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 		0.110 GeneticVariation phenotype BEFREE Children with deletions or intragenic mutations of FOXG1 also have postnatal microcephaly, morphologic abnormalities of the corpus callosum, and choreiform movements. 24836831 2014
Entrez Id: 2290
Gene Symbol: FOXG1
FOXG1 		0.110 Biomarker phenotype HPO