SE-ATLAS

Familial long QT syndrome Timothy syndrome Inherited isolated arrhythmogenic cardiomyopathy, dominant-left variant Familial dilated cardiomyopathy Dilated cardiomyopathy Mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency Kidney tubulopathy-dilated cardiomyopathy syndrome Neuromuscular disease with dilated cardiomyopathy Mitochondrial disease with dilated cardiomyopathy Inherited isolated arrhythmogenic ventricular dysplasia, biventricular variant Syndrome associated with dilated cardiomyopathy Inherited isolated arrhythmogenic cardiomyopathy, dominant-right variant Fatty acid oxidation and ketogenesis disorder with dilated cardiomyopathy Fixed subaortic stenosis Congenital aortic valve stenosis Sensorineural deafness with dilated cardiomyopathy Interventricular septum aneurysm Congenital Gerbode defect Atrial appendage anomaly Laubry-Pezzi syndrome Aneurysm of sinus of Valsalva Non-familial dilated cardiomyopathy Congenital left ventricular aneurysm Familial restrictive cardiomyopathy Restrictive cardiomyopathy Lysosomal disease with restrictive cardiomyopathy Marfan syndrome type 1 Fatal congenital hypertrophic cardiomyopathy due to glycogen storage disease Peripartum cardiomyopathy Infantile hypertrophic cardiomyopathy due to MRPL44 deficiency Inherited isolated arrhythmogenic cardiomyopathy Cardiomyopathy-cataract-hip spine disease syndrome Mitochondrial DNA-related cardiomyopathy and hearing loss Aorto-ventricular tunnel Dilated cardiomyopathy with ataxia Unclassified cardiomyopathy Ebstein malformation of the tricuspid valve Congenital cataract-hypertrophic cardiomyopathy-mitochondrial myopathy syndrome Congenitally uncorrected transposition of the great arteries Isolated ectopia lentis Early-onset myopathy with fatal cardiomyopathy Lethal left ventricular non-compaction-seizures-hypotonia-cataract-developmental delay syndrome Aortic arch defects Turner syndrome Congenitally corrected transposition of the great arteries Supravalvular aortic stenosis Non-familial restrictive cardiomyopathy Isolated congenitally uncorrected transposition of the great arteries Cardiac diverticulum Romano-Ward syndrome Familial isolated dilated cardiomyopathy Rare familial disorder with hypertrophic cardiomyopathy Congenitally uncorrected transposition of the great arteries with cardiac malformation Non-familial rare disease with dilated cardiomyopathy Familial bicuspid aortic valve Rare congenital non-syndromic heart malformation Hypoplastic right heart syndrome Hypertrophic cardiomyopathy with kidney anomalies due to mitochondrial DNA mutation Rare cardiomyopathy Progressive sensorineural hearing loss-hypertrophic cardiomyopathy syndrome Aorta coarctation Cirrhotic cardiomyopathy Congenital aortic valve dysplasia Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome Criss-cross heart Encephalopathy-hypertrophic cardiomyopathy-renal tubular disease syndrome Erythrokeratodermia-cardiomyopathy syndrome Hypoplastic left heart syndrome Histiocytoid cardiomyopathy Familial dilated cardiomyopathy with conduction defect due to LMNA mutation Microcephaly-cardiomyopathy syndrome Congenital aortic valve atresia Tako-Tsubo cardiomyopathy Rare hypertrophic cardiomyopathy Congenitally uncorrected transposition of the great arteries with coarctation Tetralogy of Fallot Glycogen storage disease with hypertrophic cardiomyopathy Neonatal encephalomyopathy-cardiomyopathy-respiratory distress syndrome Cleft mitral valve Congenital mitral valve insufficiency and/or stenosis Congenital disorder of glycosylation with dilated cardiomyopathy Lysosomal disease with hypertrophic cardiomyopathy Congenital anomaly of the tricuspid valve chordae Mitochondrial disease with hypertrophic cardiomyopathy Parachute tricuspid valve Left ventricular noncompaction Fatty acid oxidation and ketogenesis disorder with hypertrophic cardiomyopathy Inherited arrhythmogenic cardiomyopathy Syndrome associated with hypertrophic cardiomyopathy Univentricular cardiopathy Cardiomyopathy-hypotonia-lactic acidosis syndrome Aortic arch interruption Arterial duct anomaly Non-familial hypertrophic cardiomyopathy Complete atrioventricular septal defect-tetralogy of Fallot Aorto-left ventricular tunnel Aorto-right ventricular tunnel