The search resulted in 61 diseases.
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| Orphanet:101016 | Romano-Ward syndrome | ||
| Orphanet:1260 | Sino-auricular heart block | ||
| Orphanet:130 | Brugada syndrome | ||
| Orphanet:1344 | Atrial standstill | ||
| Orphanet:137625 | Glycogen storage disease due to muscle and heart glycogen synthase deficiency | ||
| Orphanet:154 | Familial isolated dilated cardiomyopathy | ||
| Orphanet:166282 | Familial sick sinus syndrome | ||
| Orphanet:208600 | Papillary fibroelastoma of the heart | ||
| Orphanet:217656 | Familial isolated arrhythmogenic right ventricular dysplasia | ||
| Orphanet:228012 | Progressive sensorineural hearing loss-hypertrophic cardiomyopathy syndrome | ||
| Orphanet:228140 | Idiopathic ventricular fibrillation, not Brugada type | ||
| Orphanet:314701 | Primary systemic amyloidosis | ||
| Orphanet:324 | Fabry disease | ||
| Orphanet:324321 | Sinoatrial node dysfunction and deafness | ||
| 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:45453 | Incessant infant ventricular tachycardia | ||
| Orphanet:51083 | Familial short QT syndrome | ||
| Orphanet:54260 | Left ventricular noncompaction | ||
| Orphanet:563 | Peripartum cardiomyopathy | ||
| Orphanet:615 | Familial atrial myxoma | ||
| Orphanet:65283 | Timothy syndrome | ||
| Orphanet:66529 | Tako-Tsubo cardiomyopathy | ||
| Orphanet:768 | Familial long QT syndrome | ||
| Orphanet:77259 | Gaucher disease type 1 | ||
| Orphanet:77260 | Gaucher disease type 2 | ||
| Orphanet:77261 | Gaucher disease type 3 | ||
| Orphanet:797 | Sarcoidosis | ||
| Orphanet:85443 | AL amyloidosis | ||
| Orphanet:871 | Familial progressive cardiac conduction defect | ||
| Orphanet:90647 | Jervell and Lange-Nielsen syndrome | ||
| OMIM:115197 | Cardiomyopathy, familial hypertrophic, 4 | ||
| OMIM:115210 | Cardiomyopathy, familial restrictive, 1 | ||
| OMIM:192500 | Long QT syndrome 1 | ||
| OMIM:192600 | Cardiomyopathy, familial hypertrophic, 1 | ||
| OMIM:601154 | Cardiomyopathy, dilated, 1E | ||
| OMIM:602086 | Arrhythmogenic right ventricular dysplasia, familial, 3 | ||
| OMIM:602087 | Arrhythmogenic right ventricular dysplasia, familial, 4 | ||
| OMIM:603830 | Long QT syndrome 3 | ||
| OMIM:604400 | Arrhythmogenic right ventricular dysplasia, familial, 5 | ||
| OMIM:604401 | Arrhythmogenic right ventricular dysplasia, familial, 6 | ||
| OMIM:607554 | Atrial fibrillation, familial, 3 | ||
| 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:611528 | Arrhythmogenic right ventricular dysplasia, familial, 12 | ||
| OMIM:613243 | Cardiomyopathy, familial hypertrophic, 13 | ||
| OMIM:613251 | Cardiomyopathy, familial hypertrophic, 14 | ||
| OMIM:613424 | Cardiomyopathy, dilated, 1R | ||
| OMIM:613688 | Long QT syndrome 2 | ||
| OMIM:613694 | Cardiomyopathy, dilated, 1U | ||
| OMIM:613697 | Cardiomyopathy, dilated, 1V | ||
| OMIM:613838 | Cardiomyopathy, familial hypertrophic, 16 | ||
| OMIM:615396 | Left ventricular noncompaction 10 | ||
| OMIM:615616 | Arrhythmogenic right ventricular dysplasia, familial, 13 | ||
| OMIM:615745 | Atrial standstill 2 | ||
| OMIM:108770 | Atrial standstill 1 |