{
    "disease_id": "DOID:0061253",
    "recommended_name": {
        "id": "DOID:0061253",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0061253",
        "name": "neurodevelopmental disorder with speech delay, movement abnormalities, and seizures",
        "description": "An autosomal dominant intellectual developmental disorder characterized by motor delay with mildly delayed walking, variably impaired intellectual development with poor or absent speech, behavioral abnormalities, early-onset seizures, and movement abnormalities, including tremor, ataxia, and dyskinesias that has_material_basis_in heterozygous mutation in the UNC13A gene on chromosome 19p13."
    },
    "synonyms": [
        {
            "id": "MONDO:0980941",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0980941",
            "name": "neurodevelopmental disorder with speech delay, movement abnormalities, and seizures",
            "description": ""
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0061253"
    ],
    "unlinked_id_list": []
}