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Spastic ataxia 3

MONDO:0012664

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

Also known as: ARSAL, MARS2 autosomal recessive spastic ataxia, SPAX3, autosomal recessive spastic ataxia caused by mutation in MARS2, autosomal recessive spastic ataxia type 3, spastic ataxia type 3, autosomal recessive spastic ataxia with leukoencephalopathy, spastic ataxia 3, autosomal recessive

14 clinical trials for this condition and its sub-types, 0 tagged with Spastic ataxia 3 itself.

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↑ Mitochondrial oxidative phosphorylation disorder (58) ↑ Autosomal recessive spastic ataxia (1)

Including sub-types (14) Tagged with Spastic ataxia 3 (0)

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