{
    "disease_id": "DOID:0061038",
    "recommended_name": {
        "id": "DOID:0061038",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0061038",
        "name": "autosomal dominant intellectual developmental disorder 65",
        "description": "An autosomal dominant intellectual developmental disorder characterized by delayed motor and speech acquisition, variably impaired intellectual development, and behavioral abnormalities that has_material_basis_in heterozygous mutation in the KDM4B gene on chromosome 19p13."
    },
    "synonyms": [
        {
            "id": "MONDO:0023657",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0023657",
            "name": "intellectual developmental disorder, autosomal dominant 65",
            "description": ""
        },
        {
            "id": "MONDO:0023657",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0023657",
            "name": "MRD65",
            "description": ""
        },
        {
            "id": "MONDO:0023657",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0023657",
            "name": "mental retardation, autosomal dominant 65",
            "description": ""
        },
        {
            "id": "MIM:619320",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/619320",
            "name": "Intellectual developmental disorder, autosomal dominant 65",
            "description": "Intellectual developmental disorder, autosomal dominant 65"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0061038"
    ],
    "unlinked_id_list": []
}