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Summary Literature (0)
DOID:1184 - nephrotic syndrome


Disease Ontology Definition:A nephrosis characterized by marked increase in glomerular protein permeability resulting in marked elevation of urine protein levels, hypoalbuminemia, hyperlipidemia, and hypercoagulability.

Synonyms: finnish congenital nephrosis

Xenbase Genes : wt1, nphs2, nphs1, coq8b, emp2, arhgdia, plce1, dgke, ptpro

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0005377 - nephrotic syndrome

MIM:
MIM:256300 - NEPHROTIC SYNDROME, TYPE 1; NPHS1
MIM:256370 - NEPHROTIC SYNDROME, TYPE 4; NPHS4
MIM:600995 - NEPHROTIC SYNDROME, TYPE 2; NPHS2
MIM:610725 - NEPHROTIC SYNDROME, TYPE 3; NPHS3
MIM:614196 - NEPHROTIC SYNDROME, TYPE 6; NPHS6
MIM:615008 - NEPHROTIC SYNDROME, TYPE 7; NPHS7
MIM:615244 - NEPHROTIC SYNDROME, TYPE 8; NPHS8
MIM:615573 - NEPHROTIC SYNDROME, TYPE 9; NPHS9
MIM:615861 - NEPHROTIC SYNDROME, TYPE 10; NPHS10

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): nephrosis (is_a)