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

10 clinical trials for this condition and its sub-types, 0 tagged with Amyotrophic lateral sclerosis type 15 itself.

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Part of

↑ Familial amyotrophic lateral sclerosis (29)

Including sub-types (10) Tagged with Amyotrophic lateral sclerosis type 15 (0)

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