G60.0 is the ICD-10 code for Hereditary motor and sensory neuropathy. It is a four-character subcategory of G60 (Hereditary and idiopathic neuropathy), the most specific level in the WHO edition. It belongs to the block G60–G64 (Polyneuropathies and other disorders of the peripheral nervous system) in Chapter VI, Diseases of the nervous system.
- Code type
- Subcategory (4 characters)
- Chapter
- VI · G00–G99
- Classification
- WHO ICD-10, 2019 version
What G60.0 includes
Conditions and terms that are coded here.
- Disease:
- Charcot-Marie-Tooth
- Déjerine-Sottas
- Hereditary motor and sensory neuropathy, types I-IV
- Hypertrophic neuropathy of infancy
- Peroneal muscular atrophy (axonal type)(hypertrophic type)
- Roussy-Lévy syndrome
G60.0 in national editions
Countries report with their own edition of ICD-10. Most keep the WHO code and add more specific codes beneath it.
G60.0Arvelig motorisk eller sensorisk nevropati
DG600Arvelig motorisk-sensorisk neuropati
- DG600AHypertrofisk peroneal muskelatrofi
- DG600BNeuropatisk muskelatrofi
- DG600CAxonal peroneal muskelatrofi
- DG600DAtrophia Charcot-Marie-Tooth
- DG600EDéjerine-Sottas sygdom
- DG600FHypertrofisk neuropati i barndommen
- DG600GArvelig motorisk-sensorisk neuropati, type I-IV
- DG600IRoussy-Lévys syndrom
G60.0Perinnöllinen motorinen ja sensorinen ääreishermosairaus
G60.0Hereditäre sensomotorische Neuropathie
G60.0Neuropathie héréditaire motrice et sensorielle
G60.0hereditaire motorische- en sensorische-neuropathie
G60.0Hereditary motor and sensory neuropathy
Based on the World Health Organization’s International Statistical Classification of Diseases and Related Health Problems, 10th revision (ICD-10), 2019 version, and the national editions published by each country’s health authority. This page is a reference, not coding advice; follow your national coding rules when you report.
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