{
    "disease_id": "DOID:0110445",
    "recommended_name": {
        "id": "DOID:0110445",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110445",
        "name": "dilated cardiomyopathy 1KK",
        "description": "A dilated cardiomyopathy that has_material_basis_in mutation in the MYPN gene on chromosome 10q21."
    },
    "synonyms": [
        {
            "id": "DOID:0110445",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110445",
            "name": "CMD1KK",
            "description": ""
        },
        {
            "id": "MONDO:0014100",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014100",
            "name": "dilated cardiomyopathy 1KK",
            "description": "Any dilated cardiomyopathy in which the cause of the disease is a mutation in the MYPN gene."
        },
        {
            "id": "MONDO:0014100",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014100",
            "name": "CMD1KK",
            "description": ""
        },
        {
            "id": "MONDO:0014100",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014100",
            "name": "MYPN dilated cardiomyopathy",
            "description": ""
        },
        {
            "id": "MONDO:0014100",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014100",
            "name": "cardiomyopathy, dilated, type 1Kk",
            "description": ""
        },
        {
            "id": "MONDO:0014100",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014100",
            "name": "cardiomyopathy, hypertrophic, 22",
            "description": ""
        },
        {
            "id": "MONDO:0014100",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014100",
            "name": "dilated cardiomyopathy caused by mutation in MYPN",
            "description": ""
        },
        {
            "id": "MONDO:0014100",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014100",
            "name": "dilated cardiomyopathy type 1KK",
            "description": ""
        },
        {
            "id": "MONDO:0014100",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014100",
            "name": "cardiomyopathy, dilated, 1KK",
            "description": ""
        },
        {
            "id": "MONDO:0014100",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014100",
            "name": "cardiomyopathy, familial hypertrophic, 22",
            "description": ""
        },
        {
            "id": "MONDO:0014100",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014100",
            "name": "cardiomyopathy, familial restrictive, 4",
            "description": ""
        },
        {
            "id": "MIM:615248",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/615248",
            "name": "Cardiomyopathy, dilated, 1KK",
            "description": "Cardiomyopathy, dilated, 1KK"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110445"
    ],
    "unlinked_id_list": []
}