The search resulted in 108 diseases.
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| Orphanet:111 | Barth syndrome | ||
| Orphanet:1344 | Atrial standstill | ||
| Orphanet:1345 | Cardiomyopathy-cataract-hip spine disease | ||
| Orphanet:1359 | Carney complex | ||
| Orphanet:137675 | Histiocytoid cardiomyopathy | ||
| Orphanet:1493 | Vici syndrome | ||
| Orphanet:154 | Familial isolated dilated cardiomyopathy | ||
| Orphanet:158 | Carnitine uptake deficiency | ||
| Orphanet:183 | Eosinophilic granulomatosis with polyangiitis | ||
| Orphanet:2022 | Endomyocardial fibroelastosis | ||
| Orphanet:208600 | Papillary fibroelastoma of the heart | ||
| Orphanet:217093 | Mucopolysaccharidosis type 2, attenuated form | ||
| Orphanet:217622 | Sensorineural deafness with dilated cardiomyopathy | ||
| Orphanet:2331 | Kawasaki disease | ||
| Orphanet:2515 | Microcephaly-cardiomyopathy syndrome | ||
| Orphanet:26791 | Multiple acyl-CoA dehydrogenase deficiency | ||
| Orphanet:289377 | Early-onset myopathy with fatal cardiomyopathy | ||
| Orphanet:300751 | Familial dilated cardiomyopathy with conduction defect due to LMNA mutation | ||
| Orphanet:314637 | Mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency | ||
| Orphanet:324 | Fabry disease | ||
| Orphanet:324410 | X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome | ||
| Orphanet:3282 | Multifocal atrial tachycardia | ||
| Orphanet:3283 | His bundle tachycardia | ||
| Orphanet:329874 | Idiopathic giant cell myocarditis | ||
| Orphanet:3403 | Uhl anomaly | ||
| Orphanet:34217 | Naxos disease | ||
| Orphanet:352563 | Infantile hypertrophic cardiomyopathy due to MRPL44 deficiency | ||
| Orphanet:363618 | LMNA-related cardiocutaneous progeria syndrome | ||
| Orphanet:369913 | Combined oxidative phosphorylation defect type 17 | ||
| Orphanet:45452 | Idiopathic neonatal atrial flutter | ||
| Orphanet:5 | Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency | ||
| Orphanet:54260 | Left ventricular noncompaction | ||
| Orphanet:550 | MELAS | ||
| Orphanet:563 | Peripartum cardiomyopathy | ||
| Orphanet:57777 | Cirrhotic cardiomyopathy | ||
| Orphanet:580 | Mucopolysaccharidosis type 2 | ||
| Orphanet:59306 | McLeod neuroacanthocytosis syndrome | ||
| Orphanet:60041 | Congenital heart block | ||
| Orphanet:615 | Familial atrial myxoma | ||
| Orphanet:64 | Alström syndrome | ||
| Orphanet:65282 | Woolly hair-palmoplantar keratoderma-dilated cardiomyopathy syndrome | ||
| Orphanet:66529 | Tako-Tsubo cardiomyopathy | ||
| Orphanet:66634 | Dilated cardiomyopathy with ataxia | ||
| Orphanet:746 | Mitochondrial trifunctional protein deficiency | ||
| Orphanet:75565 | Tropical endomyocardial fibrosis | ||
| 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:85451 | ATTRV122I amyloidosis | ||
| Orphanet:874 | Adult heart tumor | ||
| Orphanet:90291 | Systemic sclerosis | ||
| Orphanet:93473 | Hurler syndrome | ||
| Orphanet:93476 | Hurler-Scheie syndrome | ||
| Orphanet:93567 | Pediatric systemic sclerosis | ||
| Orphanet:98896 | Duchenne muscular dystrophy | ||
| Orphanet:99901 | Acyl-CoA dehydrogenase 9 deficiency | ||
| OMIM:115197 | Cardiomyopathy, familial hypertrophic, 4 | ||
| OMIM:192600 | Cardiomyopathy, familial hypertrophic, 1 | ||
| OMIM:229300 | Friedreich ataxia 1 | ||
| OMIM:302045 | Cardiomyopathy, dilated, 3B | ||
| OMIM:600858 | Cardiomyopathy, familial hypertrophic, 6 | ||
| OMIM:600884 | Cardiomyopathy, dilated, 1B | ||
| OMIM:601493 | Cardiomyopathy, dilated, 1C | ||
| OMIM:601494 | Cardiomyopathy, dilated, 1D | ||
| OMIM:602086 | Arrhythmogenic right ventricular dysplasia, familial, 3 | ||
| OMIM:604169 | Left ventricular noncompaction 1 | ||
| OMIM:604400 | Arrhythmogenic right ventricular dysplasia, familial, 5 | ||
| OMIM:604765 | Cardiomyopathy, dilated, 1I | ||
| OMIM:606685 | Cardiomyopathy, dilated, 1L | ||
| OMIM:607450 | Arrhythmogenic right ventricular dysplasia, familial, 8 | ||
| OMIM:607482 | Cardiomyopathy, dilated, 1M | ||
| OMIM:608569 | Cardiomyopathy, dilated, 1O | ||
| OMIM:608751 | Cardiomyopathy, familial hypertrophic, 8 | ||
| OMIM:609040 | Arrhythmogenic right ventricular dysplasia, familial, 9 | ||
| OMIM:609909 | Cardiomyopathy, dilated, 1P | ||
| OMIM:610193 | Arrhythmogenic right ventricular dysplasia, familial, 10 | ||
| OMIM:611407 | Cardiomyopathy, dilated, 1W | ||
| OMIM:611528 | Arrhythmogenic right ventricular dysplasia, familial, 12 | ||
| OMIM:611615 | Cardiomyopathy, dilated, 1X | ||
| OMIM:611878 | Cardiomyopathy, dilated, 1Y | ||
| OMIM:611879 | Cardiomyopathy, dilated, 1Z | ||
| OMIM:611880 | Cardiomyopathy, dilated, 2A | ||
| OMIM:612877 | Cardiomyopathy, dilated, 1BB | ||
| OMIM:613122 | Cardiomyopathy, dilated, 1CC | ||
| OMIM:613172 | Cardiomyopathy, dilated, 1DD | ||
| OMIM:613251 | Cardiomyopathy, familial hypertrophic, 14 | ||
| OMIM:613252 | Cardiomyopathy, dilated, 1EE | ||
| OMIM:613286 | Cardiomyopathy, dilated, 1FF | ||
| OMIM:613424 | Cardiomyopathy, dilated, 1R | ||
| OMIM:613426 | Cardiomyopathy, dilated, 1S | ||
| OMIM:613690 | Cardiomyopathy, familial hypertrophic, 7 | ||
| OMIM:613694 | Cardiomyopathy, dilated, 1U | ||
| OMIM:613697 | Cardiomyopathy, dilated, 1V | ||
| OMIM:613740 | Cardiomyopathy, dilated, 1T | ||
| OMIM:613881 | Cardiomyopathy, dilated, 1HH | ||
| OMIM:614672 | Cardiomyopathy, dilated, 2B | ||
| OMIM:614676 | Cardiomyopathy, familial hypertrophic, 21 | ||
| OMIM:615184 | Cardiomyopathy, dilated, 1II | ||
| OMIM:615373 | Left ventricular noncompaction 8 | ||
| OMIM:615396 | Left ventricular noncompaction 10 | ||
| OMIM:609470 | Left ventricular noncompaction 2 | ||
| OMIM:615745 | Atrial standstill 2 | ||
| OMIM:615248 | Cardiomyopathy, dilated, 1KK | ||
| Orphanet:436242 | Familial atrial tachyarrhythmia-infra-Hisian cardiac conduction disease | ||
| OMIM:609915 | Cardiomyopathy, dilated, 1Q | ||
| OMIM:617047 | CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 26 |