{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013168", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013168", 
            "name": "familial isolated dilated cardiomyopathy caused by mutation in RBM20"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013168", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013168", 
            "name": "RBM20 familial isolated dilated cardiomyopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013168", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013168", 
            "name": "CMD1DD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013168", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013168", 
            "name": "cardiomyopathy, dilated, type 1Dd"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013168", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013168", 
            "name": "cardiomyopathy, dilated, 1DD; CMD1DD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013168", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013168", 
            "name": "cardiomyopathy, dilated, 1DD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013168", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013168", 
            "name": "dilated cardiomyopathy type 1DD"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110447", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110447", 
            "name": "CMD1DD"
        }, 
        {
            "url": "https://www.omim.org/entry/613172", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:613172", 
            "name": "Cardiomyopathy, dilated 1DD"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110447", 
        "description": "A dilated cardiomyopathy that has_material_basis_in mutation in the RBM20 gene on chromosome 10q25.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110447", 
        "name": "dilated cardiomyopathy 1DD"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/613172", 
            "id": "613172", 
            "database": "MIM"
        }
    ]
}