{
    "disease_id": "DOID:0110429", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011425", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011425", 
            "name": "CMD1H"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011425", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011425", 
            "name": "cardiomyopathy, dilated, with conduction defect"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011425", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011425", 
            "name": "cardiomyopathy, dilated, 1H"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011425", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011425", 
            "name": "dilated cardiomyopathy type 1H"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011425", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011425", 
            "name": "cardiomyopathy, dilated, 1H; CMD1H"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011425", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011425", 
            "name": "dilated cardiomyopathy with conduction defect"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110429", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110429", 
            "name": "dilated cardiomyopathy with conduction defect"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110429", 
        "description": "A dilated cardiomyopathy that has_material_basis_in variation in the chromosome region 2q14-q22.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110429", 
        "name": "dilated cardiomyopathy 1H"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110429#disease-associations", 
            "id": "0110429", 
            "database": "Alliance of Genome Resources"
        }
    ]
}