{
    "disease_id": "DOID:0060966",
    "recommended_name": {
        "id": "DOID:0060966",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060966",
        "name": "dystonia 22, juvenile-onset",
        "description": "A dystonia characterized by progressive, generalized dystonia associated with cognitive decline and cerebellar atrophy on brain imaging that has_material_basis_in homozygous loss-of-function mutation in the TSPOAP1 gene (610764) on chromosome 17q22."
    },
    "synonyms": [
        {
            "id": "MONDO:0957539",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0957539",
            "name": "dystonia 22, juvenile-onset",
            "description": ""
        },
        {
            "id": "MIM:620453",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/620453",
            "name": "Dystonia 22, juvenile-onset",
            "description": "Dystonia 22, juvenile-onset"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0060966"
    ],
    "unlinked_id_list": []
}