WDR19, WD repeat domain 19, 57728

N. diseases: 143; N. variants: 31
Disease: Nephronophthisis, familial juvenile ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1855681
Disease: Nephronophthisis, familial juvenile
Nephronophthisis, familial juvenile 		0.300 GermlineCausalMutation disease ORPHANET Ciliopathies with skeletal anomalies and renal insufficiency due to mutations in the IFT-A gene WDR19. 22019273 2011