{
    "disease_id": "DOID:0080097",
    "recommended_name": {
        "id": "DOID:0080097",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0080097",
        "name": "myofibrillar myopathy 6",
        "description": "A myofibrillar myopathy that is characterized by onset in the first decade of progressive generalized and proximal muscle weakness, respiratory insufficiency, cardiomyopathy, and skeletal deformities related to muscle weakness and that has_material_basis_in heterozygous mutation in the BAG3 gene on chromosome 10q26."
    },
    "synonyms": [
        {
            "id": "MONDO:0013061",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013061",
            "name": "myofibrillar myopathy 6",
            "description": "Selcen type muscular dystrophy is characterized by progressive limb and axial muscle weakness associated with cardiomyopathy and severe respiratory insufficiency during adolescence. The disease manifests during childhood and progresses rapidly."
        },
        {
            "id": "MONDO:0013061",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013061",
            "name": "BAG3 myofibrillar myopathy (disease)",
            "description": ""
        },
        {
            "id": "MONDO:0013061",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013061",
            "name": "myofibrillar myopathy (disease) caused by mutation in BAG3",
            "description": ""
        },
        {
            "id": "MONDO:0013061",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013061",
            "name": "myofibrillar myopathy 6",
            "description": ""
        },
        {
            "id": "MONDO:0013061",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013061",
            "name": "myofibrillar myopathy type 6",
            "description": ""
        },
        {
            "id": "MONDO:0013061",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013061",
            "name": "myopathy, myofibrillar, type 6",
            "description": ""
        },
        {
            "id": "MONDO:0013061",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013061",
            "name": "MFM6",
            "description": ""
        },
        {
            "id": "MONDO:0013061",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013061",
            "name": "myopathy, myofibrillar, 6",
            "description": ""
        },
        {
            "id": "MIM:612954",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/612954",
            "name": "Myopathy, myofibrillar, 6",
            "description": "Myopathy, myofibrillar, 6"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0080097"
    ],
    "unlinked_id_list": []
}