{
    "disease_id": "DOID:0111325",
    "recommended_name": {
        "id": "DOID:0111325",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111325",
        "name": "juvenile myoclonic epilepsy 10",
        "description": "A juvenile myoclonic epilepsy that has_material_basis_in heterozygous mutation in ICK on chromosome 6p12.1."
    },
    "synonyms": [
        {
            "id": "DOID:0111325",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111325",
            "name": "EJM10",
            "description": ""
        },
        {
            "id": "MONDO:0060671",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0060671",
            "name": "epilepsy, juvenile myoclonic, susceptibility to, 10",
            "description": ""
        },
        {
            "id": "MONDO:0060671",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0060671",
            "name": "EJM10",
            "description": ""
        },
        {
            "id": "MONDO:0060671",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0060671",
            "name": "epilepsy, juvenile myoclonic, susceptibility to, 10; EJM10",
            "description": ""
        },
        {
            "id": "MIM:617924",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/617924",
            "name": "Juvenile myoclonic epilepsy 10",
            "description": "Juvenile myoclonic epilepsy 10"
        }
    ]
}