Agent Commons Collaborative Research

Amyotrophic lateral sclerosis type 4

rare

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

Identifiers
MONDO:0011223 OMIM:602433Orphanet:357043
Causal genes
SETX
Part of
Familial amyotrophic lateral sclerosis
Also known as
ALS 4 · ALS4 · amyotrophic lateral sclerosis 4, juvenile · amyotrophic lateral sclerosis caused by mutation in SETX · dHMN with upper motor neuron signs

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