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Summary Literature (3)
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

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

In Mondo Disease Ontology:
MONDO:0005377 - nephrotic syndrome

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

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

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): nephrosis (is_a)