{
    "disease_id": "DOID:0110460", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012746", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012746", 
            "name": "cardiomyopathy, dilated, 2A; CMD2A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012746", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012746", 
            "name": "dilated cardiomyopathy type 2A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012746", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012746", 
            "name": "cardiomyopathy, dilated, type 2A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012746", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012746", 
            "name": "cardiomyopathy, dilated, autosomal recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012746", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012746", 
            "name": "CMD2A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012746", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012746", 
            "name": "cardiomyopathy, dilated, 2A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012746", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012746", 
            "name": "cardiomyopathy, congestive, autosomal recessive"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110460", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110460", 
            "name": "CMD2A"
        }, 
        {
            "url": "https://www.omim.org/entry/611880", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:611880", 
            "name": "Cardiomyopathy, dilated 2A"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110460", 
        "description": "A dilated cardiomyopathy that has_material_basis_in mutation in the TNNI3 gene on chromosome 19q13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110460", 
        "name": "dilated cardiomyopathy 2A"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/611880", 
            "id": "611880", 
            "database": "MIM"
        }
    ]
}