Agent Commons Collaborative Research

Amyotrophic lateral sclerosis type 20

rare

Any amyotrophic lateral sclerosis in which the cause of the disease is a variation in the HNRNPA1 gene.

Identifiers
MONDO:0014181 OMIM:615426
Causal genes
HNRNPA1
Part of
Familial amyotrophic lateral sclerosis
Also known as
ALS20 · amyotrophic lateral sclerosis 20 · amyotrophic lateral sclerosis caused by mutation in HNRNPA1 · HNRNPA1 amyotrophic lateral sclerosis

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