{
    "disease_id": "DOID:0070677",
    "recommended_name": {
        "id": "DOID:0070677",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070677",
        "name": "Ferguson-Bonni neurodevelopmental syndrome",
        "description": "A syndromic intellectual disability characterized by global developmental delay, impaired intellectual development, and hypotonia with early motor delay that has_material_basis_in homozygous mutation in the ANAPC7 gene on chromosome 12q24."
    },
    "synonyms": [
        {
            "id": "MONDO:0859220",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0859220",
            "name": "Ferguson-Bonni neurodevelopmental syndrome",
            "description": ""
        },
        {
            "id": "MIM:619699",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/619699",
            "name": "Ferguson-Bonni neurodevelopmental syndrome",
            "description": "Ferguson-Bonni neurodevelopmental syndrome"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070677"
    ],
    "unlinked_id_list": []
}