Nephrotic Syndrome Type 7
Disease ID: disease_node_19078
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| Dbxref | MIM:615008, ORDO:329903 |
|---|---|
| Subclassof | DOID_2590, DOID_0050737 |
| Data Source | DOID |
| Synonyms | Ig-mediated MPGN, Ig-mediated membranoproliferative glomerulonephritis, Immunoglobulin-mediated MPGN, immunoglobulin-mediated membranoproliferative glomerulonephritis, nephrotic syndrome type 7 with membranoptoliferative glomerulonephritis |
| Doid Label | nephrotic syndrome type 7 |
| Doid Description | 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. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_19078 |
| Doid Id | DOID_0080388 |
| Label | Nephrotic Syndrome Type 7 |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease)