Source: CTD_human

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4488
Gene Symbol: MSX2
MSX2
CUI: C0376634
Disease: Craniofacial Abnormalities
Craniofacial Abnormalities 		0.320 Biomarker CTD_human Perinatal lethality and multiple craniofacial malformations in MSX2 transgenic mice. 9147639

1997