Conditions A-Z
B
C
Calpainopathy (LGMD2A)
Details
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)
Details
F
G
H
Hereditary inclusion body myopathy (HIBM)
Details
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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L
Limb girdle muscular dystrophies (LGMDs)
Details
Limb girdle muscular dystrophy 1B (LGMD1B)
Details
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)
Details
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
Details
N
P
S
Sarcoglycanopathies: LGMD2C, LGMD2D, LGMD2E and LGMD2F
Details
SEPN1-related myopathy
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Spinal muscular atrophy (SMA)
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Steinert’s disease
Details