The search resulted in 66 diseases.
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| Orphanet:101016 | Romano-Ward syndrome | ||
| Orphanet:111 | Barth syndrome | ||
| Orphanet:130 | Brugada syndrome | ||
| Orphanet:1344 | Atrial standstill | ||
| Orphanet:1359 | Carney complex | ||
| Orphanet:137675 | Histiocytoid cardiomyopathy | ||
| Orphanet:217601 | Hypertrophic cardiomyopathy due to intensive athletic training | ||
| Orphanet:217622 | Sensorineural deafness with dilated cardiomyopathy | ||
| Orphanet:228140 | Idiopathic ventricular fibrillation, not Brugada type | ||
| Orphanet:264 | Autosomal dominant limb-girdle muscular dystrophy type 1B | ||
| Orphanet:26793 | Very long chain acyl-CoA dehydrogenase deficiency | ||
| Orphanet:300751 | Familial dilated cardiomyopathy with conduction defect due to LMNA mutation | ||
| Orphanet:324 | Fabry disease | ||
| Orphanet:3283 | His bundle tachycardia | ||
| 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:45452 | Idiopathic neonatal atrial flutter | ||
| Orphanet:51083 | Familial short QT syndrome | ||
| Orphanet:550 | MELAS | ||
| Orphanet:563 | Peripartum cardiomyopathy | ||
| Orphanet:65283 | Timothy syndrome | ||
| Orphanet:66529 | Tako-Tsubo cardiomyopathy | ||
| Orphanet:66634 | Dilated cardiomyopathy with ataxia | ||
| Orphanet:768 | Familial long QT syndrome | ||
| Orphanet:797 | Sarcoidosis | ||
| Orphanet:85443 | AL amyloidosis | ||
| Orphanet:871 | Familial progressive cardiac conduction defect | ||
| Orphanet:90647 | Jervell and Lange-Nielsen syndrome | ||
| Orphanet:94062 | Coronary artery disease - hyperlipidemia - hypertension - diabetes - osteoporosis | ||
| Orphanet:98863 | X-linked Emery-Dreifuss muscular dystrophy | ||
| Orphanet:98895 | Becker muscular dystrophy | ||
| Orphanet:98896 | Duchenne muscular dystrophy | ||
| Orphanet:98909 | Desminopathy | ||
| OMIM:115197 | Cardiomyopathy, familial hypertrophic, 4 | ||
| OMIM:192500 | Long QT syndrome 1 | ||
| OMIM:192600 | Cardiomyopathy, familial hypertrophic, 1 | ||
| OMIM:600858 | Cardiomyopathy, familial hypertrophic, 6 | ||
| OMIM:600996 | Arrhythmogenic right ventricular dysplasia, familial, 2 | ||
| OMIM:601493 | Cardiomyopathy, dilated, 1C | ||
| OMIM:601494 | Cardiomyopathy, dilated, 1D | ||
| OMIM:602087 | Arrhythmogenic right ventricular dysplasia, familial, 4 | ||
| OMIM:603830 | Long QT syndrome 3 | ||
| OMIM:604169 | Left ventricular noncompaction 1 | ||
| OMIM:604400 | Arrhythmogenic right ventricular dysplasia, familial, 5 | ||
| OMIM:604401 | Arrhythmogenic right ventricular dysplasia, familial, 6 | ||
| OMIM:606685 | Cardiomyopathy, dilated, 1L | ||
| OMIM:607450 | Arrhythmogenic right ventricular dysplasia, familial, 8 | ||
| OMIM:608751 | Cardiomyopathy, familial hypertrophic, 8 | ||
| 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:611819 | Long QT syndrome 10 | ||
| OMIM:612124 | Cardiomyopathy, familial hypertrophic, 12 | ||
| OMIM:613172 | Cardiomyopathy, dilated, 1DD | ||
| OMIM:613688 | Long QT syndrome 2 | ||
| OMIM:613690 | Cardiomyopathy, familial hypertrophic, 7 | ||
| OMIM:613765 | Cardiomyopathy, familial hypertrophic, 9 | ||
| OMIM:614676 | Cardiomyopathy, familial hypertrophic, 21 | ||
| Orphanet:155 | Familial isolated hypertrophic cardiomyopathy | ||
| OMIM:609470 | Left ventricular noncompaction 2 | ||
| OMIM:615821 | Cardiomyopathy, dilated, with woolly hair, keratoderma, and toothagenesis | ||
| OMIM:617047 | CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 26 |