Episodes of liver failure, peripheral neuropathy, cerebellar atrophy, and ataxia

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
episodes of liver failure, peripheral neuropathy, cerebellar atrophy, and ataxia
MONDO_0014744
SCYL1 Unknown
26581903
Open Targets —
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Episodes of liver failure, peripheral neuropathy, cerebellar atrophy, and ataxia.
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Spinocerebellar ataxia, autosomal recessive 21 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.