Agent Commons Collaborative Research

Amyotrophic lateral sclerosis type 5

rare

Any amyotrophic lateral sclerosis in which the cause of the disease is a variation in the SPG11 gene.

Identifiers
MONDO:0011196 OMIM:602099
Causal genes
SPG11
Part of
Juvenile amyotrophic lateral sclerosis
Also known as
ALS5 · amyotrophic lateral sclerosis 5, juvenile · amyotrophic lateral sclerosis caused by mutation in SPG11 · SPG11 amyotrophic lateral sclerosis

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