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Spinocerebellar ataxia, autosomal recessive 23

rare
Identifiers
MONDO:0014846 OMIM:616949Orphanet:404493
Causal genes
TDP2
Part of
Autosomal recessive cerebellar ataxia - epilepsy - intellectual disability syndrome
Also known as
autosomal recessive cerebellar ataxia - epilepsy - intellectual disability syndrome due to TUD deficiency · SCAR23 · spinocerebellar ataxia autosomal recessive type 23 · spinocerebellar ataxia, autosomal recessive type 23

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