ICD-10 Diagnosis Code G60.0

Hereditary motor and sensory neuropathy

Diagnosis Code G60.0

ICD-10: G60.0
Short Description: Hereditary motor and sensory neuropathy
Long Description: Hereditary motor and sensory neuropathy
This is the 2018 version of the ICD-10-CM diagnosis code G60.0

Valid for Submission
The code G60.0 is valid for submission for HIPAA-covered transactions.

Code Classification
  • Diseases of the nervous system (G00–G99)
    • Polyneuropathies and other disorders of the peripheral nervous system (G60-G65)
      • Hereditary and idiopathic neuropathy (G60)

Information for Medical Professionals

Convert to ICD-9 Additional informationCallout TooltipGeneral Equivalence Map
The ICD-10 and ICD-9 GEMs are used to facilitate linking between the diagnosis codes in ICD-9-CM and the new ICD-10-CM code set. The GEMs are the raw material from which providers, health information vendors and payers can derive specific applied mappings to meet their needs.

  • Charcot-Marie-Tooth disease, type I
  • Charcot-Marie-Tooth disease, type IA
  • Charcot-Marie-Tooth disease, type IB
  • Charcot-Marie-Tooth disease, type IC
  • Charcot-Marie-Tooth disease, type II
  • Congenital paraplegia
  • Déjérine-Sottas disease
  • Hereditary hypertrophic neuropathy with paraproteinemia
  • Hereditary liability to pressure palsies
  • Hereditary motor and sensory neuropathy
  • Hereditary motor and sensory neuropathy with optic atrophy
  • Hereditary motor and sensory neuropathy with retinitis pigmentosa
  • Hereditary optic atrophy
  • Hereditary sensory and autonomic neuropathy
  • Hereditary sensory and autonomic neuropathy
  • Hereditary sensory and autonomic neuropathy type I
  • Hereditary sensory and autonomic neuropathy type II
  • Hereditary sensory-motor neuropathy, type V
  • Hereditary spastic paraplegia
  • Hypertrophic interstitial neuropathy
  • Primary optic atrophy
  • Roussy-Lévy syndrome
  • Spastic paraplegia
  • X-linked hereditary motor and sensory neuropathy

Index of Diseases and Injuries
References found for the code G60.0 in the Index of Diseases and Injuries:

Information for Patients

Charcot-Marie-Tooth Disease

Also called: Hereditary motor and sensory neuropathy, Peroneal muscular atrophy

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

  • Charcot-Marie-Tooth disease (Medical Encyclopedia)

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Charcot-Marie-Tooth disease Charcot-Marie-Tooth disease is a group of progressive disorders that affect the peripheral nerves. Peripheral nerves connect the brain and spinal cord to muscles and to sensory cells that detect sensations such as touch, pain, heat, and sound. Damage to the peripheral nerves can result in loss of sensation and wasting (atrophy) of muscles in the feet, legs, and hands.Charcot-Marie-Tooth disease usually becomes apparent in adolescence or early adulthood, but onset may occur anytime from early childhood through late adulthood. Symptoms of Charcot-Marie-Tooth disease vary in severity, even among members of the same family. Some people never realize they have the disorder, but most have a moderate amount of physical disability. A small percentage of people experience severe weakness or other problems which, in rare cases, can be life-threatening. In most affected individuals, however, Charcot-Marie-Tooth disease does not affect life expectancy.Typically, the earliest symptoms of Charcot-Marie-Tooth disease involve balance difficulties, clumsiness, and muscle weakness in the feet. Affected individuals may have foot abnormalities such as high arches (pes cavus), flat feet (pes planus), or curled toes (hammer toes). They often have difficulty flexing the foot or walking on the heel of the foot. These difficulties may cause a higher than normal step (or gait) and increase the risk of ankle injuries and tripping.As the disease progresses, muscles in the lower legs usually weaken, but leg and foot problems rarely require the use of a wheelchair. Affected individuals may also develop weakness in the hands, causing difficulty with daily activities such as writing, fastening buttons, and turning doorknobs. People with this disorder typically experience a decreased sensitivity to touch, heat, and cold in the feet and lower legs, but occasionally feel aching or burning sensations. In some cases, affected individuals experience gradual hearing loss, deafness, or loss of vision.There are several types of Charcot-Marie-Tooth disease. Type 1 Charcot-Marie-Tooth disease (CMT1) is characterized by abnormalities in myelin, the fatty substance that covers nerve cells, protecting them and helping to conduct nerve impulses. These abnormalities slow the transmission of nerve impulses. Type 2 Charcot-Marie-Tooth disease (CMT2) is characterized by abnormalities in the fiber, or axon, that extends from a nerve cell body and transmits nerve impulses. These abnormalities reduce the strength of the nerve impulse. Type 4 Charcot-Marie-Tooth disease (CMT4) affects either the axon or myelin and is distinguished from the other types by its pattern of inheritance. In intermediate forms of Charcot-Marie-Tooth disease, the nerve impulses are both slowed and reduced in strength, probably due to abnormalities in both axons and myelin. Type X Charcot-Marie-Tooth disease (CMTX) is caused by mutations in a gene on the X chromosome, one of the two sex chromosomes. Within the various types of Charcot-Marie-Tooth disease, subtypes (such as CMT1A, CMT1B, CMT2A, CMT4A, and CMTX1) are distinguished by the specific gene that is altered.Sometimes other, more historical names are used to describe this disorder. For example, Roussy-Levy syndrome is a form of Charcot-Marie-Tooth disease defined by the additional feature of rhythmic shaking (tremors). Dejerine-Sottas syndrome is a term sometimes used to describe a severe, early childhood form of Charcot-Marie-Tooth disease; it is also sometimes called Charcot-Marie-Tooth disease type 3 (CMT3). Depending on the specific gene that is altered, this severe, early onset form of the disorder may also be classified as CMT1 or CMT4. CMTX5 is also known as Rosenberg-Chutorian syndrome. Some researchers believe that this condition is not actually a form of Charcot-Marie-Tooth disease. Instead, they classify it as a separate disorder characterized by peripheral nerve problems, deafness, and vision loss.
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