2027 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 2027 ICD-10-CM dataset · Effective Oct 1, 2026 – Sep 30, 2027

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 2027 (October 1, 2026 through September 30, 2027) and groups to MS-DRG 73 through 74. In AHRQ's Clinical Classifications Software (CCSR), this diagnosis falls under Polyneuropathies.

G60.0 does not risk-adjust for Medicare Advantage under the CMS-HCC V28 model. It still risk-adjusts in the ESRD (V21) category 75 for payment year 2027.

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

Medicare Risk Adjustment (HCC)Billing

G60.0 does not risk-adjust for Medicare Advantage under the CMS-HCC V28 model, but it maps to payment categories in the other CMS models shown below.

CMS-HCC V28 (Medicare Advantage Payment Model)
Not mapped
no payment category in the model that pays 100% of MA risk scores
Prior Model (CMS-HCC V24)
Not mapped under V24
this diagnosis newly risk-adjusts under the V28 model
Other CMS Models
ESRD (V21): HCC 75
ESRD V21 weights: 0.059 dialysis, 0.284–0.323 functioning graft
Part D (RxHCC)
Not mapped
G60.0 does not risk-adjust in the RxHCC prescription drug model

Source: CMS Payment Year 2027 risk adjustment mappings and model software. Weights are relative factors, not dollar amounts; a beneficiary's total RAF also includes demographics and interactions. Browse all CMS-HCC categories.

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
  • 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
  • Chronic axonal neuropathy
  • Coenzyme Q10 deficiency
  • Congenital axonal neuropathy with encephalopathy
  • Congenital polyneuropathy
  • COQ7 gene related distal hereditary motor neuropathy
  • 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
  • Lipodystrophy, demyelinating peripheral sensory motor neuropathy 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
  • Neonatal muscle tone disorder
  • 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
  • Segmental demyelination of peripheral nerve
  • 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

Instructional NotesGuidance

Instructions from the official ICD-10-CM Tabular List that apply to G60.0: its own notes plus those printed at block G60-G65 and Chapter 6. A note printed at a category, block or chapter applies to every code under it.

Applicable To

Conditions this code is used for: synonyms of the title or, for "other specified" codes, the conditions assigned to it. The list is not exhaustive.

  • 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

Excludes1

Not coded here: the excluded code is never reported together with this one, unless the two conditions are unrelated.

From Block G60-G65 Polyneuropathies and other disorders of the peripheral nervous system applies to 24 codes

Excludes2

Not included here: the excluded condition is not part of this code, but a patient may have both, so both codes may be reported.

From Chapter 6 (G00-G99) Diseases of the nervous system applies to 700 codes
  • certain conditions originating in the perinatal period (P04-P96)
  • certain infectious and parasitic diseases (A00-B99)
  • complications of pregnancy, childbirth and the puerperium (O00-O9A)
  • congenital malformations, deformations, and chromosomal abnormalities (Q00-Q99)
  • endocrine, nutritional and metabolic diseases (E00-E88)
  • injury, poisoning and certain other consequences of external causes (S00-T88)
  • neoplasms (C00-D49)
  • symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)

Source: CMS ICD-10-CM Tabular List. How to read instructional notes.

Referenced in Other NotesGuidance

Instructional notes printed at other codes that name G60.0, its category, or a range that includes it.

Excludes2 1

These codes carry an Excludes2 note naming G60.0: its condition is not part of those codes, and both may be reported when the patient has both.

  • G11 Hereditary ataxia
    hereditary and idiopathic neuropathy (G60.-) names G60.-, which includes this code

Code First 1

These codes say to code first a condition named in the note, and G60.0 is one of the conditions named.

  • M49 Spondylopathies in diseases classified elsewhere
    Charcot-Marie-Tooth disease (G60.0)

Index to Diseases and InjuriesGuidance

Alphabetical index entries that point to this code.

Clinical ClassificationClinical

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

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

Clinical InformationClinical

  • Hereditary Sensory and Motor Neuropathy

    a group of slowly progressive inherited disorders affecting motor and sensory peripheral nerves. subtypes include hmsns i-vii. hmsn i and ii both refer to charcot-marie-tooth disease. hmsn iii refers to hypertrophic neuropathy of infancy. hmsn iv refers to refsum disease. hmsn v refers to a condition marked by a hereditary motor and sensory neuropathy associated with spastic paraplegia (see spastic paraplegia, hereditary). hmsn vi refers to hmsn associated with an inherited optic atrophy (optic atrophies, hereditary), and hmsn vii refers to hmsn associated with retinitis pigmentosa. (from adams et al., principles of neurology, 6th ed, p1343)

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 2017–2026No changes
FY 2027CurrentCurrent code set, no changesEffective October 1, 2026 through September 30, 2027.

Questions About G60.0Overview

What is the ICD-10 code for hereditary motor and sensory neuropathy?

The ICD-10-CM code for hereditary motor and sensory neuropathy is G60.0 (sometimes written as G600). It is billable on HIPAA-covered claims from October 1, 2026 through September 30, 2027.

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, 2026 through September 30, 2027.

What MS-DRG does G60.0 group to?

When hereditary motor and sensory neuropathy is the principal diagnosis on an inpatient stay, it groups to MS-DRG 74, 73, with relative weights from 1.0172 to 1.5773 depending on complications. Higher weights mean higher Medicare reimbursement.

Can G60.0 be reported with M79.2?

Not as a rule. The Excludes1 note at block G60-G65, which applies to G60.0, lists "neuralgia NOS (M79.2)". An Excludes1 note means the excluded code is never reported together with this one; the only exception is when the two conditions are unrelated to each other (Official Guidelines, Section I.A.12.a).

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.

Does G60.0 risk-adjust for Medicare Advantage payment?

Not for Medicare Advantage: G60.0 maps to no category in the CMS-HCC V28 model. It still risk-adjusts in the ESRD (V21) category 75 (Polyneuropathy).