Gene: FOXG1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2290
Gene Symbol: FOXG1
FOXG1 		0.410 GeneticVariation group BEFREE We recommend that patients with congenital RTT and Rett-like MR, especially those with brain malformations, such as hypoplasia of the corpus callosum, should be tested for FOXG1 mutations. 28851325 2017
Entrez Id: 2290
Gene Symbol: FOXG1
FOXG1 		0.410 Biomarker group CTD_human A 3 Mb deletion in 14q12 causes severe mental retardation, mild facial dysmorphisms and Rett-like features. 18627055 2008
Entrez Id: 2290
Gene Symbol: FOXG1
FOXG1 		0.410 Biomarker group HPO