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

24 clinical trials for this condition and its sub-types.

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