{
    "disease_id": "DOID:0110428",
    "recommended_name": {
        "id": "DOID:0110428",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110428",
        "name": "dilated cardiomyopathy 1AA",
        "description": "A dilated cardiomyopathy that has_material_basis_in mutation in the ACTN2 gene on chromosome 1q43."
    },
    "synonyms": [
        {
            "id": "DOID:0110428",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110428",
            "name": "dilated cardiomyopathy 1AA with or without left ventricular noncompaction",
            "description": ""
        },
        {
            "id": "DOID:0110428",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110428",
            "name": "CMD1AA",
            "description": ""
        },
        {
            "id": "MONDO:0012808",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012808",
            "name": "dilated cardiomyopathy 1AA",
            "description": "Any familial isolated dilated cardiomyopathy in which the cause of the disease is a mutation in the ACTN2 gene."
        },
        {
            "id": "MONDO:0012808",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012808",
            "name": "ACTN2 familial isolated dilated cardiomyopathy",
            "description": ""
        },
        {
            "id": "MONDO:0012808",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012808",
            "name": "CMD1AA",
            "description": ""
        },
        {
            "id": "MONDO:0012808",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012808",
            "name": "cardiomyopathy, dilated, 1AA, with or without LVNC",
            "description": ""
        },
        {
            "id": "MONDO:0012808",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012808",
            "name": "cardiomyopathy, hypertrophic, 23, with or without LVNC",
            "description": ""
        },
        {
            "id": "MONDO:0012808",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012808",
            "name": "dilated cardiomyopathy 1AA with or without left ventricular noncompaction",
            "description": ""
        },
        {
            "id": "MONDO:0012808",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012808",
            "name": "dilated cardiomyopathy type 1AA",
            "description": ""
        },
        {
            "id": "MONDO:0012808",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012808",
            "name": "familial isolated dilated cardiomyopathy caused by mutation in ACTN2",
            "description": ""
        },
        {
            "id": "MONDO:0012808",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012808",
            "name": "cardiomyopathy, dilated, 1AA, with or without left ventricular noncompaction",
            "description": ""
        },
        {
            "id": "MONDO:0012808",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012808",
            "name": "cardiomyopathy, familial hypertrophic, 23, with or without ventricular noncompaction",
            "description": ""
        },
        {
            "id": "MIM:612158",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/612158",
            "name": "Cardiomyopathy, dilated, 1AA, with or without left ventricular non-compaction",
            "description": "Cardiomyopathy, dilated, 1AA, with or without left ventricular non-compaction"
        }
    ]
}