Any amyotrophic lateral sclerosis in which the cause of the disease is a mutation in the ALS2 gene.
Comprehensive, easy-to-understand information about this condition
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Gene data from MyGene.info • Click to view on NCBI Gene
juvenile amyotrophic lateral sclerosis with dementia
MONDO:0008781
amyotrophic lateral sclerosis type 5
MONDO:0011196
juvenile primary lateral sclerosis
MONDO:0011663
infantile-onset ascending hereditary spastic paralysis
MONDO:0011797
amyotrophic lateral sclerosis type 16
MONDO:0013715