{
    "disease_id": "DOID:0070384",
    "recommended_name": {
        "id": "DOID:0070384",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070384",
        "name": "developmental and epileptic encephalopathy 98",
        "description": "A developmental and epileptic encephalopathy characterized by onset of seizures in the first decade associated with variable global developmental delay that has_material_basis_in heterozygous mutation in the ATP1A2 gene on chromosome 1q23."
    },
    "synonyms": [
        {
            "id": "DOID:0070384",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070384",
            "name": "DEE98",
            "description": ""
        },
        {
            "id": "DOID:0070384",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070384",
            "name": "early infantile epileptic encephalopathy 98",
            "description": ""
        },
        {
            "id": "MONDO:0030472",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030472",
            "name": "developmental and epileptic encephalopathy 98",
            "description": ""
        },
        {
            "id": "MONDO:0030472",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030472",
            "name": "DEE98",
            "description": ""
        },
        {
            "id": "MIM:619605",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/619605",
            "name": "Developmental and epileptic encephalopathy 98",
            "description": "Developmental and epileptic encephalopathy 98"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070384"
    ],
    "unlinked_id_list": []
}