The search resulted in 106 diseases.
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|---|---|---|---|
| Orphanet:104 | Leber hereditary optic neuropathy | ||
| 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:154 | Familial isolated dilated cardiomyopathy | ||
| 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:206583 | Adult polyglucosan body disease | ||
| Orphanet:2119 | HEC syndrome | ||
| Orphanet:217607 | Familial dilated cardiomyopathy | ||
| Orphanet:217610 | Neuromuscular disease with dilated cardiomyopathy | ||
| Orphanet:217613 | Mitochondrial disease with dilated cardiomyopathy | ||
| Orphanet:217616 | Fatty acid oxidation and ketogenesis disorder with dilated cardiomyopathy | ||
| Orphanet:217619 | Syndrome associated with dilated cardiomyopathy | ||
| Orphanet:217622 | Sensorineural deafness with dilated cardiomyopathy | ||
| Orphanet:217629 | Non-familial dilated cardiomyopathy | ||
| Orphanet:219 | Autosomal recessive limb-girdle muscular dystrophy type 2F | ||
| Orphanet:2229 | Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome | ||
| Orphanet:2331 | Kawasaki disease | ||
| Orphanet:2515 | Microcephaly-cardiomyopathy syndrome | ||
| Orphanet:261 | Emery-Dreifuss muscular dystrophy | ||
| Orphanet:262 | Duchenne and Becker muscular dystrophy | ||
| Orphanet:263494 | DPM3-CDG |