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 Charcôt-Marie-Tooth 356.1
  muscle, muscular 728.2 muscle, muscular 728.2   disuse 728.2 disuse 728.2 
  Duchenne-Aran 335.21 Duchenne-Aran 335.21 
  extremity (lower) (upper) 728.2 extremity (lower) (upper) 728.2 
  familial spinal 335.11 familial spinal 335.11 
  general 728.2 general 728.2 
  idiopathic 728.2 idiopathic 728.2 
  infantile spinal 335.0 infantile spinal 335.0 
  myelopathic (progressive) 335.10 myelopathic (progressive) 335.10 
  myotonic 359.2 myotonic 359.2 
  neuritic 356.1 neuritic 356.1
  neuropathic (peroneal) (progressive) 356.1 neuropathic (peroneal) (progressive) 356.1
  peroneal 356.1 peroneal 356.1
  primary (idiopathic) 728.2 primary (idiopathic) 728.2 
  progressive (familial) (hereditary) (pure) 335.21 progressive (familial) (hereditary) (pure) 335.21 
  pseudohypertrophic 359.1 pseudohypertrophic 359.1 
  spinal (progressive) 335.10 spinal (progressive) 335.10 
  syphilitic 095.6 syphilitic 095.6 
 
 
- Charcôt-Marie-Tooth disease, paralysis, or syndrome 356.1
- Disease, diseased - see also Syndrome Charcôt-Marie-Tooth 356.1 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 hypertrophic  Charcôt-Marie-Tooth 356.1 Charcôt-Marie-Tooth 356.1
  Déjérine-Sottas 356.0 Déjérine-Sottas 356.0 
  interstitial 356.9 interstitial 356.9 
  Refsum 356.3 Refsum 356.3 
 
 
- Paralysis, paralytic (complete) (incomplete) 344.9  Charcôt-Marie-Tooth type 356.1 Charcôt-Marie-Tooth type 356.1
 
- Syndrome - see also Disease Charcôt-Marie-Tooth 356.1 Charcôt-Marie-Tooth 356.1