Autosomal dominant Emery-Dreifuss muscular dystrophy
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(Orphanet:98853)
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Autosomal dominant limb-girdle muscular dystrophy type 1A
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(Orphanet:266)
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Autosomal dominant limb-girdle muscular dystrophy type 1B
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(Orphanet:264)
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Autosomal dominant limb-girdle muscular dystrophy type 1D
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(Orphanet:34516)
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Autosomal dominant limb-girdle muscular dystrophy type 1F
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(Orphanet:55595)
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Autosomal dominant limb-girdle muscular dystrophy type 1G
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(Orphanet:55596)
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Autosomal recessive Emery-Dreifuss muscular dystrophy
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(Orphanet:98855)
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Autosomal recessive limb-girdle muscular dystrophy type 2H
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(Orphanet:1878)
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Autosomal recessive limb-girdle muscular dystrophy type 2I
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(Orphanet:34515)
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Autosomal recessive limb-girdle muscular dystrophy type 2L
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(Orphanet:206549)
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Congenital muscular dystrophy type 1B
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(Orphanet:98893)
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Congenital muscular dystrophy with cerebellar involvement
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(Orphanet:370959)
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Distal myopathy with early respiratory muscle involvement
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(Orphanet:34521)
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Distal myopathy with vocal cord weakness
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(Orphanet:600)
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Duchenne muscular dystrophy
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(Orphanet:98896)
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Facioscapulohumeral dystrophy
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(Orphanet:269)
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Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
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(Orphanet:52430)
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MUSCULAR DYSTROPHY, CONGENITAL, MEROSIN-POSITIVE
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(OMIM:609456)
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MUSCULAR DYSTROPHY, PROGRESSIVE PECTORODORSAL
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(OMIM:310095)
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Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers
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(Orphanet:206546)
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VACUOLAR NEUROMYOPATHY
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(OMIM:601846)
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