{
    "disease_id": "DOID:0060944",
    "recommended_name": {
        "id": "DOID:0060944",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060944",
        "name": "episodic kinesigenic dyskinesia 3",
        "description": "A dystonia characterized by dystonia, chorea, athetosis, and other hyperkinetic movements that has_material_basis_in heterozygous mutation in the TMEM151A gene on chromosome 11q13."
    },
    "synonyms": [
        {
            "id": "MONDO:0859380",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0859380",
            "name": "episodic kinesigenic dyskinesia 3",
            "description": ""
        },
        {
            "id": "MIM:620245",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/620245",
            "name": "Episodic kinesigenic dyskinesia 3",
            "description": "Episodic kinesigenic dyskinesia 3"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0060944"
    ],
    "unlinked_id_list": []
}