The search resulted in 90 diseases.
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| Orphanet:111 | Barth syndrome | ||
| Orphanet:119 | Autosomal recessive limb-girdle muscular dystrophy type 2E | ||
| Orphanet:1345 | Cardiomyopathy-cataract-hip spine disease | ||
| Orphanet:137675 | Histiocytoid cardiomyopathy | ||
| Orphanet:1493 | Vici syndrome | ||
| Orphanet:158 | Carnitine uptake deficiency | ||
| Orphanet:1606 | 1p36 deletion syndrome | ||
| Orphanet:168796 | Heart-hand syndrome, Slovenian type | ||
| Orphanet:183 | Eosinophilic granulomatosis with polyangiitis | ||
| Orphanet:2022 | Endomyocardial fibroelastosis | ||
| Orphanet:206546 | Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers | ||
| Orphanet:206554 | Autosomal recessive limb-girdle muscular dystrophy type 2M | ||
| Orphanet:217622 | Sensorineural deafness with dilated cardiomyopathy | ||
| Orphanet:219 | Autosomal recessive limb-girdle muscular dystrophy type 2F | ||
| Orphanet:2229 | Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome | ||
| Orphanet:2515 | Microcephaly-cardiomyopathy syndrome | ||
| Orphanet:263494 | DPM3-CDG | ||
| Orphanet:264 | Autosomal dominant limb-girdle muscular dystrophy type 1B | ||
| Orphanet:26791 | Multiple acyl-CoA dehydrogenase deficiency | ||
| Orphanet:273 | Steinert myotonic dystrophy | ||
| Orphanet:289377 | Early-onset myopathy with fatal cardiomyopathy | ||
| Orphanet:300751 | Familial dilated cardiomyopathy with conduction defect due to LMNA mutation | ||
| Orphanet:314701 | Primary systemic amyloidosis | ||
| Orphanet:319646 | PGM1-CDG | ||
| Orphanet:3283 | His bundle tachycardia | ||
| Orphanet:329874 | Idiopathic giant cell myocarditis | ||
| Orphanet:334 | Familial atrial fibrillation | ||
| Orphanet:34217 | Naxos disease | ||
| Orphanet:34587 | Glycogen storage disease due to LAMP-2 deficiency | ||
| Orphanet:367 | Glycogen storage disease due to glycogen branching enzyme deficiency | ||
| Orphanet:369913 | Combined oxidative phosphorylation defect type 17 | ||
| Orphanet:37553 | Cardiodysrhythmic potassium-sensitive periodic paralysis | ||
| Orphanet:5 | Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency | ||
| Orphanet:550 | MELAS | ||
| Orphanet:563 | Peripartum cardiomyopathy | ||
| Orphanet:59306 | McLeod neuroacanthocytosis syndrome | ||
| Orphanet:64 | Alström syndrome | ||
| Orphanet:65282 | Woolly hair-palmoplantar keratoderma-dilated cardiomyopathy syndrome | ||
| Orphanet:66634 | Dilated cardiomyopathy with ataxia | ||
| Orphanet:73224 | Tubular renal disease-cardiomyopathy syndrome | ||
| Orphanet:746 | Mitochondrial trifunctional protein deficiency | ||
| Orphanet:79159 | Isobutyryl-CoA dehydrogenase deficiency | ||
| Orphanet:85443 | AL amyloidosis | ||
| Orphanet:91131 | DK1-CDG | ||
| Orphanet:98863 | X-linked Emery-Dreifuss muscular dystrophy | ||
| Orphanet:98895 | Becker muscular dystrophy | ||
| Orphanet:98896 | Duchenne muscular dystrophy | ||
| Orphanet:98909 | Desminopathy | ||
| Orphanet:99901 | Acyl-CoA dehydrogenase 9 deficiency | ||
| OMIM:145350 | Hypertaurinuric cardiomyopathy | ||
| OMIM:229300 | Friedreich ataxia 1 | ||
| OMIM:302045 | Cardiomyopathy, dilated, 3B | ||
| OMIM:600884 | Cardiomyopathy, dilated, 1B | ||
| OMIM:601154 | Cardiomyopathy, dilated, 1E | ||
| OMIM:601494 | Cardiomyopathy, dilated, 1D | ||
| OMIM:604145 | Cardiomyopathy, dilated, 1G | ||
| OMIM:604765 | Cardiomyopathy, dilated, 1I | ||
| OMIM:606685 | Cardiomyopathy, dilated, 1L | ||
| OMIM:607482 | Cardiomyopathy, dilated, 1M | ||
| OMIM:608569 | Cardiomyopathy, dilated, 1O | ||
| OMIM:609909 | Cardiomyopathy, dilated, 1P | ||
| 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:612158 | Cardiomyopathy, dilated, 1AA with or without left ventricular noncompaction | ||
| OMIM:612877 | Cardiomyopathy, dilated, 1BB | ||
| OMIM:613122 | Cardiomyopathy, dilated, 1CC | ||
| OMIM:613172 | Cardiomyopathy, dilated, 1DD | ||
| OMIM:613252 | Cardiomyopathy, dilated, 1EE | ||
| OMIM:613286 | Cardiomyopathy, dilated, 1FF | ||
| OMIM:613424 | Cardiomyopathy, dilated, 1R | ||
| OMIM:613642 | Cardiomyopathy, dilated, 1GG | ||
| OMIM:613694 | Cardiomyopathy, dilated, 1U | ||
| OMIM:613697 | Cardiomyopathy, dilated, 1V | ||
| OMIM:613740 | Cardiomyopathy, dilated, 1T | ||
| OMIM:613765 | Cardiomyopathy, familial hypertrophic, 9 | ||
| OMIM:614672 | Cardiomyopathy, dilated, 2B | ||
| OMIM:615184 | Cardiomyopathy, dilated, 1II | ||
| OMIM:615235 | Cardiomyopathy, dilated, 1JJ | ||
| OMIM:615396 | Left ventricular noncompaction 10 | ||
| OMIM:615745 | Atrial standstill 2 | ||
| OMIM:615821 | Cardiomyopathy, dilated, with woolly hair, keratoderma, and toothagenesis | ||
| OMIM:615916 | Cardiomyopathy, dilated, 1nn | ||
| OMIM:615248 | Cardiomyopathy, dilated, 1KK | ||
| Orphanet:436242 | Familial atrial tachyarrhythmia-infra-Hisian cardiac conduction disease | ||
| OMIM:604288 | Cardiomyopathy, dilated, 1H | ||
| OMIM:605582 | Cardiomyopathy, dilated, 1K | ||
| OMIM:609915 | Cardiomyopathy, dilated, 1Q |