{
    "disease_id": "DOID:0080394",
    "recommended_name": {
        "id": "DOID:0080394",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0080394",
        "name": "nephrotic syndrome type 19",
        "description": "A familial nephrotic syndrome that has_material_basis_in compound heterozygous mutation in the NUP160 gene on chromosome 11p11."
    },
    "synonyms": [
        {
            "id": "MONDO:0032582",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0032582",
            "name": "nephrotic syndrome, type 19",
            "description": ""
        },
        {
            "id": "MONDO:0032582",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0032582",
            "name": "NEPHROTIC SYNDROME, TYPE 19",
            "description": ""
        },
        {
            "id": "MONDO:0032582",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0032582",
            "name": "NPHS19",
            "description": ""
        },
        {
            "id": "MIM:618178",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/618178",
            "name": "Nephrotic syndrome 19",
            "description": "Nephrotic syndrome 19"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0080394"
    ],
    "unlinked_id_list": []
}