Amyotrophic lateral sclerosis type 15

MONDO:0010459

Any amyotrophic lateral sclerosis in which the cause of the disease is a mutation in the UBQLN2 gene.

Also known as: ALS15, UBQLN2 amyotrophic lateral sclerosis, amyotrophic lateral sclerosis 15, with or without frontotemporal dementia, X-linked dominant, amyotrophic lateral sclerosis caused by mutation in UBQLN2, amyotrophic lateral sclerosis type 15, amyotrophic lateral sclerosis 15 with or without frontotemporal dementia

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

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