Cree leukoencephalopathy

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
CREE LEUKOENCEPHALOPATHY
99854
EIF2B1 Unknown
15136673 20301435
Orphanet
EIF2B2 Unknown
15136673 20301435
Orphanet
EIF2B3 Unknown
15136673 20301435
Orphanet
EIF2B4 Unknown
15136673 20301435
Orphanet
EIF2B5 Unknown
15136673 20301435
Orphanet
All5 Causal0 Unknown5
Related Diseases Diseases that share the most curated genes with Cree leukoencephalopathy.
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Congenital or early infantile cach syndrome 5 shared genesEIF2B3, EIF2B1, EIF2B2, EIF2B4, EIF2B5 Related via 5 shared genes including EIF2B3, EIF2B1, EIF2B2. Vanishing white matter disease 5 shared genesEIF2B3, EIF2B1, EIF2B2, EIF2B4, EIF2B5 Related via 5 shared genes including EIF2B3, EIF2B1, EIF2B2. Childhood ataxia with cns hypomyelination 5 shared genesEIF2B3, EIF2B1, EIF2B2, EIF2B4, EIF2B5 Related via 5 shared genes including EIF2B3, EIF2B1, EIF2B2. leukoencephalopathy with vanishing white matter 3 1 shared geneEIF2B3 Related via 1 shared gene including EIF2B3. leukoencephalopathy with vanishing white matter 1 1 shared geneEIF2B1 Related via 1 shared gene including EIF2B1.