{
    "disease_id": "DOID:0051089",
    "recommended_name": {
        "id": "DOID:0051089",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0051089",
        "name": "developmental and epileptic encephalopathy 120",
        "description": "A developmental and epileptic encephalopathy that is characterized by severe infantile epilepsy, developmental delay, and intellectual disability and that has_material_basis_in heterozygous mutation in the BAIAP2 gene on chromosome 17q25."
    },
    "synonyms": [
        {
            "id": "MONDO:0980948",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0980948",
            "name": "developmental and epileptic encephalopathy 120",
            "description": ""
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0051089"
    ],
    "unlinked_id_list": []
}