Disease Summary help help Associated Targets (1)Tbio1 Explore Associated Targets list Mondo Description A monogenic disease that has material basis in mutation in the FOXG1 gene. Mondo Term and Equivalent IDs MONDO:0100040: FOXG1 disorder
Disease Hierarchy help helpParentsgenetic nervous system disorder (6096)Tbio4331Tchem803Tdark604Tclin358pervasive developmental disorder (864)Tbio581Tchem105Tdark93Tclin85syndromic intellectual disability (837)Tbio640Tchem110Tclin48Tdark39monogenic epilepsy (144)Tbio81Tclin33Tchem29Tdark1ChildrenRett syndrome, congenital variant (1)Tbio1