G60.0 ICD 10 Code is a billable and specific code that can be used to indicate a diagnosis of Hereditary motor and sensory neuropathy for reimbursement purposes. The 2023 edition of the American ICD-10-CM code became effective on October 1, 2022.
Terms applicables to G60.0 ICD 10 code
- C - Charcot-Marie-Tooth disease, paralysis or syndrome
- D - Déjérine-Sottas disease or neuropathy (hypertrophic)
- M - Marie-Charcot-Tooth neuropathic muscular atrophy
- R - Roussy-Lévy syndrome
Possible back-references that may be applicable or related to G60.0 ICD10 Code:
- G00-G99 Diseases of the nervous system
- G60-G65 Polyneuropathies and other disorders of the peripheral nervous system
- G60 Hereditary and idiopathic neuropathy
Present On Admission (POA Exempt)
G60.0 ICD 10 code is considered exempt from POA reporting
Clinical information about G60.0 ICD 10 code
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 2,500 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.
Doctors diagnose CMT by doing a neurologic exam, nerve tests, genetic tests, or a nerve biopsy. There is no cure. The disease can be so mild you don't realize you have it or severe enough to make you weak. Physical therapy, occupational therapy, braces and other devices and sometimes surgery can help.
NIH: National Institute of Neurological Disorders and Stroke
The information in this box was provided by MedlinePlus.gov