{
    "disease_id": "DOID:0111223",
    "recommended_name": {
        "id": "DOID:0111223",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111223",
        "name": "centronuclear myopathy 1",
        "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."
    },
    "synonyms": [
        {
            "id": "DOID:0111223",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111223",
            "name": "CNM1",
            "description": ""
        },
        {
            "id": "MONDO:0008048",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008048",
            "name": "autosomal dominant centronuclear myopathy",
            "description": "An inherited neuromuscular disorder defined by numerous centrally placed nuclei on muscle biopsy and clinical features of a congenital myopathy."
        },
        {
            "id": "MONDO:0008048",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008048",
            "name": "AD-CNM",
            "description": ""
        },
        {
            "id": "MONDO:0008048",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008048",
            "name": "CNM1",
            "description": ""
        },
        {
            "id": "MONDO:0008048",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008048",
            "name": "autosomal dominant centronuclear myopathy",
            "description": ""
        },
        {
            "id": "MONDO:0008048",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008048",
            "name": "autosomal dominant centronuclear myopathy caused by mutation in MYF6",
            "description": ""
        },
        {
            "id": "MONDO:0008048",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008048",
            "name": "centronuclear myopathy 1",
            "description": ""
        },
        {
            "id": "MONDO:0008048",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008048",
            "name": "centronuclear myopathy, autosomal dominant",
            "description": ""
        },
        {
            "id": "MONDO:0008048",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008048",
            "name": "centronuclear myopathy, autosomal, modifier of",
            "description": ""
        },
        {
            "id": "MONDO:0008048",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008048",
            "name": "myopathy, centronuclear, 1",
            "description": ""
        },
        {
            "id": "MONDO:0008048",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008048",
            "name": "myopathy, centronuclear, 3",
            "description": ""
        },
        {
            "id": "MONDO:0008048",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008048",
            "name": "myopathy, centronuclear, autosomal dominant",
            "description": ""
        },
        {
            "id": "MONDO:0008048",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008048",
            "name": "myopathy, centronuclear, type 1",
            "description": ""
        },
        {
            "id": "MONDO:0008048",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008048",
            "name": "myopathy, centronuclear, type 3",
            "description": ""
        },
        {
            "id": "MONDO:0008048",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008048",
            "name": "myotubular myopathy, autosomal dominant",
            "description": ""
        },
        {
            "id": "MONDO:0008048",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008048",
            "name": "CNM3",
            "description": ""
        },
        {
            "id": "MONDO:0008048",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008048",
            "name": "DNM2-related centronuclear myopathy",
            "description": ""
        },
        {
            "id": "MONDO:0008048",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008048",
            "name": "autosomal dominant centronuclear myopathy",
            "description": "An inherited neuromuscular disorder defined by numerous centrally placed nuclei on muscle biopsy and clinical features of a congenital myopathy."
        },
        {
            "id": "MONDO:0008048",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008048",
            "name": "AD-CNM",
            "description": ""
        },
        {
            "id": "MONDO:0008048",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008048",
            "name": "CNM1",
            "description": ""
        },
        {
            "id": "MONDO:0008048",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008048",
            "name": "autosomal dominant centronuclear myopathy",
            "description": ""
        },
        {
            "id": "MONDO:0008048",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008048",
            "name": "autosomal dominant centronuclear myopathy caused by mutation in MYF6",
            "description": ""
        },
        {
            "id": "MONDO:0008048",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008048",
            "name": "centronuclear myopathy 1",
            "description": ""
        },
        {
            "id": "MONDO:0008048",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008048",
            "name": "centronuclear myopathy, autosomal dominant",
            "description": ""
        },
        {
            "id": "MONDO:0008048",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008048",
            "name": "centronuclear myopathy, autosomal, modifier of",
            "description": ""
        },
        {
            "id": "MONDO:0008048",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008048",
            "name": "myopathy, centronuclear, 1",
            "description": ""
        },
        {
            "id": "MONDO:0008048",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008048",
            "name": "myopathy, centronuclear, 3",
            "description": ""
        },
        {
            "id": "MONDO:0008048",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008048",
            "name": "myopathy, centronuclear, autosomal dominant",
            "description": ""
        },
        {
            "id": "MONDO:0008048",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008048",
            "name": "myopathy, centronuclear, type 1",
            "description": ""
        },
        {
            "id": "MONDO:0008048",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008048",
            "name": "myopathy, centronuclear, type 3",
            "description": ""
        },
        {
            "id": "MONDO:0008048",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008048",
            "name": "myotubular myopathy, autosomal dominant",
            "description": ""
        },
        {
            "id": "MONDO:0008048",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008048",
            "name": "CNM3",
            "description": ""
        },
        {
            "id": "MONDO:0008048",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008048",
            "name": "DNM2-related centronuclear myopathy",
            "description": ""
        },
        {
            "id": "MIM:160150",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/160150",
            "name": "Myopathy, centronuclear, 1",
            "description": "Myopathy, centronuclear, 1"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111223"
    ],
    "unlinked_id_list": []
}