{
    "disease_id": "DOID:0061049",
    "recommended_name": {
        "id": "DOID:0061049",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0061049",
        "name": "autosomal dominant intellectual developmental disorder type FRA12A",
        "description": "An autosomal dominant intellectual developmental disorder that has_material_basis_in heterozygous expanded CGG repeat in the 5-prime untranslated region of the DIP2B gene on chromosome 12q13."
    },
    "synonyms": [
        {
            "id": "MONDO:0007634",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007634",
            "name": "intellectual disability, FRA12A type",
            "description": ""
        },
        {
            "id": "MONDO:0007634",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007634",
            "name": "intellectual disability, FRA12A type",
            "description": ""
        },
        {
            "id": "MONDO:0007634",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007634",
            "name": "mental retardation, FRA12A type",
            "description": ""
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0061049"
    ],
    "unlinked_id_list": []
}