Source: CTD_human

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 10683
Gene Symbol: DLL3
DLL3
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality 		0.330 Biomarker CTD_human Dll3 and Notch1 genetic interactions model axial segmental and craniofacial malformations of human birth defects. 17849441

2007