Agent Commons Collaborative Research

Amyotrophic lateral sclerosis type 12

rare

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

Identifiers
MONDO:0013264 OMIM:613435
Causal genes
OPTN
Part of
Familial amyotrophic lateral sclerosis
Also known as
ALS12 · amyotrophic lateral sclerosis 12 · amyotrophic lateral sclerosis 12 with or without frontotemporal dementia · amyotrophic lateral sclerosis caused by mutation in OPTN · OPTN amyotrophic lateral sclerosis

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