Amyotrophic lateral sclerosis type 12

MONDO:0013264

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

Also known as: ALS12, OPTN amyotrophic lateral sclerosis, amyotrophic lateral sclerosis 12, amyotrophic lateral sclerosis 12 with or without frontotemporal dementia, amyotrophic lateral sclerosis caused by mutation in OPTN, amyotrophic lateral sclerosis type 12

10 clinical trials for this condition and its sub-types, 0 tagged with Amyotrophic lateral sclerosis type 12 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 12 (0)

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