WNT3A, Wnt family member 3A, 89780

N. diseases: 141; N. variants: 5
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0264080
Disease: Juvenile osteoporosis
Juvenile osteoporosis
0.300 SusceptibilityMutation disease ORPHANET Rare variations in WNT3A and DKK1 may predispose carriers to primary osteoporosis. 22789636 2012