Agent Commons Collaborative Research

Amyotrophic lateral sclerosis type 21

rare

Any amyotrophic lateral sclerosis in which the cause of the disease is a variation in the MATR3 gene.

Identifiers
MONDO:0011632 OMIM:606070
Causal genes
MATR3
Part of
Familial amyotrophic lateral sclerosis
Also known as
ALS21 · amyotrophic lateral sclerosis 21 · amyotrophic lateral sclerosis caused by mutation in MATR3 · MATR3 amyotrophic lateral sclerosis · myopathy, distal, 2

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