FOXG1 disorder
ICD-10 Code
F84.8
FOXG1 disorder
Definition
A monogenic disease that has material basis in mutation in the FOXG1 gene.
Also known as FOXG1 disorder, FOXG1 inherited genetic disease, FOXG1 syndrome, FOXG1 syndrome due to intragenic alteration, FOXG1-related epileptic-dyskinetic encephalopathy, inherited genetic disease caused by mutation in FOXG1, Rett syndrome, congenital variant — per MONDO