{
    "disease_id": "DOID:0070385",
    "recommended_name": {
        "id": "DOID:0070385",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070385",
        "name": "developmental and epileptic encephalopathy 99",
        "description": "A developmental and epileptic encephalopathy characterized by onset of seizures in early childhood that has_material_basis_in heterozygous mutation in the ATP1A3 gene on chromosome 19q13."
    },
    "synonyms": [
        {
            "id": "DOID:0070385",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070385",
            "name": "DEE99",
            "description": ""
        },
        {
            "id": "DOID:0070385",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070385",
            "name": "early infantile epileptic encephalopathy 99",
            "description": ""
        },
        {
            "id": "MONDO:0030473",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030473",
            "name": "developmental and epileptic encephalopathy 99",
            "description": ""
        },
        {
            "id": "MONDO:0030473",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030473",
            "name": "DEE99",
            "description": ""
        },
        {
            "id": "MIM:619606",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/619606",
            "name": "Developmental and epileptic encephalopathy 99",
            "description": "Developmental and epileptic encephalopathy 99"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070385"
    ],
    "unlinked_id_list": []
}