leukoencephalopathy with vanishing white matter 5

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Leukoencephalopathy with vanishing white matter 5
EIF2B5 Causal
12707859 21484434 12325082 19158808 11704758 15776425
ClinGen
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with leukoencephalopathy with vanishing white matter 5.
4 View disease cluster →
Congenital or early infantile cach syndrome 1 shared geneEIF2B5 Related via 1 shared gene including EIF2B5. Cree leukoencephalopathy 1 shared geneEIF2B5 Related via 1 shared gene including EIF2B5. Vanishing white matter disease 1 shared geneEIF2B5 Related via 1 shared gene including EIF2B5. Childhood ataxia with cns hypomyelination 1 shared geneEIF2B5 Related via 1 shared gene including EIF2B5.