{
    "disease_id": "DOID:0111317",
    "recommended_name": {
        "id": "DOID:0111317",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111317",
        "name": "idiopathic generalized epilepsy 2",
        "description": "An idiopathic generalized epilepsy that has_material_basis_in variation in a region on chromosome 14q23."
    },
    "synonyms": [
        {
            "id": "DOID:0111317",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111317",
            "name": "EIG2",
            "description": ""
        },
        {
            "id": "MONDO:0011753",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011753",
            "name": "EIG2",
            "description": ""
        },
        {
            "id": "MONDO:0011753",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011753",
            "name": "epilepsy, idiopathic generalized, susceptibility to, 2",
            "description": ""
        },
        {
            "id": "MONDO:0011753",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011753",
            "name": "epilepsy, idiopathic generalized, susceptibility to, locus on chromosome 14",
            "description": ""
        },
        {
            "id": "MONDO:0011753",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011753",
            "name": "epilepsy, idiopathic generalized, susceptibility to, 2; EIG2",
            "description": ""
        },
        {
            "id": "MONDO:0011753",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011753",
            "name": "EIG2",
            "description": ""
        }
    ]
}