{
    "disease_id": "DOID:0111220",
    "recommended_name": {
        "id": "DOID:0111220",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111220",
        "name": "centronuclear myopathy 2",
        "description": "An autosomal recessive centronuclear myopathy that has_material_basis_in homozygous or compound heterozygous mutation in BIN1 on 2q14.3."
    },
    "synonyms": [
        {
            "id": "DOID:0111220",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111220",
            "name": "CNM2",
            "description": ""
        },
        {
            "id": "MONDO:0009709",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009709",
            "name": "myopathy, centronuclear, 2",
            "description": "Any centronuclear myopathy in which the cause of the disease is a mutation in the BIN1 gene."
        },
        {
            "id": "MONDO:0009709",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009709",
            "name": "centronuclear myopathy caused by mutation in BIN1",
            "description": ""
        },
        {
            "id": "MONDO:0009709",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009709",
            "name": "BIN1 centronuclear myopathy",
            "description": ""
        },
        {
            "id": "MONDO:0009709",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009709",
            "name": "CNM2",
            "description": ""
        },
        {
            "id": "MONDO:0009709",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009709",
            "name": "myopathy, centronuclear, 2; CNM2",
            "description": ""
        },
        {
            "id": "MONDO:0009709",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009709",
            "name": "myopathy, centronuclear, type 2",
            "description": ""
        },
        {
            "id": "MONDO:0009709",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009709",
            "name": "myopathy, centronuclear, 2",
            "description": ""
        },
        {
            "id": "MONDO:0009709",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009709",
            "name": "myotubular myopathy, autosomal recessive",
            "description": ""
        },
        {
            "id": "MONDO:0009709",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009709",
            "name": "myopathy, centronuclear, autosomal recessive",
            "description": ""
        },
        {
            "id": "MIM:255200",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/255200",
            "name": "Myopathy, centronuclear, 2",
            "description": "Myopathy, centronuclear, 2"
        }
    ]
}