Spinocerebellar ataxia, autosomal recessive 21

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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 21
MONDO_0014744
SCYL1 Unknown
29419818 17571074 26581903 30531813 33442927 30842961 30914295
Open Targets —
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Spinocerebellar ataxia, autosomal recessive 21.
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Episodes of liver failure, peripheral neuropathy, cerebellar atrophy, and ataxia 1 shared geneSCYL1 Related via 1 shared gene including SCYL1. Acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome 1 shared geneSCYL1 Related via 1 shared gene including SCYL1. Verloes-bourguignon syndrome 1 shared geneSCYL1 Related via 1 shared gene including SCYL1. Infantile liver failure 1 shared geneSCYL1 Related via 1 shared gene including SCYL1. Cholestasis 1 shared geneSCYL1 Related via 1 shared gene including SCYL1.