| G71.0 |
Muscular dystrophy
Muscular dystrophy:
autosomal recessive, childhood type, resembling Duchenne or Becker
benign [Becker]
benign scapuloperoneal with early contractures [Emery-Dreifuss]
distal
facioscapulohumeral
limb-girdle
ocular
oculopharyngeal
scapuloperoneal
severe [Duchenne]
Excludes:
- congenital muscular dystrophy:
- NOS ( G71.2 )
- with specific morphological abnormalities of the muscle fibre ( G71.2 )
|
| G71.1 |
Myotonic disorders
Dystrophia myotonica [Steinert]
Myotonia:
chondrodystrophic
drug-induced
symptomatic
Myotonia congenita:
NOS
dominant [Thomsen]
recessive [Becker]
Neuromyotonia [Isaacs]
Paramyotonia congenita
Pseudomyotonia
Use additional external cause code (Chapter XX), if desired, to identify drug, if drug-induced.
|
| G71.2 |
Congenital myopathies
Congenital muscular dystrophy:
NOS
with specific morphological abnormalities of the muscle fibre
Disease:
central core
minicore
multicore
Fibre-type disproportion
Myopathy:
myotubular (centronuclear)
nemaline
|
| G71.3 |
Mitochondrial myopathy, not elsewhere classified
|
| G71.8 |
Other primary disorders of muscles
|
| G71.9 |
Primary disorder of muscle, unspecified
Hereditary myopathy NOS
|