{
    "disease_id": "DOID:0081397",
    "recommended_name": {
        "id": "DOID:0081397",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0081397",
        "name": "Vissers-Bodmer syndrome",
        "description": "A syndrome that is characterized by global developmental delay with variably impaired intellectual development, speech delay, motor delay, and behavioral abnormalities apparent from infancy and that has_material_basis_in heterozygous mutation in the CNOT1 gene on chromosome 16q21."
    },
    "synonyms": [
        {
            "id": "MONDO:0033618",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0033618",
            "name": "Vissers-Bodmer syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0033618",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0033618",
            "name": "VIBOS",
            "description": ""
        },
        {
            "id": "MIM:619033",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/619033",
            "name": "Vissers-Bodmer syndrome",
            "description": "Vissers-Bodmer syndrome"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0081397"
    ],
    "unlinked_id_list": []
}