WNT9A, Wnt family member 9A, 7483

N. diseases: 17; N. variants: 2
Disease: Congenital anomaly of joint ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0521546
Disease: Congenital anomaly of joint
Congenital anomaly of joint 		0.010 Biomarker group BEFREE Because these WNT gene clusters might be fragile sites in the human genome, implication of WNT3 or WNT3A in cancer as well as implication of WNT14 or WNT14B in connective tissue disease and congenital joint malformation should be elucidated in the future. 12011973 2002