The search resulted in 48 diseases.
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