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Conditions A-Z

A
Anoctaminopathy (LGMD2L)
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B
Becker muscular dystrophy
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Bethlem myopathy
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C
Calpainopathy (LGMD2A)
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Caveolinopathy (LGMD1C)
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Central core disease
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Charcot-Marie-Tooth disease (CMT)
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Congenital fibre type disproportion (CFTD)
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Congenital muscular dystrophy
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Congenital myasthenic syndrome (CMS)
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Congenital myotonic dystrophy
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D
Dermatomyositis (DM)
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Disorders of the neuromuscular junction
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Distal myopathy with rimmed vacuoles (DMRV)
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Duchenne muscular dystrophy (DMD)
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E
Emery-Dreifuss muscular dystrophy
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F
Facioscapulohumeral muscular dystrophy (FSHD)
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Facioscapuloperoneal muscular dystrophy (FSHD)
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G
Glycogen Storage Disease Type V (GSD V)
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GNE myopathy (GNEM)
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H
Hereditary inclusion body myopathy (HIBM)
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Hereditary inclusion body myopathy type 2. (GNEM)
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Hereditary Motor and Sensory Neuropathy (HMSN)
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Hereditary neuropathies
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I
Inclusion body myositis (IBM)
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J
Juvenile dermatomyositis
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L
Limb girdle muscular dystrophies (LGMDs)
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Limb girdle muscular dystrophy 1B (LGMD1B)
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Limb girdle muscular dystrophy 1C (LGMD1C)
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Limb girdle muscular dystrophy 2A (LGMD2A)
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Limb girdle muscular dystrophy 2B (LGMD2B)
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Limb girdle muscular dystrophy 2I (LGMD2I)
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Limb girdle muscular dystrophy 2L (LGMD2L)
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M
Manifesting carriers of Duchenne and Becker muscular dystrophy
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McArdle disease
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Merosin-deficient congenital muscular dystrophy
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Metabolic myopathies
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Minicore (multicore) myopathy
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Mitochondrial myopathy
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Myasthenia gravis
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Myofibrillar myopathies
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Myositis
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Myotonic dystrophy
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Myotubular and other centronuclear myopathies
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N
Nemaline myopathy
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Nonaka myopathy (GNEM)
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O
Oculopharyngeal muscular dystrophy (OPMD)
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P
Periodic paralyses
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Polymyositis (PM) and dermatomyositis (DM)
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Q
Quadriceps-sparing myopathy (QSM)
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S
Sarcoglycanopathies: LGMD2C, LGMD2D, LGMD2E and LGMD2F
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SEPN1-related myopathy
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Spinal muscular atrophy (SMA)
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Steinert’s disease
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U
Ullrich congenital muscular dystrophy
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V
VCP disease
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