- G60.0 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
- The 2024 edition of ICD-10-CM G60.0 became effective on October 1, 2022.
- This is the American ICD-10-CM version of G60.0 – other international versions of ICD-10 G60.0 may differ.
ICD-10-CM G60.0 is grouped within Diagnostic Related Group(s):
- 073 Cranial and peripheral nerve disorders with mcc
- 074 Cranial and peripheral nerve disorders without mcc
Applicable To
- 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
Code History
- 2016 (effective 10/1/2015): New code (first year of non-draft ICD-10-CM)
- 2016 (effective 10/1/2015): No change
- 2017 (effective 10/1/2016): No change
- 2018 (effective 10/1/2017): No change
- 2019 (effective 10/1/2018): No change
- 2020 (effective 10/1/2019): No change
- 2021 (effective 10/1/2020): No change
- 2022 (effective 10/1/2021): No change
- 2024 (effective 10/1/2022): No change
Diagnosis Index entries containing back-references to G60.0:
- Roussy-Lévy > Ataxia, ataxy, ataxic R27.0
- Charcot-Marie-Tooth > Atrophy, atrophic (of)
- neuropathic (peroneal) (progressive) > muscle, muscular (diffuse) (general) (idiopathic) (primary) M62.50
- peroneal > muscle, muscular (diffuse) (general) (idiopathic) (primary) M62.50
- due to or associated with > spine (acquired) (angular) (idiopathic) (incorrect) (postural) Q67.5
- Charcot-Marie-Tooth disease > due to or associated with G60.0
- Charcot-Marie type (-Tooth) > progressive (hereditary) G71.09
- Déjérine-Sottas > Neuritis (rheumatoid) M79.2
- interstitial hypertrophic progressive > Neuritis (rheumatoid) M79.2
- progressive hypertrophic interstitial > Neuritis (rheumatoid) M79.2
- Déjérine-Sottas > Neuropathy, neuropathic G62.9
- motor and sensory (types I-IV) > hereditary G60.9
- hypertrophic > Neuropathy, neuropathic G62.9
- Charcot-Marie-Tooth > hypertrophic G60.0
- Déjérine-Sottas > hypertrophic G60.0
- interstitial progressive > hypertrophic G60.0
- of infancy > hypertrophic G60.0
- motor and sensory > Neuropathy, neuropathic G62.9
- hereditary (types I-IV) > motor and sensory G60.0
- progressive > Neuropathy, neuropathic G62.9
- hypertrophic interstitial > progressive G60.0
- Charcot-Marie-Tooth type > Paralysis, paralytic (complete) (incomplete) G83.9