spinocerebellar ataxia, autosomal recessive 28

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
spinocerebellar ataxia, autosomal recessive 28
THG1L Causal
30214071 27307223 37670026 31168944 33682303
ClinGen
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with spinocerebellar ataxia, autosomal recessive 28.
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Spinocerebellar ataxia 1 shared geneTHG1L Related via 1 shared gene including THG1L. Kidney disease 1 shared geneTHG1L Related via 1 shared gene including THG1L. Neurodevelopmental disorder 1 shared geneTHG1L Related via 1 shared gene including THG1L.