{
    "disease_id": "DOID:0110652", 
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:0110652", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110652", 
            "name": "LQT11"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012738", 
            "description": "Any long QT syndrome in which the cause of the disease is a mutation in the AKAP9 gene.", 
            "resource": "MONDO", 
            "id": "MONDO:0012738", 
            "name": "long QT syndrome 11"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012738", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012738", 
            "name": "AKAP9 long QT syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012738", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012738", 
            "name": "LQT11"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012738", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012738", 
            "name": "long QT syndrome type 11"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012738", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012738", 
            "name": "long QT syndrome 11"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012738", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012738", 
            "name": "long QT syndrome caused by mutation in AKAP9"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012738", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012738", 
            "name": "long QT syndrome 11; LQT11"
        }, 
        {
            "url": "https://www.omim.org/entry/611820", 
            "description": "Long QT syndrome 11", 
            "resource": "MIM", 
            "id": "MIM:611820", 
            "name": "Long QT syndrome 11"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110652", 
        "description": "A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the AKAP9 gene on chromosome 7q21.2.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110652", 
        "name": "long QT syndrome 11"
    }
}