Primary disorders of muscles (G71)

Diseases of the nervous system
- Diseases of myoneural junction and muscle (G70-G73)
  - - 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
    - G71.03 - Limb girdle muscular dystrophies
    - G71.031 - Autosomal dominant limb girdle muscular dystrophy
    - G71.032 - Autosom recess limb girdle musc dyst d/t calpain-3 dysfnct
    - G71.033 - Limb girdle muscular dystrophy due to dysferlin dysfunction
    - G71.034 - Limb girdle musc dyst due to sarcoglycan dysfunction
    - G71.0340 - Limb girdle musc dyst due to sarcoglycan dysfnct, unsp
    - G71.0341 - Limb girdle musc dyst due to alpha sarcoglycan dysfunction
    - G71.0342 - Limb girdle musc dyst due to beta sarcoglycan dysfunction
    - G71.0349 - Limb girdle musc dyst due to other sarcoglycan dysfunction
    - G71.035 - Limb girdle musc dyst due to anoctamin-5 dysfunction
    - G71.038 - Other limb girdle muscular dystrophy
    - G71.039 - Limb girdle muscular dystrophy, unspecified
    - 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

Diseases of the nervous system