genetic disease of the heart
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More general terms
More specific terms
- atrial septal defect type 2 (ASD2)
- atrial septal defect type 3 (ASD3)
- atrial septal defect type 4 (ASD3)
- atrial septal defect type 5 (ASD5)
- atrial septal defect type 6 (ASD6)
- catecholaminergic polymorphic ventricular tachycardia; stress-induced polymorphic ventricular tachycardia
- conotruncal heart malformation
- dilated cardiomyopathy with quadriceps myopathy
- early repolarization syndrome
- familial arrhythmogenic right ventricular dysplasia; arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVD, ARVC, ARVD/C, ARVC/D)
- familial heart block
- familial hypertrophic cardiomyopathy
- familial polymorphic ventricular tachycardia
- inherited form of coronary artery disease
- Jervell & Lange-Nielsen syndrome
- long QT syndrome
- non-compaction of left ventricular myocardium (left ventricular non-compaction)
- Noonan's syndrome
- paroxysmal familial ventricular fibrillation; idiopathic ventricular fibrillation
- short QT syndrome