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

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

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