{
    "disease_id": "DOID:0051090",
    "recommended_name": {
        "id": "DOID:0051090",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0051090",
        "name": "developmental and epileptic encephalopathy 121",
        "description": "A developmental and epileptic encephalopathy that is characterized by neonatal- or infantile-onset epilepsy, global developmental delay or intellectual disability, and death in infancy, childhood, or early adulthood and that has_material_basis_in homozygous mutation in the LGI1 gene on chromosome 10q23."
    },
    "synonyms": [
        {
            "id": "MONDO:0980966",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0980966",
            "name": "developmental and epileptic encephalopathy 121",
            "description": ""
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0051090"
    ],
    "unlinked_id_list": []
}