G60.8 is the ICD-10 code for Other hereditary and idiopathic neuropathies. 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 G60.8 includes
Conditions and terms that are coded here.
- Morvan disease
- Nelaton syndrome
- Sensory neuropathy:
- dominantly inherited
- recessively inherited
G60.8 in national editions
Countries report with their own edition of ICD-10. Most keep the WHO code and add more specific codes beneath it.
G60.8Andra specificerade hereditära och idiopatiska neuropatier
G60.8Annen spesifisert arvelig eller idiopatisk nevropati
DG608Anden form for arvelig motorisk-sensorisk neuropati
- DG608AMorvans sygdom
- DG608BNelatons syndrom
- DG608CRecessiv arvelig sensorisk neuropati
- DG608DDominant arvelig sensorisk neuropati
G60.8Muu perinnöllinen idiopaattinen ääreishermosairaus
G60.8Sonstige hereditäre und idiopathische Neuropathien
G60.8Autres neuropathies héréditaires et idiopathiques
G60.8overige gespecificeerde hereditaire- en idiopathische neuropathieën
G60.8Other hereditary and idiopathic neuropathies
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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