{
    "disease_id": "DOID:0061046",
    "recommended_name": {
        "id": "DOID:0061046",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0061046",
        "name": "autosomal dominant intellectual developmental disorder 73",
        "description": "An autosomal dominant intellectual developmental disorder characterized by impaired intellectual development that ranges from mild to severe, speech delay, behavioral abnormalities, and nonspecific dysmorphic facial features that has_material_basis_in heterozygous mutation in the TAF4 gene on chromosome 20q13."
    },
    "synonyms": [
        {
            "id": "MONDO:0957536",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0957536",
            "name": "intellectual developmental disorder, autosomal dominant 73",
            "description": ""
        },
        {
            "id": "MIM:620450",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/620450",
            "name": "Intellectual developmental disorder, autosomal dominant 73",
            "description": "Intellectual developmental disorder, autosomal dominant 73"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0061046"
    ],
    "unlinked_id_list": []
}