{
    "disease_id": "DOID:0060752", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013741", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013741", 
            "name": "ETL5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013741", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013741", 
            "name": "epilepsy, familial temporal lobe, 5; ETL5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013741", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013741", 
            "name": "familial temporal lobe epilepsy type 5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013741", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013741", 
            "name": "epilepsy, familial temporal lobe, 5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013741", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013741", 
            "name": "epilepsy, familial temporal lobe, type 5"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060752", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060752", 
            "name": "ETL5"
        }, 
        {
            "url": "https://www.omim.org/entry/614417", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:614417", 
            "name": "Epilepsy, familial temporal lobe, 5"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060752", 
        "description": "A temporal lobe epilepsy that has_material_basis_in heterozygous mutation in the CPA6 gene on chromosome 8q13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060752", 
        "name": "familial temporal lobe epilepsy 5"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/614417", 
            "id": "614417", 
            "database": "MIM"
        }
    ]
}