Encephalopathy, Neonatal Severe, Due To Mecp2 Mutations 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:C566878
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Genes

1 genes/proteins associated with the disease Encephalopathy, Neonatal Severe, Due To Mecp2 Mutations from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
MECP2 methyl CpG binding protein 2 2.88009