{
    "disease_id": "DOID:0080388", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014005", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014005", 
            "name": "immunoglobulin-mediated membranoproliferative glomerulonephritis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014005", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014005", 
            "name": "Mesangiocapillary glomerulonephritis type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014005", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014005", 
            "name": "Ig-mediated membranoproliferative glomerulonephritis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014005", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014005", 
            "name": "immune Complex mediated membranoproliferative glomerulonephritis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014005", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014005", 
            "name": "membranoproliferative glomerulonephritis type I"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014005", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014005", 
            "name": "Immunoglobulin-mediated MPGN"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014005", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014005", 
            "name": "NPHS7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014005", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014005", 
            "name": "nephrotic syndrome, type 7, with membranoproliferative glomerulonephritis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014005", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014005", 
            "name": "Ig-mediated MPGN"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014005", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014005", 
            "name": "nephrotic syndrome, type 7; NPHS7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014005", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014005", 
            "name": "nephrotic syndrome, type 7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014005", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014005", 
            "name": "hemolytic uremic syndrome, atypical, susceptibility to, 7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014005", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014005", 
            "name": "Ahus, susceptibility to, 7"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0080388", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0080388", 
            "name": "Ig-mediated MPGN"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0080388", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0080388", 
            "name": "Immunoglobulin-mediated MPGN"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0080388", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0080388", 
            "name": "nephrotic syndrome type 7 with membranoptoliferative glomerulonephritis"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0080388", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0080388", 
            "name": "immunoglobulin-mediated membranoproliferative glomerulonephritis"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0080388", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0080388", 
            "name": "Ig-mediated membranoproliferative glomerulonephritis"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080388", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080388", 
        "name": "nephrotic syndrome type 7"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0080388#disease-associations", 
            "id": "0080388", 
            "database": "Alliance of Genome Resources"
        }
    ]
}