" /> Motor neuron disease - CISMeF





ICD-11 code : 8B60;

Preferred Label : Motor neuron disease;

ICD-11 definition : Motor neuron disease is a neurodegenerative disorder of undetermined etiology, characterized by degeneration of upper motor neurons (cortical Betz cells and corticospinal tract) or lower motor neurons (ventral horns of spinal cord and cranial nerve motor nuclei) or both. Features of involvement of lower motor neurons (LMN) are atrophy, weakness, fasciculations, hypotonia, decreased or absent deep tendon reflexes. Features of involvement of upper motor neurons (UMN) are spasticity, exaggerated deep tendon reflexes, and extensor plantar responses. Depending on the site of onset and the presence of UMN or LMN features or both, MND has varying patterns and distributions of signs and symptoms.;

ICD-11 synonym : motor neurone disease; MND - [motor neurone disease];

ICD-11 acronym : MND;

ICD-11 inclusion : lateral paralysis; spinal progressive amyotrophy; creeping paralysis; Lou Gehrig disease; bulbar motor neuron disease; progressive spinal cord paralysis; lateral incomplete paralysis; bulbar paralysis; polioencephalitis; inferior; wasting paralysis; progressive paralysis; lateral complete paralysis; creeping palsy; hereditary motor neuron disease; progressive atrophic paralysis; lateral spine sclerosis; Duchenne-Aran atrophy; anterior horn cell disorder; wasting palsy; Duchenne-Aran muscle atrophy; bulbar palsy; progressive spinal paralysis; bulbar syndrome; chronic bulbar palsy; inferior poliencephalitis; supranuclear bulbar paralysis; anterior horn cell disease; lateral spinal sclerosis; chronic bulbar paralysis; cruveilhier; labioglossal paralysis;

ICD-11 "other" category code : 8B60.Y;

ICD-11 "unspecified" category code : 8B60.Z;

Details


You can consult :

Motor neuron disease is a neurodegenerative disorder of undetermined etiology, characterized by degeneration of upper motor neurons (cortical Betz cells and corticospinal tract) or lower motor neurons (ventral horns of spinal cord and cranial nerve motor nuclei) or both. Features of involvement of lower motor neurons (LMN) are atrophy, weakness, fasciculations, hypotonia, decreased or absent deep tendon reflexes. Features of involvement of upper motor neurons (UMN) are spasticity, exaggerated deep tendon reflexes, and extensor plantar responses. Depending on the site of onset and the presence of UMN or LMN features or both, MND has varying patterns and distributions of signs and symptoms.

Nous contacter.
09/05/2025


[Home] [Top]

© Rouen University Hospital. Any partial or total use of this material must mention the source.