Alphabetic Index | Tabular List | Neoplasms | Drugs and Chemicals | Injuries
G71
Primary disorders of muscles
G71.0
Muscular dystrophy
G71.00
Muscular dystrophy, unspecified
G71.01
Duchenne or Becker muscular dystrophy
  • Autosomal recessive, childhood type, muscular dystrophy resembling Duchenne or Becker muscular dystrophy
  • Benign [Becker] muscular dystrophy
  • Severe [Duchenne] muscular dystrophy
G71.02
Facioscapulohumeral muscular dystrophy
  • Scapulohumeral muscular dystrophy
G71.09
Other specified muscular dystrophies
  • 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
  • Limb-girdle muscular dystrophy
  • Ocular muscular dystrophy
  • Oculopharyngeal muscular dystrophy
  • Scapuloperoneal muscular dystrophy
G71.1
Myotonic disorders
G71.11
Myotonic muscular dystrophy
  • Dystrophia myotonica [Steinert]
  • Myotonia atrophica
  • Myotonic dystrophy
  • Proximal myotonic myopathy (PROMM)
  • Steinert disease
G71.12
Myotonia congenita
  • Acetazolamide responsive myotonia congenita
  • Dominant myotonia congenita [Thomsen disease]
  • Myotonia levior
  • Recessive myotonia congenita [Becker disease]
G71.13
Myotonic chondrodystrophy
  • Chondrodystrophic myotonia
  • Congenital myotonic chondrodystrophy
  • Schwartz-Jampel disease
G71.14
Drug induced myotonia
G71.19
Other specified myotonic disorders
  • Myotonia fluctuans
  • Myotonia permanens
  • Neuromyotonia [Isaacs]
  • Paramyotonia congenita (of von Eulenburg)
  • Pseudomyotonia
  • Symptomatic myotonia
G71.2
Congenital myopathies
  • arthrogryposis multiplex congenita (Q74.3)
  • Central core disease
  • Fiber-type disproportion
  • Minicore disease
  • Multicore disease
  • Myotubular (centronuclear) myopathy
  • Nemaline myopathy
G71.3
Mitochondrial myopathy, not elsewhere classified
  • Kearns-Sayre syndrome (H49.81)
  • Leber's disease (H47.21)
  • Leigh's encephalopathy (G31.82)
  • mitochondrial metabolism disorders (E88.4.-)
  • Reye's syndrome (G93.7)
G71.8
Other primary disorders of muscles
G71.9
Primary disorder of muscle, unspecified
  • Hereditary myopathy NOS