FOXG1, forkhead box G1, 2290

N. diseases: 224; N. variants: 51
Disease: Chorea ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0008489
Disease: Chorea
Chorea 		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
CUI: C0008489
Disease: Chorea
Chorea 		0.110 Biomarker phenotype HPO