Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1742
Gene Symbol: DLG4
DLG4
CUI: C0175702
Disease: Williams Syndrome
Williams Syndrome 		0.510 Biomarker CTD_human The study provides an initial link between human DLG4 gene variation and key neural endophenotypes of Williams' syndrome and perhaps corticoamygdala regulation of emotional and social processes more generally. 20952458

2010
Entrez Id: 1742
Gene Symbol: DLG4
DLG4
CUI: C0175702
Disease: Williams Syndrome
Williams Syndrome 		0.510 Biomarker MGD The study provides an initial link between human DLG4 gene variation and key neural endophenotypes of Williams' syndrome and perhaps corticoamygdala regulation of emotional and social processes more generally. 20952458

2010
Entrez Id: 1742
Gene Symbol: DLG4
DLG4
CUI: C0175702
Disease: Williams Syndrome
Williams Syndrome 		0.510 GeneticVariation BEFREE The study provides an initial link between human DLG4 gene variation and key neural endophenotypes of Williams' syndrome and perhaps corticoamygdala regulation of emotional and social processes more generally. 20952458

2010