{
    "disease_id": "DOID:0080393",
    "recommended_name": {
        "id": "DOID:0080393",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0080393",
        "name": "nephrotic syndrome type 18",
        "description": "A familial nephrotic syndrome that has_material_basis_in by homozygous or compound heterozygous mutation in the NUP133 gene on chromosome 1q42."
    },
    "synonyms": [
        {
            "id": "MIM:618177",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/618177",
            "name": "Nephrotic syndrome 18",
            "description": "Nephrotic syndrome 18"
        }
    ]
}