{
    "disease_id": "DOID:0060679",
    "recommended_name": {
        "id": "DOID:0060679",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060679",
        "name": "catecholaminergic polymorphic ventricular tachycardia 5",
        "description": "A catecholaminergic polymorphic ventricular tachycardia that is characterized by autosomal recessive inheritance and has_material_basis_in homozygous or compound heterozygous mutation in the TRDN gene on chromosome 6q22."
    },
    "synonyms": [
        {
            "id": "DOID:0060679",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060679",
            "name": "CVPT5",
            "description": ""
        },
        {
            "id": "MONDO:0014191",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014191",
            "name": "catecholaminergic polymorphic ventricular tachycardia 5",
            "description": "Any catecholaminergic polymorphic ventricular tachycardia in which the cause of the disease is a mutation in the TRDN gene."
        },
        {
            "id": "MONDO:0014191",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014191",
            "name": "TRDN catecholaminergic polymorphic ventricular tachycardia",
            "description": ""
        },
        {
            "id": "MONDO:0014191",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014191",
            "name": "cardiac arrhythmia syndrome, with or without skeletal muscle weakness",
            "description": ""
        },
        {
            "id": "MONDO:0014191",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014191",
            "name": "catecholaminergic polymorphic ventricular tachycardia 5",
            "description": ""
        },
        {
            "id": "MONDO:0014191",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014191",
            "name": "catecholaminergic polymorphic ventricular tachycardia caused by mutation in TRDN",
            "description": ""
        },
        {
            "id": "MONDO:0014191",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014191",
            "name": "catecholaminergic polymorphic ventricular tachycardia type 5",
            "description": ""
        },
        {
            "id": "MONDO:0014191",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014191",
            "name": "CPVT5",
            "description": ""
        },
        {
            "id": "MONDO:0014191",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014191",
            "name": "ventricular tachycardia, catecholaminergic polymorphic, 5, with or without muscle weakness",
            "description": ""
        },
        {
            "id": "MIM:615441",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/615441",
            "name": "Cardiac arrhythmia syndrome, with or without skeletal muscle weakness",
            "description": "Cardiac arrhythmia syndrome, with or without skeletal muscle weakness"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0060679"
    ],
    "unlinked_id_list": []
}