{
    "disease_id": "DOID:0111325", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0060671", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0060671", 
            "name": "epilepsy, juvenile myoclonic, susceptibility to, 10"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0060671", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0060671", 
            "name": "EJM10"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0060671", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0060671", 
            "name": "epilepsy, juvenile myoclonic, susceptibility to, 10; EJM10"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111325", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111325", 
            "name": "EJM10"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111325", 
        "description": "A juvenile myoclonic epilepsy that has_material_basis_in heterozygous mutation in ICK on chromosome 6p12.1.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111325", 
        "name": "juvenile myoclonic epilepsy 10"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111325#disease-associations", 
            "id": "0111325", 
            "database": "Alliance of Genome Resources"
        }
    ]
}