Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 5210
Gene Symbol: PFKFB4
PFKFB4
CUI: C1837249
Disease: Malformations of Cortical Development, Group II
Malformations of Cortical Development, Group II 		0.010 Biomarker BEFREE PFKFB4-depleted embryos fail to activate <i>n-cadherin</i> and late NC specifiers, and exhibit severe migration defects resulting in craniofacial defects. 29038306

2017