About   Help   FAQ
Disease Ontology Browser
nephrotic syndrome type 7 (DOID:0080388)
Alliance: disease page
Synonyms: Ig-mediated membranoproliferative glomerulonephritis; Ig-mediated MPGN; immunoglobulin-mediated membranoproliferative glomerulonephritis; Immunoglobulin-mediated MPGN; nephrotic syndrome type 7 with membranoptoliferative glomerulonephritis
Alt IDs: OMIM:615008, ORDO:329903
Definition: A familial nephrotic syndrome characterized by onset in the first decade of life of progressive renal disease with proteinuria and membranoproliferative glomerulonephritis that has_material_basis_in homozygous or compound heterozygous mutation in the DGKE gene on chromosome 17q22.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
02/18/2020
MGI 6.14
The Jackson Laboratory