NPHS1, NPHS1 adhesion molecule, nephrin, 4868

N. diseases: 87; N. variants: 189
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 GeneticVariation group LHGDN The results demonstrate that NPHS1 and NPHS2 mutations are also present in Chinese sporadic NS patients, suggesting that genetic changes of nephrin and podocin may play pathogenetic roles in some patients with sporadic steroid resistant NS. 17211152 2007
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 LHGDN Expression of nephrin, podocin, alpha-actinin, and WT1 in children with nephrotic syndrome. 12961083 2003
CUI: C0027726
Disease: Nephrotic Syndrome
Nephrotic Syndrome
0.400 Biomarker group MGD
CUI: C0027726
Disease: Nephrotic Syndrome
Nephrotic Syndrome
0.400 Biomarker group HPO
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