EFNB1, ephrin B1, 1947

N. diseases: 134; N. variants: 19
Disease: Atrial Septal Defects ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0018817
Disease: Atrial Septal Defects
Atrial Septal Defects 		0.010 GeneticVariation group BEFREE Craniofrontonasal Syndrome: Atrial Septal Defect With a Novel EFNB1 Gene Mutation. 24919122 2015