Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4706552
Disease: Familial vesicoureteral reflux
Familial vesicoureteral reflux
0.300 GermlineCausalMutation disease ORPHANET Mutations in SOX17 are associated with congenital anomalies of the kidney and the urinary tract. 20960469 2010