{
    "disease_id": "DOID:14784",
    "recommended_name": {
        "id": "DOID:14784",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:14784",
        "name": "olivopontocerebellar atrophy",
        "description": "A neurodegenerative disease that is characterized by progressive cerebellar ataxia, leading to clumsiness in body movements, veering from midline when walking, wide-based stance, and falls without signs of paralysis or weakness and has_material_basis_in expansion of CAG triplet repeats (glutamine) resulting in degeneration of neuron in the cerebellum, pons and inferior olives."
    },
    "synonyms": [
        {
            "id": "DOID:14784",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:14784",
            "name": "Dejerine-Thomas syndrome",
            "description": ""
        },
        {
            "id": "DOID:14784",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:14784",
            "name": "Thomas' syndrome",
            "description": ""
        },
        {
            "id": "DOID:14784",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:14784",
            "name": "WADIA-SWAMI SYNDROME",
            "description": ""
        }
    ]
}