{
    "disease_id": "DOID:0110645", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013367", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013367", 
            "name": "long QT syndrome type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013367", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013367", 
            "name": "long QT syndrome 2; LQT2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013367", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013367", 
            "name": "long QT syndrome 1/2, digenic"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013367", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013367", 
            "name": "long QT syndrome 2/3, digenic"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013367", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013367", 
            "name": "long QT syndrome 2/5, digenic"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013367", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013367", 
            "name": "long QT syndrome 2, acquired, susceptibility to"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013367", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013367", 
            "name": "LQT2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013367", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013367", 
            "name": "long QT syndrome 2/9, digenic"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110645", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110645", 
            "name": "LQT2"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110645", 
        "description": "A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the KCNH2 gene on chromosome 7q36.1.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110645", 
        "name": "long QT syndrome 2"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110645#disease-associations", 
            "id": "0110645", 
            "database": "Alliance of Genome Resources"
        }
    ]
}