G71.- Primary disorders of muscles


  • Arthrogryposis multiplex congenita (Q74.3)
  • Metabolic disorders (E70-E88)
  • Myositis (M60.-)
  • G71
  • Primary disorders of muscles
    • G71.0
    Muscular dystrophy
      • G71.00
    Muscular dystrophy, unspecified
      • G71.01
    Duchenne or Becker muscular dystrophy
      • G71.02
    Facioscapulohumeral muscular dystrophy
      • G71.09
    Other specified muscular dystrophies
    • G71.1
    Myotonic disorders
      • G71.11
    Myotonic muscular dystrophy
      • G71.12
    Myotonia congenita
      • G71.13
    Myotonic chondrodystrophy
      • G71.14
    Drug induced myotonia
      • G71.19
    Other specified myotonic disorders
    • G71.2
    Congenital myopathies
      • G71.20
    Congenital myopathy, unspecified
      • G71.21
    Nemaline myopathy
      • G71.22
    Centronuclear myopathy
          • G71.220
    X-linked myotubular myopathy
          • G71.228
    Other centronuclear myopathy
      • G71.29
    Other congenital myopathy
    • G71.3
    Mitochondrial myopathy, not elsewhere classified
    • G71.8
    Other primary disorders of muscles
    • G71.9
    Primary disorder of muscle, unspecified