Source: BEFREE

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4488
Gene Symbol: MSX2
MSX2
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality 		0.020 Biomarker BEFREE BPP displayed the highest frequency of associated congenital defects (23.4%, vs HPP:6.6%, FPP: 15.4%). 9375922

1997
Entrez Id: 4488
Gene Symbol: MSX2
MSX2
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality 		0.020 Biomarker BEFREE Perinatal lethality and multiple craniofacial malformations in MSX2 transgenic mice. 9147639

1997