FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term nephrotic syndrome type 7 ID (Ontology) DOID:0080388 (Human Disease)
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.
Also Known As "Ig-mediated membranoproliferative glomerulonephritis" ; "Ig-mediated MPGN" ; "immunoglobulin-mediated membranoproliferative glomerulonephritis" (for all, see Synonyms field below)
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 Genes
 nephrotic syndrome type 7       1
 for disease ribbon | nephrotic syndrome type 7       1
 model of | nephrotic syndrome type 7       1
Spanning Tree (Parents/Children)
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monogenic disease
 |__familial nephrotic syndrome__
autosomal genetic disease        |
 |__autosomal recessive disease__|
nephrotic syndrome               |
 |__familial nephrotic syndrome__|
                                 nephrotic syndrome type 7  1 rec.
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Is a autosomal recessive disease
familial nephrotic syndrome
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Synonyms
  • "Ig-mediated membranoproliferative glomerulonephritis" EXACT
    "Ig-mediated MPGN" EXACT
    "immunoglobulin-mediated membranoproliferative glomerulonephritis" EXACT
    "Immunoglobulin-mediated MPGN" EXACT
    "nephrotic syndrome type 7 with membranoptoliferative glomerulonephritis" EXACT
Secondary IDs
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MIM:615008
ORDO:329903