SE-ATLAS

Familial dilated cardiomyopathy Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency Mucopolysaccharidosis type 2, attenuated form Dilated cardiomyopathy Neuromuscular disease with dilated cardiomyopathy Kidney tubulopathy-dilated cardiomyopathy syndrome 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 Familial atrial tachyarrhythmia-infra-Hisian cardiac conduction disease Sensorineural deafness with dilated cardiomyopathy Jervell and Lange-Nielsen syndrome Non-familial dilated cardiomyopathy Familial restrictive cardiomyopathy Restrictive cardiomyopathy Autosomal dominant Emery-Dreifuss muscular dystrophy Lysosomal disease with restrictive cardiomyopathy MELAS Autosomal recessive Emery-Dreifuss muscular dystrophy MERRF Fatal congenital hypertrophic cardiomyopathy due to glycogen storage disease X-linked Emery-Dreifuss muscular dystrophy Marfan syndrome Acyl-CoA dehydrogenase 9 deficiency Long chain acyl-CoA dehydrogenase deficiency Alpha-sarcoglycan-related limb-girdle muscular dystrophy R3 Alström syndrome Primary hypereosinophilic syndrome Mucopolysaccharidosis type 2 1p36 deletion syndrome HEC syndrome Glycogen storage disease due to acid maltase deficiency, late-onset Dilated cardiomyopathy with ataxia Unclassified cardiomyopathy Becker muscular dystrophy Familial abdominal aortic aneurysm Friedreich ataxia Early-onset myopathy with fatal cardiomyopathy Nathalie syndrome Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome Barth syndrome Beckwith-Wiedemann syndrome Loeys-Dietz syndrome Brugada syndrome Noonan syndrome-like disorder with loose anagen hair Ocular anomalies-axonal neuropathy-developmental delay syndrome Familial isolated dilated cardiomyopathy Peripartum cardiomyopathy Duchenne muscular dystrophy Ehlers-Danlos syndrome with periventricular heterotopia Desminopathy Lymphocytic hypereosinophilic syndrome Leber hereditary optic neuropathy Combined oxidative phosphorylation defect type 23 Beta-mannosidosis Beta-sarcoglycan-related limb-girdle muscular dystrophy R4 Polyglucosan body myopathy type 1 Non-familial restrictive cardiomyopathy Noonan syndrome Congenital heart block Romano-Ward syndrome Non-familial rare disease with dilated cardiomyopathy Systemic primary carnitine deficiency Carnitine-acylcarnitine translocase deficiency Multiple acyl-CoA dehydrogenase deficiency Very long chain acyl-CoA dehydrogenase deficiency Progressive sensorineural hearing loss-hypertrophic cardiomyopathy syndrome His bundle tachycardia Alpha-B crystallin-related late-onset myopathy Beckwith-Wiedemann syndrome due to 11p15 microdeletion Catecholaminergic polymorphic ventricular tachycardia Beckwith-Wiedemann syndrome due to 11p15 translocation/inversion Fukutin-related limb-girdle muscular dystrophy R13 Delta-sarcoglycan-related limb-girdle muscular dystrophy R6 Sinoatrial node dysfunction and deafness Familial aortic dissection Mitochondrial trifunctional protein deficiency Diffuse cutaneous systemic sclerosis Sino-auricular heart block Limited cutaneous systemic sclerosis 46,XY complete gonadal dysgenesis Fatal infantile hypertrophic cardiomyopathy due to mitochondrial complex I deficiency Adult polyglucosan body disease Limited systemic sclerosis Pseudoxanthoma elasticum Inherited arrhythmogenic cardiomyopathy Familial thoracic aortic aneurysm and aortic dissection Combined oxidative phosphorylation defect type 17 Familial long QT syndrome Duchenne and Becker muscular dystrophy Autosomal dominant limb-girdle muscular dystrophy type 1B Mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency Arterial tortuosity syndrome Steinert myotonic dystrophy Chronic atrial and intestinal dysrhythmia syndrome Wild type ATTR amyloidosis Glycogen storage disease due to LAMP-2 deficiency Sarcoidosis Vascular Ehlers-Danlos syndrome Hurler syndrome Multiple acyl-CoA dehydrogenase deficiency, mild type Hurler-Scheie syndrome Multiple acyl-CoA dehydrogenase deficiency, severe neonatal type Marfan syndrome type 1 Marfan syndrome type 2 Tropical endomyocardial fibrosis Loeffler endocarditis Idiopathic ventricular fibrillation, non Brugada type Infantile hypertrophic cardiomyopathy due to MRPL44 deficiency Isobutyryl-CoA dehydrogenase deficiency Neonatal Marfan syndrome Aneurysm-osteoarthritis syndrome Cardiofaciocutaneous syndrome Heart-hand syndrome type 3 X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome Atrial standstill Cardiomyopathy-cataract-hip spine disease syndrome DPM3-CDG Mitochondrial DNA-related cardiomyopathy and hearing loss Heart-hand syndrome type 2 Primary systemic amyloidosis Uhl anomaly Glycogen storage disease due to acid maltase deficiency, infantile onset Lown-Ganong-Levine syndrome Beckwith-Wiedemann syndrome due to 11p15 microduplication Familial atrial fibrillation Primary localized amyloidosis Rare disease with thoracic aortic aneurysm and aortic dissection Congenital cataract-hypertrophic cardiomyopathy-mitochondrial myopathy syndrome Fucosidosis Heart-hand syndrome, Slovenian type Gamma-sarcoglycan-related limb-girdle muscular dystrophy R5 Lethal left ventricular non-compaction-seizures-hypotonia-cataract-developmental delay syndrome Familial progressive cardiac conduction defect Glycogen storage disease due to acid maltase deficiency Glycogen storage disease due to glycogen debranching enzyme deficiency Glycogen storage disease due to glycogen branching enzyme deficiency LIMS2-related myopathy Brachydactyly-long thumb syndrome Diabetic embryopathy Leber plus disease Holt-Oram syndrome Familial sick sinus syndrome Glycogen storage disease due to glycogen branching enzyme deficiency, progressive hepatic form Familial short QT syndrome Torsade-de-pointes syndrome with short coupling interval Glycogen storage disease due to glycogen branching enzyme deficiency, non progressive hepatic form Rare familial disorder with hypertrophic cardiomyopathy Glycogen storage disease due to muscle and heart glycogen synthase deficiency Beckwith-Wiedemann syndrome due to paternal uniparental disomy of chromosome 11 Noonan syndrome-like disorder with juvenile myelomonocytic leukemia AL amyloidosis AA amyloidosis Atrial septal defect-atrioventricular conduction defects syndrome Erythrokeratodermia-cardiomyopathy syndrome Glycogen storage disease due to glycogen branching enzyme deficiency, childhood combined hepatic and myopathic form Histiocytoid cardiomyopathy Gaucher disease type 1 ATTRV122I amyloidosis Gaucher disease type 3 Microcephaly-cardiomyopathy syndrome Vici syndrome Glycogen storage disease due to glycogen branching enzyme deficiency, childhood neuromuscular form Kearns-Sayre syndrome Tako-Tsubo cardiomyopathy Endocardial fibroelastosis Neonatal encephalomyopathy-cardiomyopathy-respiratory distress syndrome Multisystemic smooth muscle dysfunction syndrome Congenital disorder of glycosylation with dilated cardiomyopathy Lysosomal disease with hypertrophic cardiomyopathy Mitochondrial disease with hypertrophic cardiomyopathy Familial isolated restrictive cardiomyopathy Noonan syndrome with multiple lentigines DK1-CDG Syndrome de cardiomyopathie-hypotonie-acidose lactique Cardiomyopathie hypertrophique non familiale Syndrome hyperéosinophilique Mucopolysaccharidose type 2, forme sévère Anomalie de l'oxydation des acides gras et de la cétogenèse avec cardiomyopathie hypertrophique Non-compaction ventriculaire gauche Syndrome de Costello Syndrome de Beckwith-Wiedemann dû à une mutation de NSD1 Syndrome hyperéosinophilique secondaire Myocardite idiopathique à cellules géantes Sclérodermie systémique Syndrome de cardiomyopathie dilatée-hypogonadisme hypergonadotrope Syndrome d'encéphalopathie-cardiomyopathie hypertrophique-néphropathie tubulaire Cardiomyopathie dilatée familiale avec trouble de la conduction due à une mutation de LMNA Forme symptomatique de la dystrophie musculaire de Duchenne et Becker de la femme porteuse Syndrome de Carvajal Dystrophie musculaire d'Emery-Dreifuss Cardiomyopathie rare Syndrome de McLeod Glycogénose par déficit en enzyme branchante, forme neuromusculaire périnatale fatale Cardiomyopathie cirrhotique Glycogénose par déficit en enzyme branchante, forme neuromusculaire congénitale Cardiomyopathie hypertrophique rare Maladie de stockage du glycogène avec cardiomyopathie hypertrophique Syndrome associé à une cardiomyopathie hypertrophique Cardiomyopathie hypertrophique due à un entraînement athlétique intensif Cardiomyopathie arythmogène héréditaire isolée, variante gauche-dominante Trouble génétique du rythme cardiaque Cardiomyopathie arythmogène héréditaire isolée PGM1-CDG Bicuspidie aortique familiale Syndrome d'Andersen-Tawil Syndrome CREST Granulomatose éosinophilique avec polyangéite Syndrome de Timothy Cardiomyopathie hypertrophique avec anomalies rénales dues à une mutation de l'ADN mitochondrial Glycogénose par déficit en enzyme branchante de l'adulte, forme neuromusculaire Syndrome hyperéosinophilique idiopathique Syndrome de Beckwith-Wiedemann dû à un défaut d'empreinte de la région 11p15 Syndrome de Beckwith-Wiedemann dû à une mutation de CDKN1C Maladie de Naxos Dystrophie musculaire des ceintures associée à BVES