Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3496337
Disease: Idiopathic Nephrotic Syndrome
Idiopathic Nephrotic Syndrome
0.320 Biomarker disease CTD_human Nephrin in experimental glomerular disease. 11012881 2000
CUI: C3496337
Disease: Idiopathic Nephrotic Syndrome
Idiopathic Nephrotic Syndrome
0.320 GeneticVariation disease BEFREE Patients with a single mutation in NPHS1 received a diagnosis before those with potentially nongenetic NS and had a good response to therapies.Renal function was normal in all cases. 19406966 2009
CUI: C3496337
Disease: Idiopathic Nephrotic Syndrome
Idiopathic Nephrotic Syndrome
0.320 GeneticVariation disease BEFREE The levels of Podocin, the gene mutated in autosomal recessive steroid-resistant nephrotic syndrome (NPHS2), and Nephrin, the gene mutated in congenital nephrotic syndrome of the Finnish type (NPHS1), are slightly reduced in kr(enu)/kr(enu) podocytes. 12217315 2002
CUI: C3496337
Disease: Idiopathic Nephrotic Syndrome
Idiopathic Nephrotic Syndrome
0.320 Biomarker disease CTD_human Cloning of rat nephrin: expression in developing glomeruli and in proteinuric states. 10792613 2000