Autosomal recessive spinocerebellar ataxia 18

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Subtype of: Autosomal recessive ataxia · Spinocerebellar ataxia
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
autosomal recessive spinocerebellar ataxia 18
MONDO_0014530
GRID2 Causal
35882834 21460832 25841024 37944084 9285588 24078737 23611888
Open Targets
All1 Causal1 Unknown1
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Congenital cerebellar ataxia 1 shared geneGRID2 Related via 1 shared gene including GRID2. Spinocerebellar ataxia 1 shared geneGRID2 Related via 1 shared gene including GRID2. Non-melanoma skin carcinoma 1 shared geneGRID2 Related via 1 shared gene including GRID2. Peripheral neuropathy 1 shared geneGRID2 Related via 1 shared gene including GRID2. Obsessive-compulsive disorder 1 shared geneGRID2 Related via 1 shared gene including GRID2.