{
    "disease_id": "DOID:0081319",
    "recommended_name": {
        "id": "DOID:0081319",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0081319",
        "name": "multiple synostoses syndrome 3",
        "description": "A multiple synostoses syndrome that is characterized by multiple joint fusions, usually commencing in the hands, conductive deafness, and characteristic facial features, including a broad, tubular-shaped nose and a thin upper vermilion and that has_material_basis_in heterozygous mutation in the FGF9 gene on chromosome 13q12."
    },
    "synonyms": [
        {
            "id": "MONDO:0013064",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013064",
            "name": "multiple synostoses syndrome 3",
            "description": "Any multiple synostoses syndrome in which the cause of the disease is a mutation in the FGF9 gene."
        },
        {
            "id": "MONDO:0013064",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013064",
            "name": "FGF9 multiple synostoses syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0013064",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013064",
            "name": "multiple synostoses syndrome 3",
            "description": ""
        },
        {
            "id": "MONDO:0013064",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013064",
            "name": "multiple synostoses syndrome caused by mutation in FGF9",
            "description": ""
        },
        {
            "id": "MONDO:0013064",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013064",
            "name": "multiple synostoses syndrome type 3",
            "description": ""
        },
        {
            "id": "MONDO:0013064",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013064",
            "name": "SYNS3",
            "description": ""
        },
        {
            "id": "MIM:612961",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/612961",
            "name": "Multiple synostoses syndrome 3",
            "description": "Multiple synostoses syndrome 3"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0081319"
    ],
    "unlinked_id_list": []
}