{
    "disease_id": "DOID:0050431", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007152", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007152", 
            "name": "arrhythmogenic right ventricular dysplasia 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007152", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007152", 
            "name": "TGFB3 arrhythmogenic right ventricular cardiomyopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007152", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007152", 
            "name": "arrhythmogenic right ventricular cardiomyopathy 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007152", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007152", 
            "name": "Uhl anomaly"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007152", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007152", 
            "name": "arrhythmogenic right ventricular dysplasia, familial, type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007152", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007152", 
            "name": "arrhythmogenic right ventricular cardiomyopathy caused by mutation in TGFB3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007152", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007152", 
            "name": "cardiomyopathy, right ventricular dilated"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007152", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007152", 
            "name": "ARVD1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007152", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007152", 
            "name": "arrhythmogenic right ventricular dysplasia type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007152", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007152", 
            "name": "familial arrhythmogenic right ventricular dysplasia 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007152", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007152", 
            "name": "ARVC1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007152", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007152", 
            "name": "arrhythmogenic right ventricular dysplasia, familial, 1; ARVD1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007152", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007152", 
            "name": "arrhythmogenic right ventricular dysplasia, familial, 1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050431", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050431", 
            "name": "arrhythmogenic right ventricular dysplasia/cardiomyopathy"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050431", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050431", 
            "name": "ARVC"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050431", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050431", 
            "name": "ARVC cardiomyopathy"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050431", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050431", 
            "name": "ARVD"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050431", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050431", 
            "name": "arrhythmogenic right ventricular dysplasia"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050431", 
        "description": "An intrinsic cardiomyopathy that is characterized by hypokinetic areas involving the free wall of the right ventricle, with fibrofatty replacement of the right ventricular myocardium, with associated arrhythmias originating in the right ventricle.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050431", 
        "name": "arrhythmogenic right ventricular cardiomyopathy"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0050431#disease-associations", 
            "id": "0050431", 
            "database": "Alliance of Genome Resources"
        }
    ]
}