Amyotrophic lateral sclerosis

Disease Export to PDF
Name:
Amyotrophic lateral sclerosis
Description:
A neurodegenerative disease characterized by progressive muscular paralysis reflecting degeneration of motor neurons in the primary motor cortex, corticospinal tracts, brainstem and spinal cord.
ORPHAcode:
803
Synonyms:
ALS
Charcot disease
Lou Gehrig disease
XREF(s):
Analyte(s):
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14