leukoencephalopathy with vanishing white matter Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.omim.org/entry/603896
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Genes

4 genes associated with the leukoencephalopathy with vanishing white matter phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
EIF2B1 eukaryotic translation initiation factor 2B, subunit 1 alpha, 26kDa
EIF2B2 eukaryotic translation initiation factor 2B, subunit 2 beta, 39kDa
EIF2B3 eukaryotic translation initiation factor 2B, subunit 3 gamma, 58kDa
EIF2B5 eukaryotic translation initiation factor 2B, subunit 5 epsilon, 82kDa