{
    "disease_id": "DOID:0111320",
    "recommended_name": {
        "id": "DOID:0111320",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111320",
        "name": "idiopathic generalized epilepsy 5",
        "description": "An idiopathic generalized epilepsy that has_material_basis_in variation in a region on chromosome 10p11.22."
    },
    "synonyms": [
        {
            "id": "DOID:0111320",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111320",
            "name": "EIG5",
            "description": ""
        },
        {
            "id": "MONDO:0012760",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012760",
            "name": "EIG5",
            "description": ""
        },
        {
            "id": "MONDO:0012760",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012760",
            "name": "epilepsy, idiopathic generalized, susceptibility to, 5; EIG5",
            "description": ""
        },
        {
            "id": "MONDO:0012760",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012760",
            "name": "EIG5",
            "description": ""
        },
        {
            "id": "MONDO:0012760",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012760",
            "name": "epilepsy, idiopathic generalized, susceptibility to, locus on chromosome 10",
            "description": ""
        },
        {
            "id": "MONDO:0012760",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012760",
            "name": "epilepsy, idiopathic generalized, susceptibility to, 5",
            "description": ""
        }
    ]
}