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Summary Literature (0)
DOID:0080388 - nephrotic syndrome type 7

Disease Ontology 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.

Synonyms: Ig-mediated membranoproliferative glomerulonephritis, Ig-mediated MPGN, immunoglobulin-mediated membranoproliferative glomerulonephritis, Immunoglobulin-mediated MPGN, nephrotic syndrome type 7 with membranoptoliferative glomerulonephritis

Xenbase Genes : dgke


MIM:
MIM:615008 - NEPHROTIC SYNDROME, TYPE 7; NPHS7

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal recessive disease (is_a), familial nephrotic syndrome (is_a)