{
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:2843", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2843", 
            "name": "LQT"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:2843", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2843", 
            "name": "Romano-Ward syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:2843", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2843", 
            "name": "long Q-T syndrome"
        }, 
        {
            "url": "https://www.omim.org/entry/192500", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:192500", 
            "name": "Long QT syndrome 1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:2843", 
        "description": "An autosomal genetic disease that is characterized by delayed repolarization of the heart following a heartbeat increases the risk of episodes of torsade de pointes (TDP, a form of irregular heartbeat that originates from the ventricles).", 
        "resource": "Disease Ontology", 
        "id": "DOID:2843", 
        "name": "long QT syndrome"
    }
}