XPNPEP3, X-prolyl aminopeptidase 3, 63929

N. diseases: 20; N. variants: 3
Disease: AURAL ATRESIA, CONGENITAL ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1842937
Disease: AURAL ATRESIA, CONGENITAL
AURAL ATRESIA, CONGENITAL 		0.010 GeneticVariation disease BEFREE These results identify APP 3'UTR sequence variants as genetic determinants of Aβ-CAA. 25828868 2016