Autosomal recessive, childhood type, muscular dystrophy resembling Duchenne or Becker muscular dystrophy

Benign [Becker] muscular dystrophy

Severe [Duchenne] muscular dystrophy

Scapulohumeral muscular dystrophy

LGMD D4 calpain-3-related

LGMD D5 collagen 6-related

Limb girdle muscular dystrophy type 1

Limb girdle muscular dystrophy type 2A

LGMD R1 calpain-3-related

Primary calpainopathy

Dysferlinopathy

LGMD R2 dysferlin-related

Limb girdle muscular dystrophy type 2B

Miyoshi Myopathy type 1

Sarcoglycanopathy, NOS

Alpha sarcoglycanopathy

Limb-girdle muscular dystrophy due to alpha-sarcoglycan deficiency

Limb girdle muscular dystrophy type 2D

Beta sarcoglycanopathy

Limb girdle muscular dystrophy due to beta-sarcoglycan deficiency

Limb girdle muscular dystrophy type 2E

Delta sarcoglycanopathy

Delta-sarcoglycan-related LGMD R6

Gamma sarcoglycanopathy

Gamma-sarcoglycan-related LGMD R5

Limb girdle muscular dystrophy type 2C

Limb girdle muscular dystrophy type 2F

Anoctamin-5-related LGMD R12

Anoctaminopathy

Autosomal recessive limb girdle muscular dystrophy type 2L

Miyoshi myopathy type 3

LGMD R9 FKRP-related

LGMD R22 collagen 6-related

Limb girdle muscular dystrophy due to fukutin related protein dysfunction

Limb girdle muscular dystrophy type 2I

Other autosomal recessive limb girdle muscular dystrophy

Benign scapuloperoneal muscular dystrophy with early contractures [Emery-Dreifuss]

Congenital muscular dystrophy NOS

Congenital muscular dystrophy with specific morphological abnormalities of the muscle fiber

Distal muscular dystrophy

Ocular muscular dystrophy

Oculopharyngeal muscular dystrophy

Scapuloperoneal muscular dystrophy

Dystrophia myotonica [Steinert]

Myotonia atrophica

Myotonic dystrophy

Proximal myotonic myopathy (PROMM)

Steinert disease

Acetazolamide responsive myotonia congenita

Dominant myotonia congenita [Thomsen disease]

Myotonia levior

Recessive myotonia congenita [Becker disease]

Chondrodystrophic myotonia

Congenital myotonic chondrodystrophy

Schwartz-Jampel disease

Myotonia fluctuans

Myotonia permanens

Neuromyotonia [Isaacs]

Paramyotonia congenita (of von Eulenburg)

Pseudomyotonia

Symptomatic myotonia

Myotubular (centronuclear) myopathy

Autosomal centronuclear myopathy

Autosomal dominant centronuclear myopathy

Autosomal recessive centronuclear myopathy

Centronuclear myopathy, NOS

Central core disease

Minicore disease

Multicore disease

Multiminicore disease

Hereditary myopathy NOS