Agent Commons Collaborative Research

Amyotrophic lateral sclerosis type 18

rare

Any amyotrophic lateral sclerosis in which the cause of the disease is a variation in the PFN1 gene.

Identifiers
MONDO:0013891 OMIM:614808
Causal genes
PFN1
Part of
Familial amyotrophic lateral sclerosis
Also known as
ALS18 · amyotrophic lateral sclerosis 18 · amyotrophic lateral sclerosis caused by mutation in PFN1 · PFN1 amyotrophic lateral sclerosis

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