The search resulted in 55 diseases.
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| Orphanet:1260 | Sino-auricular heart block | ||
| Orphanet:1344 | Atrial standstill | ||
| Orphanet:1369 | Congenital cataract-hypertrophic cardiomyopathy-mitochondrial myopathy syndrome | ||
| Orphanet:154 | Familial isolated dilated cardiomyopathy | ||
| Orphanet:217085 | Mucopolysaccharidosis type 2, severe form | ||
| Orphanet:228012 | Progressive sensorineural hearing loss-hypertrophic cardiomyopathy syndrome | ||
| Orphanet:26791 | Multiple acyl-CoA dehydrogenase deficiency | ||
| Orphanet:273 | Steinert myotonic dystrophy | ||
| Orphanet:319646 | PGM1-CDG | ||
| Orphanet:324 | Fabry disease | ||
| Orphanet:324525 | Hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial DNA mutation | ||
| Orphanet:3282 | Multifocal atrial tachycardia | ||
| Orphanet:329874 | Idiopathic giant cell myocarditis | ||
| Orphanet:3403 | Uhl anomaly | ||
| Orphanet:34217 | Naxos disease | ||
| Orphanet:550 | MELAS | ||
| Orphanet:551 | MERRF | ||
| Orphanet:563 | Peripartum cardiomyopathy | ||
| Orphanet:580 | Mucopolysaccharidosis type 2 | ||
| Orphanet:59306 | McLeod neuroacanthocytosis syndrome | ||
| Orphanet:66529 | Tako-Tsubo cardiomyopathy | ||
| Orphanet:75249 | Familial isolated restrictive cardiomyopathy | ||
| Orphanet:77259 | Gaucher disease type 1 | ||
| Orphanet:77260 | Gaucher disease type 2 | ||
| Orphanet:77261 | Gaucher disease type 3 | ||
| Orphanet:797 | Sarcoidosis | ||
| Orphanet:844 | Atrial tachyarrhythmia with short PR interval | ||
| Orphanet:871 | Familial progressive cardiac conduction defect | ||
| Orphanet:93473 | Hurler syndrome | ||
| Orphanet:93567 | Pediatric systemic sclerosis | ||
| OMIM:115197 | Cardiomyopathy, familial hypertrophic, 4 | ||
| OMIM:115210 | Cardiomyopathy, familial restrictive, 1 | ||
| OMIM:192600 | Cardiomyopathy, familial hypertrophic, 1 | ||
| OMIM:601494 | Cardiomyopathy, dilated, 1D | ||
| OMIM:604401 | Arrhythmogenic right ventricular dysplasia, familial, 6 | ||
| OMIM:607482 | Cardiomyopathy, dilated, 1M | ||
| OMIM:607487 | Cardiomyopathy, hypertrophic, 25 | ||
| OMIM:610193 | Arrhythmogenic right ventricular dysplasia, familial, 10 | ||
| OMIM:611407 | Cardiomyopathy, dilated, 1W | ||
| OMIM:611615 | Cardiomyopathy, dilated, 1X | ||
| OMIM:611878 | Cardiomyopathy, dilated, 1Y | ||
| OMIM:611879 | Cardiomyopathy, dilated, 1Z | ||
| OMIM:611880 | Cardiomyopathy, dilated, 2A | ||
| OMIM:612124 | Cardiomyopathy, familial hypertrophic, 12 | ||
| OMIM:612877 | Cardiomyopathy, dilated, 1BB | ||
| OMIM:613243 | Cardiomyopathy, familial hypertrophic, 13 | ||
| OMIM:613251 | Cardiomyopathy, familial hypertrophic, 14 | ||
| OMIM:613690 | Cardiomyopathy, familial hypertrophic, 7 | ||
| OMIM:613838 | Cardiomyopathy, familial hypertrophic, 16 | ||
| OMIM:613873 | Cardiomyopathy, familial hypertrophic, 17 | ||
| OMIM:615396 | Left ventricular noncompaction 10 | ||
| Orphanet:420429 | Glycogen storage disease due to acid maltase deficiency, late-onset | ||
| Orphanet:436242 | Familial atrial tachyarrhythmia-infra-Hisian cardiac conduction disease | ||
| OMIM:609578 | Cardiomyopathy, familial restrictive 2 | ||
| OMIM:609915 | Cardiomyopathy, dilated, 1Q |