| Metadata | |
|---|---|
| ID | DOID:0080388 |
| Name | nephrotic syndrome type 7 |
| 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 |
| Xrefs | |
| Subsets |
DO_rare_slim |
| 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] |
| Parent Relationships |