{
    "disease_id": "DOID:0081320",
    "recommended_name": {
        "id": "DOID:0081320",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0081320",
        "name": "multiple synostoses syndrome 4",
        "description": "A multiple synostoses syndrome that is characterized by fusion of carpal and tarsal bones, as well as conductive hearing loss and that has_material_basis_in heterozygous mutation in the GDF6 gene on chromosome 8q22."
    },
    "synonyms": [
        {
            "id": "MONDO:0054752",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0054752",
            "name": "multiple synostoses syndrome 4",
            "description": ""
        },
        {
            "id": "MONDO:0054752",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0054752",
            "name": "multiple synostoses syndrome 4",
            "description": ""
        },
        {
            "id": "MONDO:0054752",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0054752",
            "name": "SYNS4",
            "description": ""
        },
        {
            "id": "MIM:617898",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/617898",
            "name": "Multiple synostoses syndrome 4",
            "description": "Multiple synostoses syndrome 4"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0081320"
    ],
    "unlinked_id_list": []
}