The search resulted in 64 diseases.
Orphanet:101016 Romano-Ward syndrome
Orphanet:101934 Genetic cardiac rhythm disease
Orphanet:1260 Sino-auricular heart block
Orphanet:130 Brugada syndrome
Orphanet:1342 Heart-hand syndrome type 3
Orphanet:1344 Atrial standstill
Orphanet:1350 Heart-hand syndrome type 2
Orphanet:137675 Histiocytoid cardiomyopathy
Orphanet:1479 Atrial septal defect - atrioventricular conduction defects syndrome
Orphanet:166282 Familial sick sinus syndrome
Orphanet:168796 Heart-hand syndrome, Slovenian type
Orphanet:218439 Non-genetic cardiac rhythm disease
Orphanet:228012 Progressive sensorineural hearing loss-hypertrophic cardiomyopathy syndrome
Orphanet:228140 Idiopathic ventricular fibrillation, not Brugada type
Orphanet:228429 Generalized congenital lipodystrophy with myopathy
Orphanet:2946 Brachydactyly-long thumb syndrome
Orphanet:324321 Sinoatrial node dysfunction and deafness
Orphanet:324410 X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome
Orphanet:3282 Multifocal atrial tachycardia
Orphanet:3283 His bundle tachycardia
Orphanet:3286 Catecholaminergic polymorphic ventricular tachycardia
Orphanet:334 Familial atrial fibrillation
Orphanet:37553 Cardiodysrhythmic potassium-sensitive periodic paralysis
Orphanet:392 Holt-Oram syndrome
Orphanet:45452 Idiopathic neonatal atrial flutter
Orphanet:45453 Incessant infant ventricular tachycardia
Orphanet:51083 Familial short QT syndrome
Orphanet:60041 Congenital heart block
Orphanet:65283 Timothy syndrome
Orphanet:768 Familial long QT syndrome