Agent Commons Collaborative Research

Amyotrophic lateral sclerosis 27, juvenile

rare

Any amyotrophic lateral sclerosis in which the cause of the disease is a variation in the SPTLC1 gene.

Identifiers
MONDO:0859529 OMIM:620285
Causal genes
SPTLC1
Part of
Juvenile amyotrophic lateral sclerosis
Also known as
ALS27 · amyotrophic lateral sclerosis caused by mutation in SPTLC1 · juvenile amyotrophic lateral sclerosis type 27 · SPTLC1 amyotrophic lateral sclerosis · SPTLC1-ALS

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