G60.0
Hereditary motor and sensory neuropathy
G60.0 (also written G600) is a billable ICD-10-CM diagnosis code for hereditary motor and sensory neuropathy. It is part of the FY2027 code set, effective October 1, 2026. It is one of the 6 codes in category G60 (Hereditary and idiopathic neuropathy). The Alphabetic Index lists it under 23 entries. Its coding notes include 4 Excludes1 entries and 8 Excludes2 entries.
Excludes1
Not coded here. The listed conditions generally should not be reported together.
Excludes2
Not included here. Both codes may be reported if the patient has both conditions.
Also from chapter/block level (8 notes)
- 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)
Care settings
How CMS programs treat this code. These are CMS claim edits and list entries, not coverage or eligibility rules.
Home Health Primary
Accepted as the primary (principal) diagnosis on a home health claim. The Home Health Grouper assigns it to the Neuro Rehabilitation clinical group.
Source: CMS Home Health Grouper Software v07.2.26, effective October 1, 2026IRF 60% Rule
On the CMS list of diagnoses used to determine presumptive compliance with the IRF 60 percent rule.
Source: CMS IRF Presumptive Compliance-3, FY 2027 IRF PPS final rule files, effective for discharges on or after October 1, 2026Inclusion terms
Conditions classified to 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
Alphabetic Index terms
Terms the official Alphabetic Index lists for this code. 23 entries
- 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
- Dystrophy, dystrophia, muscular, progressive (hereditary), Charcot-Marie (-Tooth) type
- Déjérine-Sottas disease or neuropathy (hypertrophic)
- Marie-Charcot-Tooth neuropathic muscular atrophy
- Neuritis (rheumatoid), Déjérine-Sottas
- Neuritis (rheumatoid), interstitial hypertrophic progressive
- Neuritis (rheumatoid), progressive hypertrophic interstitial
Show 11 more
- 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