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spinocerebellar ataxia, autosomal recessive 23 | RareConnect | RareConnect.io

/autosomal recessive cerebellar ataxia - epilepsy - intellectual disability syndrome

/spinocerebellar ataxia, autosomal recessive 23

spinocerebellar ataxia, autosomal recessive 23

Rare Disease

MONDO:0014846

Also Known As

SCAR23autosomal recessive cerebellar ataxia - epilepsy - intellectual disability syndrome due to TUD deficiencyspinocerebellar ataxia autosomal recessive type 23spinocerebellar ataxia, autosomal recessive 23spinocerebellar ataxia, autosomal recessive type 23

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Associated Genes

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

OMIM

OMIM:616949 ↗

Orphanet

Orphanet:404493 ↗

GARD

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