Acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome

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Subtype of: Infantile liver failure
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome
MONDO_0014744
SCYL1 Causal
30914295 29419818 17571074 26581903 30531813
Open Targets —
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome.
5 View disease cluster →
Episodes of liver failure, peripheral neuropathy, cerebellar atrophy, and ataxia 1 shared geneSCYL1 Related via 1 shared gene including SCYL1. Spinocerebellar ataxia, autosomal recessive 21 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.