{
    "disease_id": "DOID:0110656", 
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:0110656", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110656", 
            "name": "LQT15"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014550", 
            "description": "Any long QT syndrome in which the cause of the disease is a mutation in the CALM2 gene.", 
            "resource": "MONDO", 
            "id": "MONDO:0014550", 
            "name": "long QT syndrome 15"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014550", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014550", 
            "name": "LQT15"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014550", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014550", 
            "name": "CALM2 long QT syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014550", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014550", 
            "name": "long QT syndrome 15; LQT15"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014550", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014550", 
            "name": "long QT syndrome caused by mutation in CALM2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014550", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014550", 
            "name": "long QT syndrome 15"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014550", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014550", 
            "name": "long QT syndrome type 15"
        }, 
        {
            "url": "https://www.omim.org/entry/616249", 
            "description": "Long QT syndrome 15", 
            "resource": "MIM", 
            "id": "MIM:616249", 
            "name": "Long QT syndrome 15"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110656", 
        "description": "A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the CALM2 gene on chromosome 2p21.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110656", 
        "name": "long QT syndrome 15"
    }
}