{
    "disease_id": "DOID:0050434",
    "recommended_name": {
        "id": "DOID:0050434",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0050434",
        "name": "Andersen-Tawil syndrome",
        "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."
    },
    "synonyms": [
        {
            "id": "DOID:0050434",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0050434",
            "name": "ANDERSEN CARDIODYSRHYTHMIC PERIODIC PARALYSIS",
            "description": ""
        },
        {
            "id": "DOID:0050434",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0050434",
            "name": "Andersen syndrome",
            "description": ""
        },
        {
            "id": "DOID:0050434",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0050434",
            "name": "LQT7",
            "description": ""
        },
        {
            "id": "DOID:0050434",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0050434",
            "name": "Long QT syndrome 7",
            "description": ""
        },
        {
            "id": "DOID:0050434",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0050434",
            "name": "Potassium-Sensitive Cardiodysrhythmic Type",
            "description": ""
        },
        {
            "id": "MONDO:0008222",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008222",
            "name": "Andersen-Tawil syndrome",
            "description": "Andersen's syndrome (AS) is a rare disorder characterized by periodic muscle paralysis, prolongation of the QT interval with a variety of ventricular arrhythmias (leading to predisposition to sudden cardiac death) and characteristic physical features: short stature, scoliosis, low-set ears, hypertelorism, broad nasal root, micrognathia, clinodactyly, brachydactyly and syndactyly."
        },
        {
            "id": "MONDO:0008222",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008222",
            "name": "ATS",
            "description": ""
        },
        {
            "id": "MONDO:0008222",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008222",
            "name": "Andersen cardiodysrhythmic periodic paralysis",
            "description": ""
        },
        {
            "id": "MONDO:0008222",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008222",
            "name": "Andersen syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008222",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008222",
            "name": "Andersen-Tawil syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008222",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008222",
            "name": "LQT7",
            "description": ""
        },
        {
            "id": "MONDO:0008222",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008222",
            "name": "Potassium-sensitive cardiodysrhythmic type",
            "description": ""
        },
        {
            "id": "MONDO:0008222",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008222",
            "name": "long QT syndrome 7",
            "description": ""
        },
        {
            "id": "MONDO:0008222",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008222",
            "name": "long QT syndrome type 7",
            "description": ""
        },
        {
            "id": "MONDO:0008222",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008222",
            "name": "Potassium-sensitive periodic paralysis, ventricular ectopy, and dysmorphic features",
            "description": ""
        },
        {
            "id": "MONDO:0008222",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008222",
            "name": "cardiodysrhythmic potassium-sensitive periodic paralysis",
            "description": ""
        },
        {
            "id": "MONDO:0008222",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008222",
            "name": "periodic paralysis, Potassium-sensitive cardiodysrhythmic type",
            "description": ""
        },
        {
            "id": "MIM:170390",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/170390",
            "name": "Long QT syndrome 7",
            "description": "Long QT syndrome 7"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0050434"
    ],
    "unlinked_id_list": []
}