{
    "disease_id": "DOID:0060940",
    "recommended_name": {
        "id": "DOID:0060940",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060940",
        "name": "dystonia 33",
        "description": "A dystonia characterized by a neurologic disorder with onset of focal or generalized dystonia in the first decades of life (from early childhood to adolescence) that has_material_basis_in heterozygous mutation in the EIF2AK2 gene on chromosome 2p22."
    },
    "synonyms": [
        {
            "id": "MONDO:0030513",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030513",
            "name": "dystonia 33",
            "description": ""
        },
        {
            "id": "MONDO:0030513",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030513",
            "name": "DYT33",
            "description": ""
        },
        {
            "id": "MIM:619687",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/619687",
            "name": "Dystonia 33",
            "description": "Dystonia 33"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0060940"
    ],
    "unlinked_id_list": []
}