{
    "disease_id": "DOID:0060685",
    "recommended_name": {
        "id": "DOID:0060685",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060685",
        "name": "autosomal dominant nocturnal frontal lobe epilepsy 4",
        "description": "An autosomal dominant nocturnal frontal lobe epilepsy that has_material_basis_in heterozygous mutation in the CHRNA2 gene on chromosome 8p21."
    },
    "synonyms": [
        {
            "id": "DOID:0060685",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060685",
            "name": "ENFL4",
            "description": ""
        },
        {
            "id": "DOID:0060685",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060685",
            "name": "nocturnal frontal lobe epilepsy 4",
            "description": ""
        },
        {
            "id": "DOID:0060685",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060685",
            "name": "benign familial infantile seizures 6",
            "description": ""
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0060685"
    ],
    "unlinked_id_list": []
}