DLG4, discs large MAGUK scaffold protein 4, 1742

N. diseases: 91; N. variants: 54
Disease: Williams Syndrome ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0175702
Disease: Williams Syndrome
Williams Syndrome 		0.510 Biomarker disease 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
CUI: C0175702
Disease: Williams Syndrome
Williams Syndrome 		0.510 Biomarker disease 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
CUI: C0175702
Disease: Williams Syndrome
Williams Syndrome 		0.510 GeneticVariation disease 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