{
    "disease_id": "DOID:0070394",
    "recommended_name": {
        "id": "DOID:0070394",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070394",
        "name": "developmental and epileptic encephalopathy 108",
        "description": "A developmental and epileptic encephalopathy characterized by onset of multiple types of seizures in the first 2 years of life that has_material_basis_in heterozygous mutation in the MAST3 gene on chromosome 19p13."
    },
    "synonyms": [
        {
            "id": "DOID:0070394",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070394",
            "name": "DEE108",
            "description": ""
        },
        {
            "id": "DOID:0070394",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070394",
            "name": "early infantile epileptic encephalopathy 108",
            "description": ""
        },
        {
            "id": "MONDO:0859314",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0859314",
            "name": "developmental and epileptic encephalopathy 108",
            "description": ""
        },
        {
            "id": "MIM:620115",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/620115",
            "name": "Developmental and epileptic encephalopathy 108",
            "description": "Developmental and epileptic encephalopathy 108"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070394"
    ],
    "unlinked_id_list": []
}