{
    "disease_id": "DOID:3535", 
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:3535", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:3535", 
            "name": "Unverricht - Lundborg disease"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:3535", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:3535", 
            "name": "Unverricht's disease"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:3535", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:3535", 
            "name": "Unverricht-Lundborg disease"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:3535", 
        "description": "A progressive myoclonus epilepsy characterized by onset between 6 and 13 years of age of action- and stimulus-sensitive myoclonus, tonic-clonic seizures with ataxia, and a mild cognitive decline.", 
        "resource": "Disease Ontology", 
        "id": "DOID:3535", 
        "name": "Unverricht-Lundborg syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/3535#disease-associations", 
            "id": "3535", 
            "database": "Alliance of Genome Resources"
        }
    ]
}