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Conditions A-Z

B
Becker muscular dystrophy (BMD)
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Bethlem myopathy
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C
Central core disease (CCD)
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Centronuclear and myotubular myopathies
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Charcot-Marie-Tooth disease (CMT)
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Congenital muscular dystrophies (CMD)
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Congenital myasthenic syndromes (CMS)
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Congenital myopathy with fibre type disproportion (CFTD)
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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 myopathies
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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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G
GNE myopathy
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I
Inclusion body myositis (IBM)
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J
Juvenile dermatomyositis
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L
LAMA2-related muscular dystrophies (LAMA2-RDs)
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Limb girdle muscular dystrophy (LGMD) General
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Limb girdle muscular dystrophy R1 (LGMDR1) Previous name: LGMD2A
Read Limb girdle muscular dystrophy R1 (LGMDR1) Previous name: LGMD2A
Limb girdle muscular dystrophy R2 (LGMDR2) Previous name: LGMD2B
Read Limb girdle muscular dystrophy R2 (LGMDR2) Previous name: LGMD2B
Limb girdle muscular dystrophy R9 (LGMDR9) Previous name: LGMD2I
Read Limb girdle muscular dystrophy R9 (LGMDR9) Previous name: LGMD2I
Limb girdle muscular dystrophy sarcoglycanopathies (LGMDR3, LGMDR4, LGMDR5, LGMDR6) Previous names: LGMD2D, LGMD2E, LGMD2C, LGMD2F
Read Limb girdle muscular dystrophy sarcoglycanopathies (LGMDR3, LGMDR4, LGMDR5, LGMDR6) Previous names: LGMD2D, LGMD2E, LGMD2C, LGMD2F
LMNA-related congenital muscular dystrophy (L-CMD)
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M
Manifesting carriers of Duchenne and Becker muscular dystrophy
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McArdle disease
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Mitochondrial disease
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Multiminicore disease (MmD)
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Myasthenia gravis (MG)
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Myofibrillar myopathies (MFM)
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Myotonic dystrophy type 1 (DM1)
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Myotonic dystrophy type 2 (DM2)
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N
Nemaline myopathy (NM)
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Non-dystrophic myotonias (NDM)
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O
Oculopharyngeal muscular dystrophy (OPMD)
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P
Periodic paralysis (PP)
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Polymyositis (PM)
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Pompe disease
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S
SELENON-related myopathy (SELENON-RM)
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Spinal muscular atrophy (SMA)
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U
Ullrich congenital muscular dystrophy (UCMD)
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