{
    "disease_id": "DOID:0080097",
    "recommended_name": {
        "id": "DOID:0080097",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0080097",
        "name": "myofibrillar myopathy 6",
        "description": "A myofibrillar myopathy 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": "BAG3-related myofibrillar myopathy",
            "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": "muscular dystrophy, Selcen type",
            "description": ""
        },
        {
            "id": "MONDO:0013061",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013061",
            "name": "myopathy, myofibrillar, 6",
            "description": ""
        },
        {
            "id": "MONDO:0013061",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013061",
            "name": "myopathy, myofibrillar, Bag3-related",
            "description": ""
        },
        {
            "id": "MIM:612954",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/612954",
            "name": "Myopathy, myofibrillar, 6",
            "description": "Myopathy, myofibrillar, 6"
        }
    ]
}