Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2290
Gene Symbol: FOXG1
FOXG1
0.140 GeneticVariation disease BEFREE FOXG1-related disorders, caused by deletions, intragenic mutations or duplications, are usually associated with severe intellectual disability, autistic features, and, in 87% of subjects, epileptiform manifestations. 30639390 2019
Entrez Id: 2290
Gene Symbol: FOXG1
FOXG1
0.140 Biomarker disease BEFREE FOXG1-related disorders are associated with severe intellectual disability, absent speech with autistic features, and epilepsy. 24836831 2014
Entrez Id: 2290
Gene Symbol: FOXG1
FOXG1
0.140 Biomarker disease BEFREE FOXG1B (forkhead box G1B) is a very intriguing candidate gene since it is known to promote neuronal progenitor proliferation and to suppress premature neurogenesis and its disruption is reported in a patient with postnatal microcephaly, corpus callosum agenesis, seizures, and severe mental retardation. 18627055 2008
Entrez Id: 2290
Gene Symbol: FOXG1
FOXG1
0.140 GeneticVariation disease BEFREE Haploinsufficiency of novel FOXG1B variants in a patient with severe mental retardation, brain malformations and microcephaly. 16133170 2005
Entrez Id: 2290
Gene Symbol: FOXG1
FOXG1
0.140 GeneticVariation disease CLINVAR
Entrez Id: 2290
Gene Symbol: FOXG1
FOXG1
0.140 Biomarker disease HPO