WNT9A, Wnt family member 9A, 7483

N. diseases: 17; N. variants: 2
Disease: Hyperandrogenism ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0206081
Disease: Hyperandrogenism
Hyperandrogenism 		0.010 GeneticVariation disease BEFREE Null-association results of HOXA genes and Wnt5a, Wnt7a, and Wnt9a have been reported, while point mutations of the WNT4 gene point mutations have been associated with an MRKH-like syndrome characterized by Mullerian duct regression and hyperandrogenism. 28434104 2017