{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012586", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012586", 
            "name": "coronary artery disease, autosomal dominant 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012586", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012586", 
            "name": "coronary artery disease, autosomal dominant 2; ADCAD2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012586", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012586", 
            "name": "LRP6 coronary artery disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012586", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012586", 
            "name": "coronary artery disease, autosomal dominant type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012586", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012586", 
            "name": "ADCAD2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012586", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012586", 
            "name": "coronary artery disease caused by mutation in LRP6"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:3393", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:3393", 
            "name": "CHD"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:3393", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:3393", 
            "name": "Coronary disease"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:3393", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:3393", 
            "name": "coronary arteriosclerosis"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:3393", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:3393", 
            "name": "coronary heart disease"
        }, 
        {
            "url": "https://www.omim.org/entry/610947", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:610947", 
            "name": "Coronary artery disease, autosomal dominant, 2"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:3393", 
        "description": "An artery disease that is characterized by plaque building up along the inner walls of the arteries of the heart resulting in a narrowing of the arteries and a reduced blood supply to the cardiac muscles.", 
        "resource": "Disease Ontology", 
        "id": "DOID:3393", 
        "name": "coronary artery disease"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/610947", 
            "id": "610947", 
            "database": "MIM"
        }
    ]
}