syndromic intellectual disability pervasive developmental disorder congenital nervous system disorder monogenic epilepsy atypical Rett syndrome FOXG1 disorder 2018-06-29T19:29:48Z https://github.com/monarch-initiative/mondo/issues/4069 https://github.com/monarch-initiative/mondo/issues/5588 https://github.com/monarch-initiative/mondo/issues/7850 https://github.com/monarch-initiative/mondo/issues/9285 https://www.malacards.org/card/foxg1_syndrome https://www.malacards.org/card/foxg1_syndrome_due_to_intragenic_alteration https://www.malacards.org/card/rett_syndrome_congenital_variant OMIM:613454 MONDO:0100040 MEDGEN:462055 FOXG1 disorder DOID:0070657 A monogenic disease that has material basis in mutation in the FOXG1 gene. FOXG1 inherited genetic disease Orphanet:561854 FOXG1-related epileptic-dyskinetic encephalopathy inherited genetic disease caused by mutation in FOXG1 NCIT:C176903 GARD:0026022 Rett syndrome, congenital variant UMLS:C3150705 ICD10CM:F84.8 Orphanet:598164 FOXG1 syndrome due to intragenic alteration FOXG1 syndrome Mendelian neurodevelopmental disorder