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