{
    "disease_id": "DOID:0110444",
    "recommended_name": {
        "id": "DOID:0110444",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110444",
        "name": "dilated cardiomyopathy 1X",
        "description": "A dilated cardiomyopathy that has_material_basis_in mutation in the FKTN gene on chromosome 9q31."
    },
    "synonyms": [
        {
            "id": "DOID:0110444",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110444",
            "name": "dilated cardiomyopathy with mild or no proximal muscle weakness",
            "description": ""
        },
        {
            "id": "DOID:0110444",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110444",
            "name": "CMD1X",
            "description": ""
        },
        {
            "id": "MONDO:0012704",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012704",
            "name": "dilated cardiomyopathy 1X",
            "description": "Any familial isolated dilated cardiomyopathy in which the cause of the disease is a mutation in the FKTN gene."
        },
        {
            "id": "MONDO:0012704",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012704",
            "name": "CMD1X",
            "description": ""
        },
        {
            "id": "MONDO:0012704",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012704",
            "name": "FKTN familial isolated dilated cardiomyopathy",
            "description": ""
        },
        {
            "id": "MONDO:0012704",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012704",
            "name": "cardiomyopathy, dilated, type 1X",
            "description": ""
        },
        {
            "id": "MONDO:0012704",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012704",
            "name": "dilated cardiomyopathy type 1X",
            "description": ""
        },
        {
            "id": "MONDO:0012704",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012704",
            "name": "familial isolated dilated cardiomyopathy caused by mutation in FKTN",
            "description": ""
        },
        {
            "id": "MONDO:0012704",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012704",
            "name": "cardiomyopathy, dilated, 1X",
            "description": ""
        },
        {
            "id": "MIM:611615",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/611615",
            "name": "Cardiomyopathy, dilated, 1X",
            "description": "Cardiomyopathy, dilated, 1X"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110444"
    ],
    "unlinked_id_list": []
}