{
    "disease_id": "DOID:0111310",
    "recommended_name": {
        "id": "DOID:0111310",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111310",
        "name": "familial febrile seizures 2",
        "description": "A familial febrile seizures that has_material_basis_in variation in a region on chromosome 19p13.3."
    },
    "synonyms": [
        {
            "id": "DOID:0111310",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111310",
            "name": "FEB2",
            "description": ""
        },
        {
            "id": "DOID:0111310",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111310",
            "name": "familial febrile convulsions 2",
            "description": ""
        },
        {
            "id": "MONDO:0100519",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0100519",
            "name": "epilepsy, idiopathic generalized, susceptibility to, 17",
            "description": ""
        },
        {
            "id": "MONDO:0100519",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0100519",
            "name": "EIG17",
            "description": ""
        },
        {
            "id": "MIM:602477",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/602477",
            "name": "Epilepsy, idiopathic generalized 17",
            "description": "Epilepsy, idiopathic generalized 17"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111310"
    ],
    "unlinked_id_list": []
}