Amyotrophic lateral sclerosis type 20

MONDO:0014181

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

Also known as: ALS20, HNRNPA1 amyotrophic lateral sclerosis, amyotrophic lateral sclerosis 20, amyotrophic lateral sclerosis caused by mutation in HNRNPA1, amyotrophic lateral sclerosis type 20

10 clinical trials for this condition and its sub-types, 0 tagged with Amyotrophic lateral sclerosis type 20 itself.

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Where it sits in the disease tree

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Part of

↑ Familial amyotrophic lateral sclerosis (29)

Including sub-types (10) Tagged with Amyotrophic lateral sclerosis type 20 (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.