{
    "disease_id": "DOID:0070445",
    "recommended_name": {
        "id": "DOID:0070445",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070445",
        "name": "early-onset dystonia and/or spastic paraplegia",
        "description": "A dystonia characterized by variable onset of dystonia, spasticity, or both that has_material_basis_in heterozygous mutation in the ATP5MC3 gene on chromosome 2q31.1."
    },
    "synonyms": [
        {
            "id": "MONDO:0859215",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0859215",
            "name": "dystonia, early-onset, and/or spastic paraplegia",
            "description": ""
        },
        {
            "id": "MIM:619681",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/619681",
            "name": "Dystonia, early-onset, and/or spastic paraplegia",
            "description": "Dystonia, early-onset, and/or spastic paraplegia"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070445"
    ],
    "unlinked_id_list": []
}