{
    "disease_id": "DOID:0060679", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014191", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014191", 
            "name": "catecholaminergic polymorphic ventricular tachycardia type 5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014191", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014191", 
            "name": "CPVT5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014191", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014191", 
            "name": "ventricular tachycardia, catecholaminergic polymorphic, 5, with or without muscle weakness; CPVT5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014191", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014191", 
            "name": "ventricular tachycardia, catecholaminergic polymorphic, 5, with or without muscle weakness"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014191", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014191", 
            "name": "TRDN catecholaminergic polymorphic ventricular tachycardia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014191", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014191", 
            "name": "catecholaminergic polymorphic ventricular tachycardia caused by mutation in TRDN"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014191", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014191", 
            "name": "CVPT5"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060679", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060679", 
            "name": "CVPT5"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060679", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060679", 
        "name": "catecholaminergic polymorphic ventricular tachycardia 5"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060679#disease-associations", 
            "id": "0060679", 
            "database": "Alliance of Genome Resources"
        }
    ]
}