Source: CTD_human

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 93986
Gene Symbol: FOXP2
FOXP2
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		0.400 Biomarker CTD_human Absence of a paternally inherited FOXP2 gene in developmental verbal dyspraxia. 17033973

2006
Entrez Id: 93986
Gene Symbol: FOXP2
FOXP2
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		0.400 Biomarker CTD_human Our findings suggest that the FOXP2 gene may be involved in the pathogenesis of autism in Chinese population. 15108192

2004