{
    "disease_id": "DOID:12930", 
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:12930", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:12930", 
            "name": "primary dilated cardiomyopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007269", 
            "description": "Familial dilated cardiomyopathy with conduction defect due to LMNA mutation is a rare familial dilated cardiomyopathy characterized by left ventricular enlargement and/or reduced systolic function preceded or accompanied by significant conduction system disease and/or arrhythmias including bradyarrhythmias, supraventricular or ventricular arrhythmias. Disease onset is usually in early to mid-adulthood. Sudden cardiac death may occur and may be the presenting symptom. In some cases, it is associated with skeletal myopathy and elevated serum creatine kinase.", 
            "resource": "MONDO", 
            "id": "MONDO:0007269", 
            "name": "dilated cardiomyopathy 1A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007269", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007269", 
            "name": "cardiomyopathy, idiopathic dilated"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007269", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007269", 
            "name": "LMNA familial isolated dilated cardiomyopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007269", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007269", 
            "name": "cardiomyopathy, dilated, with conduction defect 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007269", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007269", 
            "name": "familial dilated cardiomyopathy with conduction defect due to LMNA mutation"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007269", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007269", 
            "name": "cardiomyopathy, familial idiopathic"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007269", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007269", 
            "name": "CDCD1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007269", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007269", 
            "name": "dilated cardiomyopathy with conduction defect 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007269", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007269", 
            "name": "cardiomyopathy, dilated, 1A; CMD1A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007269", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007269", 
            "name": "cardiomyopathy, dilated, type 1A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007269", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007269", 
            "name": "cardiomyopathy, dilated, 1A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007269", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007269", 
            "name": "familial isolated dilated cardiomyopathy caused by mutation in LMNA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007269", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007269", 
            "name": "dilated cardiomyopathy type 1A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007269", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007269", 
            "name": "cardiomyopathy, congestive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007269", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007269", 
            "name": "CMD1A"
        }, 
        {
            "url": "https://www.omim.org/entry/115200", 
            "description": "Cardiomyopathy, dilated 1A", 
            "resource": "MIM", 
            "id": "MIM:115200", 
            "name": "Cardiomyopathy, dilated 1A"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:12930", 
        "description": "An intrinsic cardiomyopathy that is characterized by an an enlarged heart and damage to the myocardium causing the heart to pump blood inefficiently.", 
        "resource": "Disease Ontology", 
        "id": "DOID:12930", 
        "name": "dilated cardiomyopathy"
    }
}