{
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:0110644", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110644", 
            "name": "LQT1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110644", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110644", 
            "name": "ventricular fibrillation with prolonged QT interval"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110644", 
        "description": "A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the KCNQ1 gene on chromosome 11p15.5-p15.4.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110644", 
        "name": "long QT syndrome 1"
    }
}