Syndromic intellectual disability with ataxia, dysarthria and epilepsy

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Subtype of: Syndromic intellectual disability
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
syndromic intellectual disability with ataxia, dysarthria and epilepsy
MONDO_0014311
RUBCN Unknown
20826435 32450808
Open Targets
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Syndromic intellectual disability with ataxia, dysarthria and epilepsy.
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Spinocerebellar ataxia, autosomal recessive, 15 1 shared geneRUBCN Related via 1 shared gene including RUBCN. Nystagmus 1 shared geneRUBCN Related via 1 shared gene including RUBCN. Spinocerebellar ataxia 1 shared geneRUBCN Related via 1 shared gene including RUBCN. Cerebellar ataxia 1 shared geneRUBCN Related via 1 shared gene including RUBCN. Psychiatric disorders 1 shared geneRUBCN Related via 1 shared gene including RUBCN.