Megalencephaly Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Enlargement of all or parts of the cerebral hemispheres. (Human Phenotype Ontology, HP_0001355)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D058627
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Genes

1 genes/proteins associated with the disease Megalencephaly from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
CHD8 chromodomain helicase DNA binding protein 8 2.88009