{
    "disease_id": "DOID:0111316",
    "recommended_name": {
        "id": "DOID:0111316",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111316",
        "name": "obsolete idiopathic generalized epilepsy 15",
        "description": "An idiopathic generalized epilepsy that has_material_basis_in heterozygous mutation in the RORB on chromosome 9q21.13."
    },
    "synonyms": [
        {
            "id": "MONDO:0032699",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0032699",
            "name": "epilepsy, idiopathic generalized, susceptibility to, 15",
            "description": ""
        },
        {
            "id": "MONDO:0032699",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0032699",
            "name": "EIG15",
            "description": ""
        },
        {
            "id": "MIM:618357",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/618357",
            "name": "Epilepsy, idiopathic generalized 15",
            "description": "Epilepsy, idiopathic generalized 15"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111316"
    ],
    "unlinked_id_list": []
}