WNT2B, Wnt family member 2B, 7482

N. diseases: 65; N. variants: 12
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
0.010 AlteredExpression group BEFREE Expression Analysis of ACSL5 and Wnt2B in Human Congenital Pulmonary Airway Malformations. 30463708 2018