{
    "disease_id": "DOID:0060675",
    "recommended_name": {
        "id": "DOID:0060675",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060675",
        "name": "catecholaminergic polymorphic ventricular tachycardia 1",
        "description": "A catecholaminergic polymorphic ventricular tachycardia that is characterized by autosomal dominant inheritance and has_material_basis_in heterozygous mutation in the RYR2 gene on chromosome 1q43."
    },
    "synonyms": [
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            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060675",
            "name": "CVPT1",
            "description": ""
        },
        {
            "id": "DOID:0060675",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060675",
            "name": "arrhythmogenic right ventricular dysplasia 2",
            "description": ""
        },
        {
            "id": "MONDO:0011484",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011484",
            "name": "catecholaminergic polymorphic ventricular tachycardia 1",
            "description": "Polymorphic ventricular tachycardia induced by adrenergic stress. It is inherited in an autosomal dominant pattern and is caused by mutations in the ryanodine receptor 2 (RYR2) gene."
        },
        {
            "id": "MONDO:0011484",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011484",
            "name": "ARVC2",
            "description": ""
        },
        {
            "id": "MONDO:0011484",
            "resource": "MONDO",
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            "description": ""
        },
        {
            "id": "MONDO:0011484",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011484",
            "name": "RYR2 familial isolated arrhythmogenic right ventricular dysplasia",
            "description": ""
        },
        {
            "id": "MONDO:0011484",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011484",
            "name": "arrhythmogenic right ventricular cardiomyopathy 2",
            "description": ""
        },
        {
            "id": "MONDO:0011484",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011484",
            "name": "arrhythmogenic right ventricular dysplasia 2",
            "description": ""
        },
        {
            "id": "MONDO:0011484",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011484",
            "name": "arrhythmogenic right ventricular dysplasia type 2",
            "description": ""
        },
        {
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            "name": "arrhythmogenic right ventricular dysplasia, familial, type 2",
            "description": ""
        },
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            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011484",
            "name": "catecholaminergic polymorphic ventricular tachycardia 1",
            "description": ""
        },
        {
            "id": "MONDO:0011484",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011484",
            "name": "catecholaminergic polymorphic ventricular tachycardia type 1",
            "description": ""
        },
        {
            "id": "MONDO:0011484",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011484",
            "name": "familial arrhythmogenic right ventricular dysplasia 2",
            "description": ""
        },
        {
            "id": "MONDO:0011484",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011484",
            "name": "familial isolated arrhythmogenic right ventricular dysplasia caused by mutation in RYR2",
            "description": ""
        },
        {
            "id": "MONDO:0011484",
            "resource": "MONDO",
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            "name": "ventricular tachycardia, catecholaminergic polymorphic, 1",
            "description": ""
        },
        {
            "id": "MONDO:0011484",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011484",
            "name": "CPVT1",
            "description": ""
        },
        {
            "id": "MONDO:0011484",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011484",
            "name": "arrhythmogenic right ventricular dysplasia, familial, 2",
            "description": ""
        },
        {
            "id": "MONDO:0011484",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011484",
            "name": "ventricular tachycardia, catecholaminergic polymorphic, 1, with or without atrial dysfunction and/or dilated cardiomyopathy",
            "description": ""
        },
        {
            "id": "MONDO:0011484",
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            "url": "https://monarchinitiative.org/disease/MONDO:0011484",
            "name": "catecholaminergic polymorphic ventricular tachycardia 1",
            "description": "Polymorphic ventricular tachycardia induced by adrenergic stress. It is inherited in an autosomal dominant pattern and is caused by mutations in the ryanodine receptor 2 (RYR2) gene."
        },
        {
            "id": "MONDO:0011484",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011484",
            "name": "ARVC2",
            "description": ""
        },
        {
            "id": "MONDO:0011484",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011484",
            "name": "ARVD2",
            "description": ""
        },
        {
            "id": "MONDO:0011484",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011484",
            "name": "RYR2 familial isolated arrhythmogenic right ventricular dysplasia",
            "description": ""
        },
        {
            "id": "MONDO:0011484",
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            "url": "https://monarchinitiative.org/disease/MONDO:0011484",
            "name": "arrhythmogenic right ventricular cardiomyopathy 2",
            "description": ""
        },
        {
            "id": "MONDO:0011484",
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            "name": "arrhythmogenic right ventricular dysplasia 2",
            "description": ""
        },
        {
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            "name": "arrhythmogenic right ventricular dysplasia type 2",
            "description": ""
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        {
            "id": "MONDO:0011484",
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            "description": ""
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            "description": ""
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        {
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            "description": ""
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        {
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            "description": ""
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            "id": "MONDO:0011484",
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            "name": "familial isolated arrhythmogenic right ventricular dysplasia caused by mutation in RYR2",
            "description": ""
        },
        {
            "id": "MONDO:0011484",
            "resource": "MONDO",
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            "name": "ventricular tachycardia, catecholaminergic polymorphic, 1",
            "description": ""
        },
        {
            "id": "MONDO:0011484",
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            "name": "CPVT1",
            "description": ""
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            "description": ""
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        {
            "id": "MONDO:0011484",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011484",
            "name": "ventricular tachycardia, catecholaminergic polymorphic, 1, with or without atrial dysfunction and/or dilated cardiomyopathy",
            "description": ""
        },
        {
            "id": "MIM:604772",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/604772",
            "name": "Ventricular tachycardia, catecholaminergic polymorphic, 1, with or without atrial dysfunction and/or dilated cardiomyopathy",
            "description": "Ventricular tachycardia, catecholaminergic polymorphic, 1, with or without atrial dysfunction and/or dilated cardiomyopathy"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0060675"
    ],
    "unlinked_id_list": []
}
