RETT SYNDROME, CONGENITAL VARIANT Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link http://ctdbase.org/detail.go?type=disease&acc=OMIM:613454
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Genes

1 genes/proteins associated with the disease RETT SYNDROME, CONGENITAL VARIANT from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
FOXG1 forkhead box G1 2.88009