{
    "disease_id": "DOID:0050561",
    "recommended_name": {
        "id": "DOID:0050561",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0050561",
        "name": "Lennox-Gastaut syndrome",
        "description": "A childhood electroclinical syndrome that is characterized by frequent seizures and intellectual disability that present in early childhood."
    },
    "synonyms": [
        {
            "id": "DOID:0050561",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0050561",
            "name": "Lennox syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0016532",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0016532",
            "name": "Lennox-Gastaut syndrome",
            "description": "Lennox-Gastaut syndrome (LGS) belongs to the group of severe childhood epileptic encephalopathies."
        },
        {
            "id": "MONDO:0016532",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0016532",
            "name": "LGS",
            "description": ""
        },
        {
            "id": "MONDO:0016532",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0016532",
            "name": "encephalopathy of childhood",
            "description": ""
        },
        {
            "id": "MONDO:0016532",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0016532",
            "name": "epileptic encephalopathy Lennox-Gastaut type",
            "description": ""
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0050561"
    ],
    "unlinked_id_list": []
}