whole Exome Sequencing
Asper Cardiogenetics covers genetic tests related to cardiovascular diseases, including Long QT syndrome, Marfan syndrome, Noonan 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.