OBO ID: DOID:0080388
Term Name: nephrotic syndrome type 7 Search Ontology:
Synonyms:
  • Ig-mediated membranoproliferative glomerulonephritis
  • Ig-mediated MPGN
  • immunoglobulin-mediated membranoproliferative glomerulonephritis
  • Immunoglobulin-mediated MPGN
  • nephrotic syndrome type 7 with membranoptoliferative glomerulonephritis
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. https://www.ncbi.nlm.nih.gov/pubmed/23274426
References:
Ontology: Human Disease   (DOID:0080388)
OTHER nephrotic syndrome type 7 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
DGKE {Hemolytic uremic syndrome, atypical, susceptibility to, 7} 615008
Nephrotic syndrome, type 7 615008
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None