Spinocerebellar ataxia, autosomal recessive 28

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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
spinocerebellar ataxia, autosomal recessive 28
MONDO_0032923
THG1L Causal
30214071 27307223 37670026 31168944 33682303
ClinGen, Open Targets
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. Cerebellar 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.