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2014 ICD-9-CM Diagnosis Code 356.1
Peroneal muscular atrophy
- 2014
- Billable Thru Sept 30/2015
- Non-Billable On/After Oct 1/2015
- Short description: Peroneal muscle atrophy.
- ICD-9-CM 356.1 is a billable medical code that can be used to indicate a diagnosis on a reimbursement claim, however, 356.1 should only be used for claims with a date of service on or before September 30, 2015. For claims with a date of service on or after October 1, 2015, use an equivalent ICD-10-CM code (or codes).
- You are viewing the 2014 version of ICD-9-CM 356.1.
- More recent version(s) of ICD-9-CM 356.1: 2015.
Convert to ICD-10-CM:
356.1 converts approximately to:
- 2015/16 ICD-10-CM G60.0 Hereditary motor and sensory neuropathy
Approximate Synonyms
- Charcot Marie Tooth disease
- Charcot Marie Tooth disease type 1
- Charcot Marie Tooth disease type 2
- Charcot Marie Tooth disease type 3
- Charcot Marie Tooth disease type 4
- Charcot Marie Tooth disease, Type 1
- Charcot Marie Tooth disease, Type 2
- Charcot Marie Tooth disease, Type 3
- Charcot Marie Tooth disease, Type 4
- Charcot-Marie-Tooth disease
- Charcot-Marie-Tooth disease type 4
- Charcot-Marie-Tooth disease, type 3
- Charcot-Marie-Tooth disease, type I
- Charcot-Marie-Tooth disease, type II
Applies To
- Charcot-Marie-Tooth disease
- Neuropathic muscular atrophy
ICD-9-CM Volume 2 Index entries containing back-references to
356.1:
- Atrophy, atrophic
Charcôt-Marie-Tooth 356.1
muscle, muscular 728.2![](/images/note.png)
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disuse 728.2![](/images/note.png)
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Duchenne-Aran 335.21![](/images/note.png)
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extremity (lower) (upper) 728.2![](/images/note.png)
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familial spinal 335.11![](/images/note.png)
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general 728.2![](/images/note.png)
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idiopathic 728.2![](/images/note.png)
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infantile spinal 335.0![](/images/note.png)
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myelopathic (progressive) 335.10![](/images/note.png)
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myotonic 359.21![](/images/note.png)
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neuritic 356.1![](/images/16x16.gif)
neuropathic (peroneal) (progressive) 356.1![](/images/16x16.gif)
peroneal 356.1![](/images/16x16.gif)
primary (idiopathic) 728.2![](/images/note.png)
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progressive (familial) (hereditary) (pure) 335.21![](/images/note.png)
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pseudohypertrophic 359.1![](/images/note.png)
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spinal (progressive) 335.10![](/images/note.png)
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syphilitic 095.6![](/images/note.png)
- Charcôt-Marie-Tooth disease, paralysis, or syndrome 356.1
- Disease, diseased - see also Syndrome
Charcôt-Marie-Tooth 356.1
- Dystrophy, dystrophia 783.9
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- Marie-Charcôt-Tooth neuropathic atrophy, muscle 356.1
- Neuropathy, neuropathic (see also Disorder, nerve) 355.9
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hypertrophic![](/images/16x16.gif)
Charcôt-Marie-Tooth 356.1![](/images/16x16.gif)
Déjérine-Sottas 356.0![](/images/note.png)
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interstitial 356.9![](/images/note.png)
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Refsum 356.3![](/images/note.png)
- Paralysis, paralytic (complete) (incomplete) 344.9
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Charcôt-Marie-Tooth type 356.1
- Syndrome - see also Disease
Charcôt-Marie-Tooth 356.1