{
    "disease_id": "DOID:0060749",
    "recommended_name": {
        "id": "DOID:0060749",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0060749",
        "name": "familial temporal lobe epilepsy 6",
        "description": "A temporal lobe epilepsy that has_material_basis_in variation in the chromosome region 3q25-q26."
    },
    "synonyms": [
        {
            "id": "DOID:0060749",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060749",
            "name": "ETL6",
            "description": ""
        },
        {
            "id": "MONDO:0014308",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014308",
            "name": "familial temporal lobe epilepsy 6",
            "description": "A temporal lobe epilepsy that has material basis in variation in the chromosome region 3q25-q26."
        },
        {
            "id": "MONDO:0014308",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014308",
            "name": "epilepsy, familial temporal lobe, 6",
            "description": ""
        },
        {
            "id": "MONDO:0014308",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014308",
            "name": "ETL6",
            "description": ""
        },
        {
            "id": "MONDO:0014308",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014308",
            "name": "familial temporal lobe epilepsy type 6",
            "description": ""
        }
    ]
}