Alpha-crystallinopathy
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(Orphanet:98910)
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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 1F
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(Orphanet:55595)
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Autosomal recessive centronuclear myopathy
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(Orphanet:169186)
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Autosomal recessive limb-girdle muscular dystrophy type 2B
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(Orphanet:268)
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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 2J
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(Orphanet:140922)
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Autosomal recessive limb-girdle muscular dystrophy type 2L
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(Orphanet:206549)
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Autosomal recessive progressive external ophthalmoplegia
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(Orphanet:254886)
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Distal myopathy with early respiratory muscle involvement
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(Orphanet:34521)
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Glycogen storage disease due to LAMP-2 deficiency
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(Orphanet:34587)
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INCLUSION BODY MYOPATHY 2, AUTOSOMAL RECESSIVE
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(OMIM:600737)
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MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION),TYPE B, 6
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(OMIM:608840)
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MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUTMENTAL RETARDATION), TYPE B, 5
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(OMIM:606612)
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MYOPATHY, DISTAL, 3
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(OMIM:610099)
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MYOPATHY, HYALINE BODY, AUTOSOMAL RECESSIVE
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(OMIM:255160)
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Marinesco-Sjögren syndrome
|
(Orphanet:559)
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Mitochondrial DNA depletion syndrome, myopathic form
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(Orphanet:254875)
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Myopathy and diabetes mellitus
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(Orphanet:2596)
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NEMALINE MYOPATHY 1
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(OMIM:609284)
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NEMALINE MYOPATHY 6
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(OMIM:609273)
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NONAKA MYOPATHY
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(OMIM:605820)
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PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 1
|
(OMIM:157640)
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PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 2
|
(OMIM:609283)
|
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 3
|
(OMIM:609286)
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ZASP-related myofibrillar myopathy
|
(Orphanet:98912)
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