Primary disorders of muscles - G71
Type 2 Excludes
- arthrogryposis multiplex congenita (Q74.3)
- metabolic disorders (E70-E88)
- myositis (M60.-)
Codes
- 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 - Autosomal recessive limb girdle muscular dystrophy due to calpain-3 dysfunction
- G71.033 - Limb girdle muscular dystrophy due to dysferlin dysfunction
- G71.034 - Limb girdle muscular dystrophy due to sarcoglycan dysfunction
- G71.0340 - Limb girdle muscular dystrophy due to sarcoglycan dysfunction, unspecified
- G71.0341 - Limb girdle muscular dystrophy due to alpha sarcoglycan dysfunction
- G71.0342 - Limb girdle muscular dystrophy due to beta sarcoglycan dysfunction
- G71.0349 - Limb girdle muscular dystrophy due to other sarcoglycan dysfunction
- G71.035 - Limb girdle muscular dystrophy 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
