Vanishing White Matter Leukodystrophy with Ovarian Failure Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:C565836
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Genes

5 genes/proteins associated with the disease Vanishing White Matter Leukodystrophy with Ovarian Failure from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
EIF2B4 eukaryotic translation initiation factor 2B, subunit 4 delta, 67kDa 2.88009
EIF2B5 eukaryotic translation initiation factor 2B, subunit 5 epsilon, 82kDa 2.88009
EIF2B2 eukaryotic translation initiation factor 2B, subunit 2 beta, 39kDa 2.88009
EIF2B3 eukaryotic translation initiation factor 2B, subunit 3 gamma, 58kDa 2.88009
EIF2B1 eukaryotic translation initiation factor 2B, subunit 1 alpha, 26kDa 2.88009