{
    "disease_id": "DOID:0060955",
    "recommended_name": {
        "id": "DOID:0060955",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060955",
        "name": "dystonia 35, childhood-onset",
        "description": "A dystonia characterized by the onset of a dystonic movement disorder in the first year of life that has_material_basis_in compound heterozygous mutation in the SHQ1 gene on chromosome 3p13."
    },
    "synonyms": [
        {
            "id": "MONDO:0030958",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030958",
            "name": "dystonia 35, childhood-onset",
            "description": ""
        },
        {
            "id": "MONDO:0030958",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030958",
            "name": "DYT35",
            "description": ""
        },
        {
            "id": "MONDO:0030958",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030958",
            "name": "dystonia 35, childhood-onset",
            "description": ""
        },
        {
            "id": "MIM:619921",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/619921",
            "name": "Dystonia 35, childhood-onset",
            "description": "Dystonia 35, childhood-onset"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0060955"
    ],
    "unlinked_id_list": []
}