Summary Literature (4)

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

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

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee