{
    "disease_id": "DOID:0081160",
    "recommended_name": {
        "id": "DOID:0081160",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0081160",
        "name": "dilated cardiomyopathy 2D",
        "description": "A dilated cardiomyopathy that is characterized by neonatal onset of severe cardiomyopathy, with rapid progression to cardiac decompensation and death unless the patient undergoes heart transplantation and that has_material_basis_in homozygous or compound heterozygous mutation in the RPL3L gene on chromosome 16p13."
    },
    "synonyms": [
        {
            "id": "MONDO:0030300",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030300",
            "name": "cardiomyopathy, dilated, 2D",
            "description": "A dilated cardiomyopathy that is characterized by neonatal onset of severe cardiomyopathy, with rapid progression to cardiac decompensation and death unless the patient undergoes heart transplantation and that has material basis in homozygous or compound heterozygous mutation in the RPL3L gene on chromosome 16p13."
        },
        {
            "id": "MONDO:0030300",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030300",
            "name": "CMD2D",
            "description": ""
        },
        {
            "id": "MONDO:0030300",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030300",
            "name": "cardiomyopathy, dilated, 2D",
            "description": ""
        },
        {
            "id": "MIM:619371",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/619371",
            "name": "Cardiomyopathy, dilated, 2D",
            "description": "Cardiomyopathy, dilated, 2D"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0081160"
    ],
    "unlinked_id_list": []
}