{
    "disease_id": "DOID:0110461",
    "recommended_name": {
        "id": "DOID:0110461",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110461",
        "name": "X-linked dilated cardiomyopathy",
        "description": "A dilated cardiomyopathy that has_material_basis_in mutation in the gene encoding dystrophin (DMD) on chromosome Xp21, without skeletal muscle weakness or wasting."
    },
    "synonyms": [
        {
            "id": "DOID:0110461",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110461",
            "name": "CMD3B",
            "description": ""
        },
        {
            "id": "DOID:0110461",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110461",
            "name": "DMD-related dilated cardiomyopathy",
            "description": ""
        }
    ]
}