{
    "disease_id": "DOID:0050794",
    "recommended_name": {
        "id": "DOID:0050794",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0050794",
        "name": "multiple synostoses syndrome",
        "description": "A dysostosis that is characterized by premature joint ankylosis and has_material_basis_in autosomal dominant inhertitance."
    },
    "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": "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": "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": "multiple synostoses syndrome type 1",
            "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": "synostoses multiple with brachydactyly",
            "description": ""
        },
        {
            "id": "MONDO:0008519",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008519",
            "name": "multiple synostoses syndrome 1; SYNS1",
            "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": "multiple synostoses syndrome 1",
            "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": "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": "facioaudiosymphalangism syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0012394",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012394",
            "name": "multiple synostoses syndrome 2",
            "description": "Any multiple synostoses syndrome in which the cause of the disease is a mutation in the GDF5 gene."
        },
        {
            "id": "MONDO:0012394",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012394",
            "name": "multiple synostoses syndrome type 2",
            "description": ""
        },
        {
            "id": "MONDO:0012394",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012394",
            "name": "multiple synostoses syndrome 2; SYNS2",
            "description": ""
        },
        {
            "id": "MONDO:0012394",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012394",
            "name": "multiple synostoses syndrome 2",
            "description": ""
        },
        {
            "id": "MONDO:0012394",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012394",
            "name": "multiple synostoses syndrome caused by mutation in GDF5",
            "description": ""
        },
        {
            "id": "MONDO:0012394",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012394",
            "name": "GDF5 multiple synostoses syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0012394",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012394",
            "name": "SYNS2",
            "description": ""
        },
        {
            "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": "SYNS3",
            "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": "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 3",
            "description": ""
        },
        {
            "id": "MONDO:0013064",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013064",
            "name": "multiple synostoses syndrome 3; SYNS3",
            "description": ""
        },
        {
            "id": "MIM:186500",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/186500",
            "name": "Multiple synostoses syndrome 1",
            "description": "Multiple synostoses syndrome 1"
        },
        {
            "id": "MIM:610017",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/610017",
            "name": "Multiple synostoses syndrome 2",
            "description": "Multiple synostoses syndrome 2"
        },
        {
            "id": "MIM:612961",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/612961",
            "name": "Multiple synostoses syndrome 3",
            "description": "Multiple synostoses syndrome 3"
        }
    ]
}