{
    "disease_id": "DOID:0111221", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0054695", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0054695", 
            "name": "myopathy, centronuclear, 6, with fiber-type disproportion"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0054695", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0054695", 
            "name": "myopathy, centronuclear, 6, with FIBER-type disproportion; CNM6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0054695", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0054695", 
            "name": "CNM6"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111221", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111221", 
            "name": "CNM6"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111221", 
        "description": "A congenital fiber-type disproportion characterized by onset in infancy or early childhood of slowly progressive centronuclear myopathy that has_material_basis_in homozygous or compound heterozygous mutation in ZAK on 2q31.1.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111221", 
        "name": "centronuclear myopathy 6 with fiber-type disproportion"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111221#disease-associations", 
            "id": "0111221", 
            "database": "Alliance of Genome Resources"
        }
    ]
}