The search resulted in 106 diseases.
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