{
    "disease_id": "DOID:0111223", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008048", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008048", 
            "name": "autosomal dominant centronuclear myopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008048", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008048", 
            "name": "DNM2-related centronuclear myopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008048", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008048", 
            "name": "CNM1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008048", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008048", 
            "name": "centronuclear myopathy, autosomal dominant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008048", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008048", 
            "name": "myopathy, centronuclear, 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008048", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008048", 
            "name": "myopathy, centronuclear, 1; CNM1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008048", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008048", 
            "name": "AD-CNM"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008048", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008048", 
            "name": "myopathy, centronuclear, autosomal dominant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008048", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008048", 
            "name": "myopathy, centronuclear, type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008048", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008048", 
            "name": "myotubular myopathy, autosomal dominant"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111223", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111223", 
            "name": "CNM1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111223", 
        "description": "An autosomal dominant centronuclear myopathy characterized by slowly progressive muscle wasting and weakness involving mainly the limb girdle, trunk, and neck muscles that has_material_basis_in heterozygous mutation in DNM2 on 19p13.2.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111223", 
        "name": "centronuclear myopathy 1"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111223#disease-associations", 
            "id": "0111223", 
            "database": "Alliance of Genome Resources"
        }
    ]
}