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2009 ICD-9-CM

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Atrophy, atrophic
striated 095.8
muscle, muscular 728.2
disuse 728.2
Duchenne-Aran 335.21
extremity (lower) (upper) 728.2
familial spinal 335.11
general 728.2
idiopathic 728.2
infantile spinal 335.0
myelopathic (progressive) 335.10
myotonic 359.21
neuritic 356.1
neuropathic (peroneal) (progressive) 356.1
peroneal 356.1
primary (idiopathic) 728.2
progressive (familial) (hereditary) (pure) 335.21
adult (spinal) 335.19
infantile (spinal) 335.0
juvenile (spinal) 335.11
spinal 335.10
adult 335.19
hereditary or familial 335.11
infantile 335.0
pseudohypertrophic 359.1
spinal (progressive) 335.10
adult 335.19
Aran-Duchenne 335.21
familial 335.11
hereditary 335.11
infantile 335.0
juvenile 335.11
syphilitic 095.6
myocardium (see also Degeneration, myocardial) 429.1
myometrium (senile) 621.8
cervix 622.8
myotatic 728.2
myotonia 359.21
nail 703.8
congenital 757.5
nasopharynx 472.2
nerve - see also Disorder, nerve
abducens 378.54
accessory 352.4
acoustic or auditory 388.5
cranial 352.9
first (olfactory) 352.0
second (optic) (see also Atrophy, optic nerve) 377.10
third (oculomotor) (partial) 378.51
total 378.52
fourth (trochlear) 378.53
 
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