Gene: NPHS1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4868
Gene Symbol: NPHS1
NPHS1 		0.110 GeneticVariation disease BEFREE Congenital nephrotic syndrome of the Finnish type (CNF or NPHS1) is an autosomal recessive kidney disorder resulting in severe proteinurea and renal dysfunction. 11726550 2001
Entrez Id: 4868
Gene Symbol: NPHS1
NPHS1 		0.110 Biomarker disease HPO