The search resulted in 64 diseases.
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| 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 |