Convert to ICD-10-CM:
356.1 converts approximately to:
- 2015/16 ICD-10-CM G60.0 Hereditary motor and sensory neuropathy
ICD-9-CM Volume 2 Index entries containing back-references to
356.1:
- Atrophy, atrophic
Charcôt-Marie-Tooth 356.1
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

pseudohypertrophic 359.1

spinal (progressive) 335.10

syphilitic 095.6
- Charcôt-Marie-Tooth disease, paralysis, or syndrome 356.1
- Disease, diseased - see also Syndrome
Charcôt-Marie-Tooth 356.1
- Dystrophy, dystrophia 783.9

- Marie-Charcôt-Tooth neuropathic atrophy, muscle 356.1
- Neuropathy, neuropathic (see also Disorder, nerve) 355.9

hypertrophic
Charcôt-Marie-Tooth 356.1
Déjérine-Sottas 356.0

interstitial 356.9

Refsum 356.3
- Paralysis, paralytic (complete) (incomplete) 344.9

Charcôt-Marie-Tooth type 356.1
- Syndrome - see also Disease
Charcôt-Marie-Tooth 356.1