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Autosomal recessive spinocerebellar ataxia 15
rareAny autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome in which the cause of the disease is a mutation in the RUBCN gene.
- Identifiers
- MONDO:0014311 OMIM:615705Orphanet:404499
- Causal genes
- RUBCN
- Also known as
- autosomal recessive cerebellar ataxia - epilepsy - intellectual disability syndrome caused by mutation in RUBCN · autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome caused by mutation in RUBCN · autosomal recessive spinocerebellar ataxia type 15 · RUBCN autosomal recessive cerebellar ataxia - epilepsy - intellectual disability syndrome · RUBCN autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome
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