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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)
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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory