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ICD-10/G60.0

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

Billing Status: YES. This is a valid, specific, and billable ICD-10-CM reference.

Inpatient Payment Groups (MS-DRG)

MS-DRGs this diagnosis helps define, as principal or secondary, per the CMS ICD-10-CM/PCS MS-DRG Definitions Manual v43.0 (FY2026), Appendix B.

  • MS-DRG 073 — CRANIAL AND PERIPHERAL NERVE DISORDERS WITH MCC (MDC 01)
  • MS-DRG 074 — CRANIAL AND PERIPHERAL NERVE DISORDERS WITHOUT MCC (MDC 01)

A diagnosis appearing in a group's logic does not by itself determine the DRG assigned to a stay; the grouper uses the full claim.

Code Set: Valid FY2026 and FY2027. FY2026 took effect October 1, 2025.

Official Registry Overview & Definition

Hereditary motor and sensory neuropathy is a billable ICD-10-CM diagnosis code (G60.0).

Official Tabular Instructional Notes

Sequencing, inclusion, and exclusion notes published for G60.0 in the official ICD-10-CM tabular list.

Inclusion Terms

Alternative terms the tabular list files under this code.

  • 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

Conditions that can never be reported with this code; the two are mutually exclusive.

  • neuralgia NOS (M79.2)
  • neuritis NOS (M79.2)
  • peripheral neuritis in pregnancy (O26.82-)
  • radiculitis NOS (M54.10)

Nearest Codes in This Family

Official ICD-10-CM classifications closest to G60.0 in its code family, with their registry titles.

  • G60 — Hereditary and idiopathic neuropathy
  • G60.1 — Refsum's disease
  • G60.2 — Neuropathy in association with hereditary ataxia
  • G60.3 — Idiopathic progressive neuropathy
  • G60.8 — Other hereditary and idiopathic neuropathies
  • G60.9 — Hereditary and idiopathic neuropathy, unspecified

View all codes in the G60 family

Indexed Clinical Terms (23)

Clinical term phrases from the official ICD-10-CM Index to Diseases and Injuries that map to this code.

  • 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-Marietype (-Tooth)
  • 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