{
    "disease_id": "DOID:0080272",
    "recommended_name": {
        "id": "DOID:0080272",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0080272",
        "name": "nephrotic syndrome type 16",
        "description": "A familial nephrotic syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the KANK2 gene on chromosome 19p13."
    },
    "synonyms": [
        {
            "id": "MONDO:0033280",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0033280",
            "name": "nephrotic syndrome 16",
            "description": ""
        },
        {
            "id": "MONDO:0033280",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0033280",
            "name": "nephrotic syndrome 16",
            "description": ""
        },
        {
            "id": "MONDO:0033280",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0033280",
            "name": "nephrotic syndrome, type 16",
            "description": ""
        },
        {
            "id": "MONDO:0033280",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0033280",
            "name": "NPHS16",
            "description": ""
        },
        {
            "id": "MIM:617783",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/617783",
            "name": "Nephrotic syndrome 16",
            "description": "Nephrotic syndrome 16"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0080272"
    ],
    "unlinked_id_list": []
}