Disease: Congenital cerebral hernia ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0014065
Disease: Congenital cerebral hernia
Congenital cerebral hernia 		0.010 GeneticVariation disease BEFREE The GRHL3 C67G missense variant may increase the risk for spina bifida and encephalocele phenotypes. 31332962 2019