{
    "disease_id": "DOID:0080388",
    "recommended_name": {
        "id": "DOID:0080388",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0080388",
        "name": "nephrotic syndrome type 7",
        "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."
    },
    "synonyms": [
        {
            "id": "DOID:0080388",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0080388",
            "name": "Ig-mediated MPGN",
            "description": ""
        },
        {
            "id": "DOID:0080388",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0080388",
            "name": "Immunoglobulin-mediated MPGN",
            "description": ""
        },
        {
            "id": "DOID:0080388",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0080388",
            "name": "nephrotic syndrome type 7 with membranoptoliferative glomerulonephritis",
            "description": ""
        },
        {
            "id": "DOID:0080388",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0080388",
            "name": "immunoglobulin-mediated membranoproliferative glomerulonephritis",
            "description": ""
        },
        {
            "id": "DOID:0080388",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0080388",
            "name": "Ig-mediated membranoproliferative glomerulonephritis",
            "description": ""
        },
        {
            "id": "MONDO:0014005",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014005",
            "name": "immunoglobulin-mediated membranoproliferative glomerulonephritis",
            "description": "Glomerulonephritis characterized by mesangial proliferation, endocapillary proliferation, and glomerular capillary wall remodeling with immune complex deposits from classical complement pathway activation."
        },
        {
            "id": "MONDO:0014005",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014005",
            "name": "Ig-mediated MPGN",
            "description": ""
        },
        {
            "id": "MONDO:0014005",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014005",
            "name": "Ig-mediated membranoproliferative glomerulonephritis",
            "description": ""
        },
        {
            "id": "MONDO:0014005",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014005",
            "name": "NPHS7",
            "description": ""
        },
        {
            "id": "MONDO:0014005",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014005",
            "name": "immune complex mediated membranoproliferative glomerulonephritis",
            "description": ""
        },
        {
            "id": "MONDO:0014005",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014005",
            "name": "immunoglobulin-mediated MPGN",
            "description": ""
        },
        {
            "id": "MONDO:0014005",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014005",
            "name": "immunoglobulin-mediated membranoproliferative glomerulonephritis",
            "description": ""
        },
        {
            "id": "MONDO:0014005",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014005",
            "name": "membranoproliferative glomerulonephritis type I",
            "description": ""
        },
        {
            "id": "MONDO:0014005",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014005",
            "name": "mesangiocapillary glomerulonephritis type 1",
            "description": ""
        },
        {
            "id": "MONDO:0014005",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014005",
            "name": "nephrotic syndrome, type 7",
            "description": ""
        },
        {
            "id": "MONDO:0014005",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014005",
            "name": "nephrotic syndrome, type 7, with membranoproliferative glomerulonephritis",
            "description": ""
        },
        {
            "id": "MIM:615008",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/615008",
            "name": "Nephrotic syndrome 7",
            "description": "Nephrotic syndrome 7"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0080388"
    ],
    "unlinked_id_list": []
}