The search resulted in 66 diseases.
Orphanet:101016 Romano-Ward syndrome
Orphanet:111 Barth syndrome
Orphanet:130 Brugada syndrome
Orphanet:1344 Atrial standstill
Orphanet:1359 Carney complex
Orphanet:137675 Histiocytoid cardiomyopathy
Orphanet:217601 Hypertrophic cardiomyopathy due to intensive athletic training
Orphanet:217622 Sensorineural deafness with dilated cardiomyopathy
Orphanet:228140 Idiopathic ventricular fibrillation, not Brugada type
Orphanet:264 Autosomal dominant limb-girdle muscular dystrophy type 1B
Orphanet:26793 Very long chain acyl-CoA dehydrogenase deficiency
Orphanet:300751 Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
Orphanet:324 Fabry disease
Orphanet:3283 His bundle tachycardia
Orphanet:3286 Catecholaminergic polymorphic ventricular tachycardia
Orphanet:329874 Idiopathic giant cell myocarditis
Orphanet:334 Familial atrial fibrillation
Orphanet:3403 Uhl anomaly
Orphanet:34217 Naxos disease
Orphanet:37553 Cardiodysrhythmic potassium-sensitive periodic paralysis
Orphanet:45452 Idiopathic neonatal atrial flutter
Orphanet:51083 Familial short QT syndrome
Orphanet:550 MELAS
Orphanet:563 Peripartum cardiomyopathy
Orphanet:65283 Timothy syndrome
Orphanet:66529 Tako-Tsubo cardiomyopathy
Orphanet:66634 Dilated cardiomyopathy with ataxia
Orphanet:768 Familial long QT syndrome
Orphanet:797 Sarcoidosis
Orphanet:85443 AL amyloidosis
Orphanet:871 Familial progressive cardiac conduction defect
Orphanet:90647 Jervell and Lange-Nielsen syndrome
Orphanet:94062 Coronary artery disease - hyperlipidemia - hypertension - diabetes - osteoporosis
Orphanet:98863 X-linked Emery-Dreifuss muscular dystrophy
Orphanet:98895 Becker muscular dystrophy
Orphanet:98896 Duchenne muscular dystrophy
Orphanet:98909 Desminopathy
OMIM:115197 Cardiomyopathy, familial hypertrophic, 4
OMIM:192500 Long QT syndrome 1
OMIM:192600 Cardiomyopathy, familial hypertrophic, 1
OMIM:600858 Cardiomyopathy, familial hypertrophic, 6
OMIM:600996 Arrhythmogenic right ventricular dysplasia, familial, 2
OMIM:601493 Cardiomyopathy, dilated, 1C
OMIM:601494 Cardiomyopathy, dilated, 1D
OMIM:602087 Arrhythmogenic right ventricular dysplasia, familial, 4
OMIM:603830 Long QT syndrome 3
OMIM:604169 Left ventricular noncompaction 1
OMIM:604400 Arrhythmogenic right ventricular dysplasia, familial, 5
OMIM:604401 Arrhythmogenic right ventricular dysplasia, familial, 6
OMIM:606685 Cardiomyopathy, dilated, 1L
OMIM:607450 Arrhythmogenic right ventricular dysplasia, familial, 8
OMIM:608751 Cardiomyopathy, familial hypertrophic, 8
OMIM:609040 Arrhythmogenic right ventricular dysplasia, familial, 9
OMIM:610193 Arrhythmogenic right ventricular dysplasia, familial, 10
OMIM:610476 Arrhythmogenic right ventricular dysplasia, familial, 11
OMIM:611819 Long QT syndrome 10
OMIM:612124 Cardiomyopathy, familial hypertrophic, 12
OMIM:613172 Cardiomyopathy, dilated, 1DD
OMIM:613688 Long QT syndrome 2
OMIM:613690 Cardiomyopathy, familial hypertrophic, 7
OMIM:613765 Cardiomyopathy, familial hypertrophic, 9
OMIM:614676 Cardiomyopathy, familial hypertrophic, 21
Orphanet:155 Familial isolated hypertrophic cardiomyopathy
OMIM:609470 Left ventricular noncompaction 2
OMIM:615821 Cardiomyopathy, dilated, with woolly hair, keratoderma, and toothagenesis