2026 ICD-10-CM Diagnosis Code G60.0Hereditary motor and sensory neuropathy

ICD-10-CM Codes›G00–G99›G60-G65›G60

ICD-10-CM G60.0
CMSSource: CMS FY 2026 ICD-10-CM dataset · Effective Oct 1, 2025 – Sep 30, 2026

G60.0 is a billable ICD-10-CM diagnosis code for hereditary motor and sensory neuropathy. It is valid on HIPAA claims for fiscal year 2026 (October 1, 2025 through September 30, 2026). In AHRQ's Clinical Classifications Software (CCSR), this diagnosis falls under Polyneuropathies.

Code Identity

ICD-10-CM Code
G60.0
Billable Status
Yes — Valid for Submission
Code Describes
Hereditary motor and sensory neuropathy
Short Description
Hereditary motor and sensory neuropathy
Same as the full description in the CMS dataset.
Parent Code
G60
Hereditary and idiopathic neuropathy

Code Classification

ChapterG00–G99Diseases of the nervous system
SectionG60-G65Polyneuropathies and other disorders of the peripheral nervous system
CategoryG60Hereditary and idiopathic neuropathy
This CodeG60.0Hereditary motor and sensory neuropathy

Approximate SynonymsGuidance

Alternate terms and clinical phrases that map to this code.

  • 46,XY gonadal dysgenesis, motor and sensory neuropathy syndrome
  • Acute hepatic failure
  • Acute infantile liver failure, cerebellar ataxia, peripheral sensory motor neuropathy syndrome
  • Atrophy of muscle of lower leg
  • Atrophy of peroneal muscle
  • Autosomal dominant Charcot-Marie-Tooth disease type 2
  • Autosomal dominant Charcot-Marie-Tooth disease type 2 due to DGAT2 mutation
  • Autosomal dominant Charcot-Marie-Tooth disease type 2 due to KIF5A mutation
  • Autosomal dominant Charcot-Marie-Tooth disease type 2 due to TFG mutation
  • Autosomal dominant Charcot-Marie-Tooth disease type 2 with giant axons
  • Autosomal dominant Charcot-Marie-Tooth disease type 2A1
  • Autosomal dominant Charcot-Marie-Tooth disease type 2A2
  • Autosomal dominant Charcot-Marie-Tooth disease type 2B
  • Autosomal dominant Charcot-Marie-Tooth disease type 2C
  • Autosomal dominant Charcot-Marie-Tooth disease type 2D
  • Autosomal dominant Charcot-Marie-Tooth disease type 2DD
  • Autosomal dominant Charcot-Marie-Tooth disease type 2E
  • Autosomal dominant Charcot-Marie-Tooth disease type 2F
  • Autosomal dominant Charcot-Marie-Tooth disease type 2I
  • Autosomal dominant Charcot-Marie-Tooth disease type 2J
  • Autosomal dominant Charcot-Marie-Tooth disease type 2K
  • Autosomal dominant Charcot-Marie-Tooth disease type 2L
  • Autosomal dominant Charcot-Marie-Tooth disease type 2M
  • Autosomal dominant Charcot-Marie-Tooth disease type 2N
  • Autosomal dominant Charcot-Marie-Tooth disease type 2O
  • Autosomal dominant Charcot-Marie-Tooth disease type 2Q
  • Autosomal dominant Charcot-Marie-Tooth disease type 2U
  • Autosomal dominant Charcot-Marie-Tooth disease type 2V
  • Autosomal dominant Charcot-Marie-Tooth disease type 2W
  • Autosomal dominant Charcot-Marie-Tooth disease type 2Y
  • Autosomal dominant Charcot-Marie-Tooth disease type 2Z
  • Autosomal dominant distal axonal motor neuropathy, myofibrillar myopathy syndrome
  • Autosomal dominant distal hereditary motor neuropathy
  • Autosomal dominant intermediate Charcot-Marie-Tooth disease type A
  • Autosomal dominant intermediate Charcot-Marie-Tooth disease type B
  • Autosomal dominant intermediate Charcot-Marie-Tooth disease type C
  • Autosomal dominant intermediate Charcot-Marie-Tooth disease type D
  • Autosomal dominant intermediate Charcot-Marie-Tooth disease type E
  • Autosomal dominant intermediate Charcot-Marie-Tooth disease type F
  • Autosomal dominant intermediate Charcot-Marie-Tooth disease with neuropathic pain
  • Autosomal dominant slowed nerve conduction velocity
  • Autosomal recessive axonal Charcot-Marie-Tooth disease due to copper metabolism defect
  • Autosomal recessive Charcot-Marie-Tooth disease type 2
  • Autosomal recessive Charcot-Marie-Tooth disease type 2X
  • Autosomal recessive Charcot-Marie-Tooth disease with hoarseness
  • Autosomal recessive distal hereditary motor neuropathy
  • Autosomal recessive intermediate Charcot-Marie-Tooth disease type A
  • Autosomal recessive intermediate Charcot-Marie-Tooth disease type B
  • Autosomal recessive intermediate Charcot-Marie-Tooth disease type C
  • Autosomal recessive intermediate Charcot-Marie-Tooth disease type D
  • Autosomal recessive lethal neonatal axonal sensorimotor polyneuropathy
  • Axonal neuropathy
  • Charcot-Marie-Tooth disease type 2B1
  • Charcot-Marie-Tooth disease type 2B2
  • Charcot-Marie-Tooth disease type 2B5
  • Charcot-Marie-Tooth disease type 2H
  • Charcot-Marie-Tooth disease type 2P
  • Charcot-Marie-Tooth disease type 2R
  • Charcot-Marie-Tooth disease type 2S
  • Charcot-Marie-Tooth disease type 2T
  • Charcot-Marie-Tooth disease type 4
  • Charcot-Marie-Tooth disease type 4A
  • Charcot-Marie-Tooth disease type 4B1
  • Charcot-Marie-Tooth disease type 4B2
  • Charcot-Marie-Tooth disease type 4B3
  • Charcot-Marie-Tooth disease type 4C
  • Charcot-Marie-Tooth disease type 4D
  • Charcot-Marie-Tooth disease type 4E
  • Charcot-Marie-Tooth disease type 4F
  • Charcot-Marie-Tooth disease type 4G
  • Charcot-Marie-Tooth disease type 4H
  • Charcot-Marie-Tooth disease type 4J
  • Charcot-Marie-Tooth disease type ID
  • Charcot-Marie-Tooth disease type IE
  • Charcot-Marie-Tooth disease type IF
  • Charcot-Marie-Tooth disease, deafness, intellectual disability syndrome
  • Charcot-Marie-Tooth disease, type IA
  • Charcot-Marie-Tooth disease, type IB
  • Charcot-Marie-Tooth disease, type IC
  • Charcot-Marie-Tooth disease, type II
  • Charcot-Marie-Tooth Neuropathy Type 4
  • Congenital axonal neuropathy with encephalopathy
  • Congenital polyneuropathy
  • Déjérine-Sottas disease
  • Disorder of copper metabolism
  • Distal hereditary motor neuropathy type 5
  • Distal hereditary motor neuropathy type 7
  • Distal spinal muscular atrophy
  • DNAJB2-related Charcot-Marie-Tooth disease type 2
  • Hereditary hypertrophic neuropathy with paraproteinemia
  • Hereditary liability to pressure palsies
  • Hereditary motor and sensory neuropathy
  • Hereditary motor and sensory neuropathy Okinawa type
  • Hereditary motor and sensory neuropathy with acrodystrophy
  • Hereditary motor and sensory neuropathy with optic atrophy
  • Hereditary motor and sensory neuropathy with retinitis pigmentosa
  • Hereditary sensorimotor neuropathy with hyperelastic skin
  • Hereditary sensory and autonomic neuropathy type 1B
  • Hereditary sensory and autonomic neuropathy type I
  • Hereditary sensory and autonomic neuropathy type II
  • Hereditary sensory and autonomic neuropathy with deafness and global delay
  • Hereditary sensory autonomic neuropathy type IA
  • Hereditary sensory autonomic neuropathy type IC
  • Hereditary sensory autonomic neuropathy type ID
  • Hereditary sensory autonomic neuropathy type IE
  • Hereditary sensory autonomic neuropathy type IIA
  • Hereditary sensory autonomic neuropathy type IIB
  • Hereditary sensory-motor neuropathy, type I
  • Hereditary thermosensitive neuropathy
  • Hypertrophic interstitial neuropathy
  • Infantile-onset axonal motor and sensory neuropathy, optic atrophy, neurodegenerative syndrome
  • Microcephalus, complex motor and sensory axonal neuropathy syndrome
  • Mixed sensory-motor polyneuropathy
  • MME-related autosomal dominant Charcot Marie Tooth disease type 2
  • Motor polyneuropathy
  • Palmoplantar keratoderma, hereditary motor and sensory neuropathy syndrome
  • Paralysis of glottis
  • Peripheral axonal neuropathy
  • PMP2-related Charcot-Marie-Tooth disease type 1
  • Roussy-Lévy syndrome
  • Sensory polyneuropathy
  • Severe early-onset axonal neuropathy due to mitofusin 2 deficiency
  • SURF1-related Charcot-Marie-Tooth disease type 4
  • Vocal cord paralysis
  • X-linked Charcot-Marie-Tooth disease type 1
  • X-linked Charcot-Marie-Tooth disease type 2
  • X-linked Charcot-Marie-Tooth disease type 3
  • X-linked Charcot-Marie-Tooth disease type 4
  • X-linked Charcot-Marie-Tooth disease type 5
  • X-linked Charcot-Marie-Tooth disease type 6
  • X-linked distal hereditary motor neuropathy
  • X-linked hereditary motor and sensory neuropathy
  • Young adult-onset distal hereditary motor neuropathy

Tabular List NotesGuidance

Coding notes and annotation back-references applicable to this code.

Inclusion Terms

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

Index to Diseases and InjuriesGuidance

Alphabetical index entries that point to this code.

External Cause of Injuries IndexGuidance

References for this code in the External Cause of Injuries Index.

    • Ataxia, ataxy, ataxic
      • Roussy-Lévy
    • Atrophy, atrophic(of)
      • Charcot-Marie-Tooth
    • Atrophy, atrophic(of)
      • muscle, muscular (diffuse) (general) (idiopathic) (primary)
        • neuropathic (peroneal) (progressive)
    • Atrophy, atrophic(of)
      • muscle, muscular (diffuse) (general) (idiopathic) (primary)
        • peroneal
    • Charcot-Marie-Tooth disease, paralysis or syndrome
    • Curvature
      • spine (acquired) (angular) (idiopathic) (incorrect) (postural)
        • due to or associated with
          • Charcot-Marie-Tooth disease
    • Déjérine-Sottas disease or neuropathy(hypertrophic)
    • Dystrophy, dystrophia
      • muscular
        • progressive (hereditary)
          • Charcot-Marie (-Tooth) type
    • Marie-Charcot-Tooth neuropathic muscular atrophy
    • Neuritis(rheumatoid)
      • Déjérine-Sottas
    • Neuritis(rheumatoid)
      • interstitial hypertrophic progressive
    • Neuritis(rheumatoid)
      • progressive hypertrophic interstitial
    • Neuropathy, neuropathic
      • Déjérine-Sottas
    • Neuropathy, neuropathic
      • hereditary
        • motor and sensory (types I-IV)
    • Neuropathy, neuropathic
      • hypertrophic
    • Neuropathy, neuropathic
      • hypertrophic
        • Charcot-Marie-Tooth
    • Neuropathy, neuropathic
      • hypertrophic
        • Déjérine-Sottas
    • Neuropathy, neuropathic
      • hypertrophic
        • interstitial progressive
    • Neuropathy, neuropathic
      • hypertrophic
        • of infancy
    • Neuropathy, neuropathic
      • motor and sensory
        • hereditary (types I-IV)
    • Neuropathy, neuropathic
      • progressive
        • hypertrophic interstitial
    • Paralysis, paralytic(complete) (incomplete)
      • Charcot-Marie-Tooth type
    • Roussy-Lévy syndrome

Clinical ClassificationClinical

AHRQ’s CCSR groups this code into broader clinical categories.

CCSR NVS015
Polyneuropathies
Default principal diagnosis: inpatient Yes · outpatient Yes

Clinical InformationClinical

  • Vocal Cord Paralysis

    congenital or acquired paralysis of one or both vocal cords. this condition is caused by defects in the central nervous system, the vagus nerve and branches of laryngeal nerves. common symptoms are voice disorders including hoarseness or aphonia.

  • Acute Motor and Sensory Axonal Neuropathy|Acute Motor And Sensory Axonal Neuropathy|Acute Motor-Sensory Axonal Neuropathy|Acute Motor-Sensory Axonal Neuropathy

    a subtype of guillain-barre syndrome that targets sensory motor axons, and is characterized by acute onset of quadriparesis, distal sensory loss, areflexia, and respiratory insufficiency.

  • Acute Motor Axonal Neuropathy|AMAN

    a subtype of guillain-barre syndrome that targets motor axons, and is characterized by symmetric limb weakness, diffuse areflexia, facial and oropharyngeal muscle weakness, and respiratory insufficiency.

  • Axonal Neuropathy

    any nerve disorder affecting the axon of a nerve.

  • GAN wt Allele|GAN1|Giant Axonal Neuropathy (Gigaxonin) Gene|Gigaxonin wt Allele|KLHL16

    human gan wild-type allele is located in the vicinity of 16q24.1 and is approximately 65 kb in length. this allele, which encodes gigaxonin protein, is involved in both ubiquitination and neurofilament structure. mutation of the gene is associated with giant axonal neuropathy.

  • Giant Axonal Neuropathy

    a rare inherited disorder affecting the neurofilaments. it is caused by mutations in the gan gene. it is characterized by the presence of abnormally large nerve cell axons. signs and symptoms include difficulty walking, sensory disturbances, lack of motor coordination and abnormal reflexes in the limbs.

  • Spinocerebellar Ataxia, Autosomal Recessive, with Axonal Neuropathy 2|AOA2|Ataxia with Oculomotor Apraxia Type 2|SCAN2

    an autosomal recessive condition caused by mutation(s) in the setx gene, encoding probable helicase senataxin. it is characterized by juvenile onset progressive cerebellar ataxia, axonal sensorimotor peripheral neuropathy, and increased concentrations of serum alpha-fetoprotein. oculomotor apraxia is common, but is not always present.

Patient EducationClinical

Charcot-Marie-Tooth Disease

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.

Read the full article at MedlinePlus

Courtesy of MedlinePlus, a service of the U.S. National Library of Medicine.

Convert G60.0 to ICD-9-CMHistory

The closest ICD-9-CM equivalents under the General Equivalence Mappings.

ICD-9-CM
356.0 Hered periph neuropathy
Approximate The match is approximate rather than exact.
ICD-9-CM
356.1 Peroneal muscle atrophy
Approximate The match is approximate rather than exact.
ICD-9-CM
356.2 Hered sensory neuropathy
Approximate The match is approximate rather than exact.

Code HistoryHistory

FY 2016AddedAdded to the ICD-10-CM code setEffective October 1, 2015, the first year of ICD-10-CM.
FY 2017–2025No changes
FY 2026CurrentCurrent code set, no changesEffective October 1, 2025 through September 30, 2026.

Questions About G60.0Overview

Is G60.0 (Hereditary and idiopathic neuropathy) a billable code?

Yes. This is a billable ICD-10-CM code, specific enough to report hereditary motor and sensory neuropathy on HIPAA-covered claims from October 1, 2025 through September 30, 2026.

What is the ICD-9 equivalent of G60.0?

Under the General Equivalence Mappings, hereditary motor and sensory neuropathy converts to ICD-9-CM 356.0 (hered periph neuropathy), 356.1 (peroneal muscle atrophy), and 356.2 (hered sensory neuropathy). The mapping is approximate, so confirm the match fits the documentation.

Footnotes

[1] Chronic - a chronic condition code indicates a condition lasting 12 months or longer and its effect on the patient based on one or both of the following criteria:

  • The condition results in the need for ongoing intervention with medical products,treatment, services, and special equipment
  • The condition places limitations on self-care, independent living, and social interactions.