SE-ATLAS

Cardiomyopathie arythmogène héréditaire isolée, variante gauche-dominante Syndrome HEC Cardiomyopathie non classée Lipodystrophie congénitale généralisée avec myopathie Syndrome de Brugada Forme symptomatique de la dystrophie musculaire de Duchenne et Becker de la femme porteuse Syndrome du QT long familial Syndrome de Timothy Fibrillation auriculaire familiale Complexe de Carney Syndrome des torsades de pointes à couplage court Flutter auriculaire idiopathique du nouveau-né Malformation cardiaque conotroncale Cardiomyopathie familiale restrictive Dystrophie musculaire d'Emery-Dreifuss autosomique dominante Cardiomyopathie hypertrophique congénitale létale par maladie de stockage du glycogène 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