Disease: Nephrosis, congenital ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3501848
Disease: Nephrosis, congenital
Nephrosis, congenital 		0.010 GeneticVariation disease BEFREE Disruption of MAGI2-RapGEF2-Rap1 signaling contributes to podocyte dysfunction in congenital nephrotic syndrome caused by mutations in MAGI2. 31171376 2019