{
    "disease_id": "DOID:0081317",
    "recommended_name": {
        "id": "DOID:0081317",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0081317",
        "name": "multiple synostoses syndrome 1",
        "description": "A multiple synostoses syndrome 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 NOG gene on chromosome 17q22."
    },
    "synonyms": [
        {
            "id": "MONDO:0008519",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008519",
            "name": "multiple synostoses syndrome 1",
            "description": "Any multiple synostoses syndrome in which the cause of the disease is a mutation in the NOG gene."
        },
        {
            "id": "MONDO:0008519",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008519",
            "name": "NOG multiple synostoses syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008519",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008519",
            "name": "multiple synostoses syndrome 1",
            "description": ""
        },
        {
            "id": "MONDO:0008519",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008519",
            "name": "multiple synostoses syndrome caused by mutation in NOG",
            "description": ""
        },
        {
            "id": "MONDO:0008519",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008519",
            "name": "multiple synostoses syndrome caused by mutation in nog",
            "description": ""
        },
        {
            "id": "MONDO:0008519",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008519",
            "name": "multiple synostoses syndrome type 1",
            "description": ""
        },
        {
            "id": "MONDO:0008519",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008519",
            "name": "nog multiple synostoses syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008519",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008519",
            "name": "SYNS1",
            "description": ""
        },
        {
            "id": "MONDO:0008519",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008519",
            "name": "Wl syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008519",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008519",
            "name": "deafness-symphalangism syndrome of Herrmann",
            "description": ""
        },
        {
            "id": "MONDO:0008519",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008519",
            "name": "facioaudiosymphalangism syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008519",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008519",
            "name": "symphalangism brachydactyly syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008519",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008519",
            "name": "symphalangism-brachydactyly syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008519",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008519",
            "name": "synostoses multiple with brachydactyly",
            "description": ""
        },
        {
            "id": "MONDO:0008519",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008519",
            "name": "synostoses, multiple, with brachydactyly",
            "description": ""
        },
        {
            "id": "MIM:186500",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/186500",
            "name": "Multiple synostoses syndrome 1",
            "description": "Multiple synostoses syndrome 1"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0081317"
    ],
    "unlinked_id_list": []
}