{
    "disease_id": "DOID:14784", 
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:14784", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:14784", 
            "name": "Dejerine-Thomas syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:14784", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:14784", 
            "name": "Thomas' syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:14784", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:14784", 
            "name": "WADIA-SWAMI SYNDROME"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:14784", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:14784", 
        "name": "olivopontocerebellar atrophy"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/14784#disease-associations", 
            "id": "14784", 
            "database": "Alliance of Genome Resources"
        }
    ]
}