Primary disorders of muscles G71
Codes
- • G71.0
Muscular dystrophy - • G71.00 …… 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 …… 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