The search resulted in 48 diseases.
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| Orphanet:130 | Brugada syndrome | ||
| Orphanet:1479 | Atrial septal defect - atrioventricular conduction defects syndrome | ||
| Orphanet:228429 | Generalized congenital lipodystrophy with myopathy | ||
| Orphanet:273 | Steinert myotonic dystrophy | ||
| Orphanet:300751 | Familial dilated cardiomyopathy with conduction defect due to LMNA mutation | ||
| Orphanet:3071 | Costello syndrome | ||
| Orphanet:324 | Fabry disease | ||
| Orphanet:324410 | X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome | ||
| Orphanet:3286 | Catecholaminergic polymorphic ventricular tachycardia | ||
| Orphanet:329874 | Idiopathic giant cell myocarditis | ||
| Orphanet:334 | Familial atrial fibrillation | ||
| Orphanet:54260 | Left ventricular noncompaction | ||
| Orphanet:59306 | McLeod neuroacanthocytosis syndrome | ||
| Orphanet:75249 | Familial isolated restrictive cardiomyopathy | ||
| Orphanet:75565 | Tropical endomyocardial fibrosis | ||
| Orphanet:75566 | Loeffler endocarditis | ||
| Orphanet:85443 | AL amyloidosis | ||
| Orphanet:85451 | ATTRV122I amyloidosis | ||
| Orphanet:98855 | Autosomal recessive Emery-Dreifuss muscular dystrophy | ||
| Orphanet:98863 | X-linked Emery-Dreifuss muscular dystrophy | ||
| Orphanet:98909 | Desminopathy | ||
| OMIM:145350 | Hypertaurinuric cardiomyopathy | ||
| OMIM:182190 | Sinus node disease and myopia | ||
| OMIM:229300 | Friedreich ataxia 1 | ||
| OMIM:600858 | Cardiomyopathy, familial hypertrophic, 6 | ||
| OMIM:601154 | Cardiomyopathy, dilated, 1E | ||
| OMIM:601494 | Cardiomyopathy, dilated, 1D | ||
| OMIM:602086 | Arrhythmogenic right ventricular dysplasia, familial, 3 | ||
| OMIM:604169 | Left ventricular noncompaction 1 | ||
| OMIM:607554 | Atrial fibrillation, familial, 3 | ||
| OMIM:612158 | Cardiomyopathy, dilated, 1AA with or without left ventricular noncompaction | ||
| OMIM:612422 | Cardiomyopathy, familial restrictive, 3 | ||
| OMIM:612877 | Cardiomyopathy, dilated, 1BB | ||
| OMIM:613172 | Cardiomyopathy, dilated, 1DD | ||
| OMIM:613424 | Cardiomyopathy, dilated, 1R | ||
| OMIM:613426 | Cardiomyopathy, dilated, 1S | ||
| OMIM:613690 | Cardiomyopathy, familial hypertrophic, 7 | ||
| OMIM:613838 | Cardiomyopathy, familial hypertrophic, 16 | ||
| OMIM:613874 | Cardiomyopathy, familial hypertrophic, 18 | ||
| OMIM:613876 | Cardiomyopathy, familial hypertrophic, 20 | ||
| OMIM:613881 | Cardiomyopathy, dilated, 1HH | ||
| OMIM:614672 | Cardiomyopathy, dilated, 2B | ||
| Orphanet:155 | Familial isolated hypertrophic cardiomyopathy | ||
| Orphanet:435988 | Chronic atrial and intestinal dysrhythmia syndrome | ||
| OMIM:615248 | Cardiomyopathy, dilated, 1KK | ||
| Orphanet:436242 | Familial atrial tachyarrhythmia-infra-Hisian cardiac conduction disease | ||
| OMIM:609578 | Cardiomyopathy, familial restrictive 2 | ||
| OMIM:617047 | CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 26 |