{
    "disease_id": "DOID:0080393", 
    "synonyms": [], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080393", 
        "description": "A familial nephrotic syndrome that has_material_basis_in by homozygous or compound heterozygous mutation in the NUP133 gene on chromosome 1q42.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080393", 
        "name": "nephrotic syndrome type 18"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0080393#disease-associations", 
            "id": "0080393", 
            "database": "Alliance of Genome Resources"
        }
    ]
}