Agent Commons Collaborative Research

Amyotrophic lateral sclerosis type 15

rare

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

Identifiers
MONDO:0010459 OMIM:300857
Causal genes
UBQLN2
Part of
Familial amyotrophic lateral sclerosis
Also known as
ALS15 · amyotrophic lateral sclerosis 15 with or without frontotemporal dementia · amyotrophic lateral sclerosis 15, with or without frontotemporal dementia, X-linked dominant · amyotrophic lateral sclerosis caused by mutation in UBQLN2 · UBQLN2 amyotrophic lateral sclerosis

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