{
    "disease_id": "DOID:2843", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008646", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008646", 
            "name": "long QT syndrome 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008646", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008646", 
            "name": "Romano-Ward long QT syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008646", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008646", 
            "name": "long QT syndrome type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008646", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008646", 
            "name": "long QT syndrome 1/2, digenic"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008646", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008646", 
            "name": "long QT syndrome 1; LQT1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008646", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008646", 
            "name": "ventricular fibrillation with prolonged QT interval"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008646", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008646", 
            "name": "long QT syndrome 1, acquired, susceptibility to"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008646", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008646", 
            "name": "Ward-Romano syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008646", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008646", 
            "name": "LQT1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008646", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008646", 
            "name": "Romano-Ward syndrome"
        }, 
        {
            "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"
        }
    ], 
    "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"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/2843#disease-associations", 
            "id": "2843", 
            "database": "Alliance of Genome Resources"
        }
    ]
}