charge syndrome Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A syndrome that is acterized by a pattern of congenital anomalies including choanal atresia and malformations of the heart, inner ear, and retina. (Human Disease Ontology, DOID_0050834)
Similar Terms
Downloads & Tools

Genes

1 genes associated with the disease charge syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
CHD7 chromodomain helicase DNA binding protein 7