{
    "disease_id": "DOID:0111220", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009709", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009709", 
            "name": "myopathy, centronuclear, 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009709", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009709", 
            "name": "centronuclear myopathy caused by mutation in BIN1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009709", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009709", 
            "name": "BIN1 centronuclear myopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009709", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009709", 
            "name": "CNM2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009709", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009709", 
            "name": "myopathy, centronuclear, 2; CNM2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009709", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009709", 
            "name": "myopathy, centronuclear, type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009709", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009709", 
            "name": "myotubular myopathy, autosomal recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009709", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009709", 
            "name": "myopathy, centronuclear, autosomal recessive"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111220", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111220", 
            "name": "CNM2"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111220", 
        "description": "An autosomal recessive centronuclear myopathy that has_material_basis_in homozygous or compound heterozygous mutation in BIN1 on 2q14.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111220", 
        "name": "centronuclear myopathy 2"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111220#disease-associations", 
            "id": "0111220", 
            "database": "Alliance of Genome Resources"
        }
    ]
}