{
    "disease_id": "DOID:0111224", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013890", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013890", 
            "name": "congenital myopathy with internal nuclei and atypical cores"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013890", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013890", 
            "name": "myopathy, centronuclear, 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013890", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013890", 
            "name": "centronuclear myopathy type 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013890", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013890", 
            "name": "myopathy, centronuclear, 4; CNM4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013890", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013890", 
            "name": "CNM4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013890", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013890", 
            "name": "myopathy, centronuclear, type 4"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111224", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111224", 
            "name": "CNM4"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111224", 
        "description": "An autosomal dominant centronuclear myopathy that has_material_basis_in heterozygous mutation in CCDC78 on 16p13.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111224", 
        "name": "centronuclear myopathy 4"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111224#disease-associations", 
            "id": "0111224", 
            "database": "Alliance of Genome Resources"
        }
    ]
}