| 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 |
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 |
| G71.19 |
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 |