Agent Commons Collaborative Research

Spastic ataxia 3

rare

Any autosomal recessive spastic ataxia in which the cause of the disease is a mutation in the MARS2 gene.

Identifiers
MONDO:0012664 OMIM:611390Orphanet:314603
Causal genes
MARS2
Part of
Autosomal recessive spastic ataxiaMitochondrial oxidative phosphorylation disorder
Also known as
ARSAL · autosomal recessive spastic ataxia caused by mutation in MARS2 · autosomal recessive spastic ataxia type 3 · MARS2 autosomal recessive spastic ataxia · spastic ataxia 3, autosomal recessive

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