{
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:0110425", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110425", 
            "name": "familial dilated cardiomyopathy with conduction defect due to LMNA mutation"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110425", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110425", 
            "name": "CDCD1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110425", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110425", 
            "name": "dilated cardiomyopathy with conduction defect 1"
        }, 
        {
            "url": "https://www.omim.org/entry/115200", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:115200", 
            "name": "Cardiomyopathy, dilated 1A"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110425", 
        "description": "A dilated cardiomyopathy that has_material_basis_in mutation in the LMNA gene on chromosome 1q21.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110425", 
        "name": "dilated cardiomyopathy 1A"
    }
}