{
    "disease_id": "DOID:0080385", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014752", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014752", 
            "name": "nephrotic syndrome, type 11"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014752", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014752", 
            "name": "nephrotic syndrome, type 11; NPHS11"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014752", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014752", 
            "name": "familial nephrotic syndrome caused by mutation in Nup107"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014752", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014752", 
            "name": "NPHS11"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014752", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014752", 
            "name": "NUP107 familial nephrotic syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080385", 
        "description": "A familial nephrotic syndrome characterized by onset in the first decade of life of steroid resistant progressive renal disease that has_material_basis_in homozygous or compound heterozygous mutation in the NUP107 gene on chromosome 12q15.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080385", 
        "name": "nephrotic syndrome type 11"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0080385#disease-associations", 
            "id": "0080385", 
            "database": "Alliance of Genome Resources"
        }
    ]
}