NPHS1, NPHS1 adhesion molecule, nephrin, 4868

N. diseases: 87; N. variants: 189
Disease: Nephrotic Syndrome ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0027726
Disease: Nephrotic Syndrome
Nephrotic Syndrome 		0.400 CausalMutation group CLINVAR Recurrence of proteinuria following renal transplantation in congenital nephrotic syndrome of the Finnish type. 16518627 2006
CUI: C0027726
Disease: Nephrotic Syndrome
Nephrotic Syndrome 		0.400 Therapeutic group RGD Glomerular abundance of nephrin and podocin in experimental nephrotic syndrome: different effects of antiproteinuric therapies. 15942045 2005
CUI: C0027726
Disease: Nephrotic Syndrome
Nephrotic Syndrome 		0.400 Biomarker group LHGDN Congenital nephrotic syndrome of the Finnish type in Italy: a molecular approach. 12495287 2003
CUI: C0027726
Disease: Nephrotic Syndrome
Nephrotic Syndrome 		0.400 Biomarker group HPO
CUI: C0027726
Disease: Nephrotic Syndrome
Nephrotic Syndrome 		0.400 GeneticVariation group BEFREE To determine the frequency of inherited NS, 62 cases (representing 49 families with NS) from Saudi Arabia were screened for mutations in NPHS1, NPHS2, LAMB2, PLCE1, CD2AP, MYO1E, WT1, PTPRO and Nei endonuclease VIII-like 1 (NEIL1). 23595123 2013
CUI: C0027726
Disease: Nephrotic Syndrome
Nephrotic Syndrome 		0.400 Biomarker group LHGDN Expression of nephrin, podocin, alpha-actinin, and WT1 in children with nephrotic syndrome. 12961083 2003