{
    "disease_id": "DOID:0111693",
    "recommended_name": {
        "id": "DOID:0111693",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111693",
        "name": "familial adult myoclonic epilepsy 4",
        "description": "A familial adult myoclonic epilepsy that has_material_basis_in heterozygous mutation in the YEATS2 gene on chromosome 3q27.1."
    },
    "synonyms": [
        {
            "id": "DOID:0111693",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111693",
            "name": "FAME4",
            "description": ""
        },
        {
            "id": "DOID:0111693",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111693",
            "name": "FCMTE4",
            "description": ""
        },
        {
            "id": "DOID:0111693",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111693",
            "name": "familial cortical myoclonic tremor and epilepsy 4",
            "description": ""
        },
        {
            "id": "MONDO:0014055",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014055",
            "name": "epilepsy, familial adult myoclonic, 4",
            "description": ""
        },
        {
            "id": "MONDO:0014055",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014055",
            "name": "FAME4",
            "description": ""
        },
        {
            "id": "MONDO:0014055",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014055",
            "name": "epilepsy, myoclonic, familial adult, 4",
            "description": ""
        },
        {
            "id": "MONDO:0014055",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014055",
            "name": "epilepsy, familial ADULT myoclonic, 4",
            "description": ""
        },
        {
            "id": "MIM:615127",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/615127",
            "name": "Epilepsy, familial adult myoclonic, 4",
            "description": "Epilepsy, familial adult myoclonic, 4"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111693"
    ],
    "unlinked_id_list": []
}
