
2015 ICD-9-CM Diagnosis Code 356.1
Peroneal muscular atrophy
- 2015
- Billable Thru Sept 30/2015
- Non-Billable On/After Oct 1/2015
- 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).
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
Clinical Information
- A hereditary motor and sensory neuropathy transmitted most often as an autosomal dominant trait and characterized by progressive distal wasting and loss of reflexes in the muscles of the legs (and occasionally involving the arms). Onset is usually in the second to fourth decade of life. This condition has been divided into two subtypes, hereditary motor and sensory neuropathy (hmsn) types i and ii. Hmsn i is associated with abnormal nerve conduction velocities and nerve hypertrophy, features not seen in hmsn ii. (Adams et al., Principles of Neurology, 6th ed, p1343)
- A progressive hereditary disorder that causes nerve damage
- An inherited degenerative disorder involving the peripheral nerves. It is caused by mutations in the genes that are responsible for the production of proteins necessary for the function and structure of the peripheral nerves. It is characterized by muscle atrophy and weakness in the feet, legs, hands, and arms and loss of sensation in the limbs
- Charcot-marie-tooth disease (cmt) is a group of genetic nerve disorders. It is named after the three doctors who first identified it. In the United States, cmt affects about 1 in 3,300 people. Cmt affects your peripheral nerves. Peripheral nerves carry movement and sensation signals between the brain and spinal cord and the rest of the body. Symptoms usually start around the teen years. Foot problems such as high arches or hammertoes can be early symptoms. As cmt progresses, your lower legs may weaken. Later, your hands may also become weak. There is no cure. The disease can be so mild you don't realize you have it or severe enough to make you weak. Many people with cmt lead active lives and have a normal life span. Physical therapy, occupational therapy, braces and other devices and sometimes surgery can help you cope. genetics home reference
- Group of peripheral nervous system hereditary disorders with varying course, symptoms, neuropathology, and genetics, but generally involving gradual loss of nerve conduction, distal wasting, deformity, and disability
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

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