EFNB2, ephrin B2, 1948

N. diseases: 109; N. variants: 4
Disease: Anorectal Malformations ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3495676
Disease: Anorectal Malformations
Anorectal Malformations 		0.010 Biomarker group BEFREE Given the convincing argument for EFNB2 as a candidate gene for ARM, analyses of larger samples and screening of functionally relevant non-coding regions of EFNB2 are warranted. 24038947 2013