{
    "disease_id": "DOID:0110425",
    "recommended_name": {
        "id": "DOID:0110425",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110425",
        "name": "dilated cardiomyopathy 1A",
        "description": "A dilated cardiomyopathy that has_material_basis_in mutation in the LMNA gene on chromosome 1q21."
    },
    "synonyms": [
        {
            "id": "DOID:0110425",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110425",
            "name": "familial dilated cardiomyopathy with conduction defect due to LMNA mutation",
            "description": ""
        },
        {
            "id": "DOID:0110425",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110425",
            "name": "CDCD1",
            "description": ""
        },
        {
            "id": "DOID:0110425",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110425",
            "name": "dilated cardiomyopathy with conduction defect 1",
            "description": ""
        },
        {
            "id": "MONDO:0007269",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007269",
            "name": "dilated cardiomyopathy 1A",
            "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."
        },
        {
            "id": "MONDO:0007269",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007269",
            "name": "CDCD1",
            "description": ""
        },
        {
            "id": "MONDO:0007269",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007269",
            "name": "LMNA familial isolated dilated cardiomyopathy",
            "description": ""
        },
        {
            "id": "MONDO:0007269",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007269",
            "name": "cardiomyopathy dilated with conduction defect type 1",
            "description": ""
        },
        {
            "id": "MONDO:0007269",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007269",
            "name": "cardiomyopathy, dilated, type 1A",
            "description": ""
        },
        {
            "id": "MONDO:0007269",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007269",
            "name": "dilated cardiomyopathy 1A",
            "description": ""
        },
        {
            "id": "MONDO:0007269",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007269",
            "name": "dilated cardiomyopathy type 1A",
            "description": ""
        },
        {
            "id": "MONDO:0007269",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007269",
            "name": "familial dilated cardiomyopathy with conduction defect due to LMNA mutation",
            "description": ""
        },
        {
            "id": "MONDO:0007269",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007269",
            "name": "familial isolated dilated cardiomyopathy caused by mutation in LMNA",
            "description": ""
        },
        {
            "id": "MONDO:0007269",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007269",
            "name": "cardiomyopathy, dilated, 1A",
            "description": ""
        },
        {
            "id": "MIM:115200",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/115200",
            "name": "Cardiomyopathy, dilated, 1A",
            "description": "Cardiomyopathy, dilated, 1A"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110425"
    ],
    "unlinked_id_list": []
}