SE-ATLAS

Inherited isolated arrhythmogenic cardiomyopathy, dominant-left variant HEC syndrome Unclassified cardiomyopathy Generalized congenital lipodystrophy with myopathy Brugada syndrome Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers Familial long QT syndrome Timothy syndrome Familial atrial fibrillation Carney complex Torsade-de-pointes syndrome with short coupling interval Idiopathic neonatal atrial flutter Conotruncal heart malformations Familial restrictive cardiomyopathy Autosomal dominant Emery-Dreifuss muscular dystrophy Fatal congenital hypertrophic cardiomyopathy due to glycogen storage disease Multifocal atrial tachycardia Steinert myotonic dystrophy Pulmonary arterial hypertension associated with congenital heart disease Carney complex-trismus-pseudocamptodactyly syndrome Naxos disease Eisenmenger syndrome Rare hypertrophic cardiomyopathy Inherited isolated arrhythmogenic cardiomyopathy, dominant-right variant Lysosomal disease with restrictive cardiomyopathy X-linked Emery-Dreifuss muscular dystrophy Andersen-Tawil syndrome Complete atrioventricular septal defect with ventricular hypoplasia Tropical endomyocardial fibrosis Truncus arteriosus Lethal left ventricular non-compaction-seizures-hypotonia-cataract-developmental delay syndrome Primary adult heart tumor Rare familial disorder with hypertrophic cardiomyopathy Idiopathic/heritable pulmonary arterial hypertension Cirrhotic cardiomyopathy Tako-Tsubo cardiomyopathy Endocardial fibroelastosis Glycogen storage disease with hypertrophic cardiomyopathy Congenital disorder of glycosylation with dilated cardiomyopathy Inherited isolated arrhythmogenic ventricular dysplasia, biventricular variant ATTRV122I amyloidosis