{
    "disease_id": "DOID:0050434", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008222", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008222", 
            "name": "long QT syndrome type 7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008222", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008222", 
            "name": "LQT7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008222", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008222", 
            "name": "Potassium-sensitive periodic paralysis, ventricular ectopy, and dysmorphic features"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008222", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008222", 
            "name": "long QT syndrome 7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008222", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008222", 
            "name": "periodic paralysis, Potassium-sensitive cardiodysrhythmic type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008222", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008222", 
            "name": "Andersen syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008222", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008222", 
            "name": "cardiodysrhythmic potassium-sensitive periodic paralysis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008222", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008222", 
            "name": "ATS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008222", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008222", 
            "name": "Andersen cardiodysrhythmic periodic paralysis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008222", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008222", 
            "name": "Potassium-sensitive cardiodysrhythmic type"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050434", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050434", 
            "name": "ANDERSEN CARDIODYSRHYTHMIC PERIODIC PARALYSIS"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050434", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050434", 
            "name": "Andersen syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050434", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050434", 
            "name": "LQT7"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050434", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050434", 
            "name": "Long QT syndrome 7"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050434", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050434", 
            "name": "Potassium-Sensitive Cardiodysrhythmic Type"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050434", 
        "description": "A long QT syndrome that has_material_basis_in autosomal dominant inheritance of a mutation in the KCNJ2 gene which disrupts the rhythm of the heart's lower chambers (ventricular arrhythmia) and results_in an unusually small lower jaw (micrognathia), low-set ears, and an abnormal curvature of the fingers called clinodactyly.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050434", 
        "name": "Andersen-Tawil syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0050434#disease-associations", 
            "id": "0050434", 
            "database": "Alliance of Genome Resources"
        }
    ]
}