ICD 10 Codes >> Diseases of the nervous system (G00-G99) G00-G99 >>Polyneuropathies and other disorders of the peripheral nervous system (G60-G65) G60-G65 >> Hereditary and idiopathic neuropathy G60.-

ICD 10 Code G60.0

Hereditary motor and sensory neuropathy

2017 Billable/Specific Code

Autosomal dominant Charcot-Marie-Tooth disease type 2F (CMT2F) is a form of axonal Charcot-Marie-Tooth disease, a peripheral sensorimotor neuropathy. CMT2F is characterized by symmetric weakness primarily occurring in the lower limbs (distal muscles in a majority of cases) and reaching the arms only after 5 to 10 years, occasional and predominantly distal sensory loss and reduced tendon reflexes. CMT2F presents with gait anomaly between the 1st and 6th decade and early onset is generally associated to a more severe phenotype which may include foot drop.
  • G60.0 is a billable ICD-10 medical codes that provide a detailed representation of a patient's conditions or diagnoses.
  • ICD-10-CM codes are used for a variety of purposes, including statistics and for billing and claims reimbursement.
  • This is the American ICD 10 CM Version Of G60.0 allows for the capture of data regarding signs, symptoms, risk factors and comorbidities to better describe the clinical issue overall.

    Inclusion Term For Icd 10 Code G60.0

    • Charcot-Marie-Tooth disease
    • Déjérine-Sottas disease
    • Hereditary motor and sensory neuropathy, types I-IV
    • Hypertrophic neuropathy of infancy
    • Peroneal muscular atrophy (axonaltype) (hypertrophictype)
    • Roussy-Levy syndrome

Reverse Index Lookup for ICD 10 CM CODE G60.0


The following ICD-10-CM Index entries contain back-references to ICD-10-CM G60.0:
  • Ataxia, ataxy, ataxic   R27.0
    • Roussy-Lévy   G60.0
    • Charcot-Marie-Tooth   G60.0
    • muscle, muscular   M62.50
      • neuropathic   G60.0
      • peroneal   G60.0
  • Charcot-Marie-Tooth disease, paralysis or syndrome   G60.0
      • due to or associated with
        • Charcot-Marie-Tooth disease seeAlso : subcategory M49.8  G60.0
  • Déjérine-Sottas disease or neuropathy   G60.0
    • muscular   G71.0
      • progressive   G71.0
        • Charcot-Marie   G60.0
  • Marie-Charcot-Tooth neuropathic muscular atrophy   G60.0
  • Neuritis   M79.2
    • Déjérine-Sottas   G60.0
    • interstitial hypertrophic progressive   G60.0
    • progressive hypertrophic interstitial   G60.0
  • Neuropathy, neuropathic   G62.9
    • Déjérine-Sottas   G60.0
    • hereditary   G60.9
      • motor and sensory   G60.0
    • hypertrophic   G60.0
      • Charcot-Marie-Tooth   G60.0
      • Déjérine-Sottas   G60.0
      • interstitial progressive   G60.0
      • of infancy   G60.0
    • motor and sensory SeeAlso: Polyneuropathy
      • hereditary   G60.0
    • progressive
      • hypertrophic interstitial   G60.0
  • Paralysis, paralytic   G83.9
    • Charcot-Marie-Tooth type   G60.0
  • Roussy-Lévy syndrome   G60.0

  • SNOMed Terms:
    • Acrodystrophic neuropathy
    • Agenesis of corpus callosum with peripheral neuropathy
    • Agenesis of corpus callosum with peripheral neuropathy (disorder)
    • Agenesis of corpus callosum with polyneuropathy
    • Andermann syndrome
    • Autosomal dominant Charcot-Marie-Tooth disease type 2A1
    • Autosomal dominant Charcot-Marie-Tooth disease type 2A1 (disorder)
    • Autosomal dominant Charcot-Marie-Tooth disease type 2B
    • Autosomal dominant Charcot-Marie-Tooth disease type 2B (disorder)
    • Autosomal dominant Charcot-Marie-Tooth disease type 2C

    • Major Diagnostic Categories
      M.D.C

      • MDC Category : 01
      • MDC Type : Medical
      • Description : Diseases and Disorders of the Nervous System

    • Medicare Severity-Diagnosis Related Groups
      MS-DRG

      • DRG Range: 073-074
        • 073 -- CRANIAL & PERIPHERAL NERVE DISORDERS W MCC
        • 074 -- CRANIAL & PERIPHERAL NERVE DISORDERS W/O MCC

    • Clinical Classifications Software
      CCS

      • CCS Category Number : 95
      • Description : Other nervous system disorders
      • Multi CCS Level 1 Number : 6
      • Level 1 Description : Diseases of the nervous system and sense organs
      • Multi CCS Level 2 Number : 6.9
      • Level 2 Description : Other nervous system disorders [95.]

    • Prevention Quality Indicators (admissions for 'ambulatory care sensitive conditions')
      ACSC

      G60.0 ICD CODE is not Assigned For ACSA Admit

    • New York University Emergency Department visit severity algorithm
      NYU ED

      Non-emergent - 0%
      Emergent/Primary Care Treatable - 0%
      Emergent - ED Care Needed - Preventable/Avoidable - 0%
      Emergent - ED Care Needed - Not Preventable/Avoidable - 0%
      Primary diagnosis of injury 0%
      Primary diagnosis of mental health problems 0%
      Primary diagnosis of substance abuse 0%
      Primary diagnosis of Alcohol 0%
      Unclassified 100%

    Also called: Hereditary motor and sensory neuropathy, Peroneal muscular atrophyCharcot-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 ...

    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 (...

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