{
    "disease_id": "DOID:0070533",
    "recommended_name": {
        "id": "DOID:0070533",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070533",
        "name": "long QT syndrome 16",
        "description": "A long QT syndrome characterized by perinatal onset of markedly prolonged corrected QT (QTc) interval, 2:1 atrioventricular (AV) block, and bradycardia or ventricular tachycardia (torsades de pointes) that has_material_basis_in heterozygous mutation in the CALM3 gene on chromosome 19q13.32. Syncope, cardiac arrest, and sudden death are common."
    },
    "synonyms": [
        {
            "id": "DOID:0070533",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070533",
            "name": "LQT16",
            "description": ""
        },
        {
            "id": "MONDO:0032915",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0032915",
            "name": "long QT syndrome 16",
            "description": ""
        },
        {
            "id": "MONDO:0032915",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0032915",
            "name": "long QT syndrome 16",
            "description": ""
        },
        {
            "id": "MONDO:0032915",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0032915",
            "name": "LQT16",
            "description": ""
        },
        {
            "id": "MIM:618782",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/618782",
            "name": "Long QT syndrome 16",
            "description": "Long QT syndrome 16"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070533"
    ],
    "unlinked_id_list": []
}