Spinocerebellar ataxia, autosomal recessive 13

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Subtype of: Autosomal recessive ataxia · Spinocerebellar ataxia · Spinocerebellar ataxia type 13
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Spinocerebellar ataxia, autosomal recessive 13
MONDO_0013905
GRM1 Unknown
36140834 31319223 22901947 26308914 28886343
Open Targets
All1 Causal0 Unknown1
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Chondromyxoid fibroma 1 shared geneGRM1 Related via 1 shared gene including GRM1. Congenital cerebellar ataxia 1 shared geneGRM1 Related via 1 shared gene including GRM1. Temporal lobe epilepsy 1 shared geneGRM1 Related via 1 shared gene including GRM1. Status epilepticus 1 shared geneGRM1 Related via 1 shared gene including GRM1. Spinocerebellar ataxia 1 shared geneGRM1 Related via 1 shared gene including GRM1.