Term Name:	nephrotic syndrome type 1
Synonyms:	Finnish congenital nephrosis
Definition:	A familial nephrotic syndrome characterized by prenatal onset of massive proteinuria followed by steroid resistant renal disease that has_material_basis_in homozygous or compound heterozygous mutation in the NPHS1 gene on chromosome 19q13.
Ontology:	Human Disease [DOID:0080390]   ( DOID:0080390 )