| Gene | Score gda | Association Type | Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||||
|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.300 | CausalMutation | phenotype | CLINVAR | NPHS2 (podicin) mutations in Turkish children with idiopathic nephrotic syndrome. | 17899208 | 2007 | ||||
|
0.300 | Biomarker | phenotype | RGD | Nephrin and podocin dissociate at the onset of proteinuria in experimental membranous nephropathy. | 15882266 | 2005 | ||||
|
0.300 | CausalMutation | phenotype | CLINVAR | Plasma membrane targeting of podocin through the classical exocytic pathway: effect of NPHS2 mutations. | 14675423 | 2004 | ||||
|
0.300 | CausalMutation | phenotype | CLINVAR | A novel NPHS2 gene mutation in Turkish children with familial steroid-resistant nephrotic syndrome. | 15504144 | 2004 | ||||
|
0.300 | CausalMutation | phenotype | CLINVAR | NPHS2 mutation analysis shows genetic heterogeneity of steroid-resistant nephrotic syndrome and low post-transplant recurrence. | 15253708 | 2004 | ||||
|
0.300 | CausalMutation | phenotype | CLINVAR | Patients with mutations in NPHS2 (podocin) do not respond to standard steroid treatment of nephrotic syndrome. | 14978175 | 2004 | ||||
|
0.300 | GeneticVariation | phenotype | CLINVAR | |||||||
|
0.300 | Biomarker | phenotype | HPO |