Conditions List - Cardiovascular
Condition
- Amyloidosis, Hereditary, Transthyretin-Related
- Aortic Aneurysm, Familial Thoracic 4
- Aortic Aneurysm, Familial Thoracic 6
- Arrhythmogenic Right Ventricular Cardiomyopathy, Type 5
- Arrhythmogenic Right Ventricular Cardiomyopathy, Type 8
- Arrhythmogenic Right Ventricular Cardiomyopathy, Type 9
- Arrhythmogenic Right Ventricular Cardiomyopathy, Type 10
- Arrhythmogenic Right Ventricular Cardiomyopathy, Type 11
- Arterial Calcification, Generalized, of Infancy, 1
- Arterial Calcification, Generalized, of Infancy, 2
- Barth Syndrome
- Cardiomyopathy, Dilated, 1AA, with or without LVNC
- Cardiomyopathy, Dilated, 1D
- Cardiomyopathy, Dilated, 1R
- Cardiomyopathy, Familial Hypertrophic, 11
- Cardiomyopathy, Familial Hypertrophic, 26
- Cardiomyopathy, Familial Hypertrophic, 9
- Combined Oxidative Phosphorylation Deficiency 8
- Dilated Cardiomyopathy 1A
- Dilated Cardiomyopathy 1E
- Dilated Cardiomyopathy 3B
- Ehlers-Danlos Syndrome, Vascular Type
- Familial Hypertrophic Cardiomyopathy 1
- Familial Hypertrophic Cardiomyopathy 10
- Familial Hypertrophic Cardiomyopathy 11
- Familial Hypertrophic Cardiomyopathy 3
- Familial Hypertrophic Cardiomyopathy 4
- Familial Hypertrophic Cardiomyopathy 6
- Familial Hypertrophic Cardiomyopathy 7
- Familial Hypertrophic Cardiomyopathy 8
- Heterotaxy, Visceral, 1, X-Linked
- Heterotaxy, Visceral, 4, Autosomal
- Liddle Syndrome 1
- Liddle Syndrome 2
- Loeys-Dietz Syndrome 1
- Loeys-Dietz Syndrome 2
- Loeys-Dietz Syndrome Type 3
- Long QT Syndrome 1
- Long QT Syndrome 2
- Long QT Syndrome 3
- Long QT Syndrome 5
- Marfan Syndrome
- Mitochondrial Complex I Deficiency nuclear type 20
- Supravalvular Aortic Stenosis
- Telangiectasia, Hereditary Hemorrhagic, Type 1
- Telangiectasia, Hereditary Hemorrhagic, Type 2
- Tetralogy Of Fallot
- Ventricular Arrhythmias
- Ventricular Tachycardia, Catecholaminergic Polymorphic, 1
- Ventricular Tachycardia, Catecholaminergic Polymorphic, 2
- Ventricular Tachycardia, Catecholaminergic Polymorphic, 5