{
    "disease_id": "DOID:0111221",
    "recommended_name": {
        "id": "DOID:0111221",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111221",
        "name": "centronuclear myopathy 6 with fiber-type disproportion",
        "description": "An autosomal recessive centronuclear myopathy that is characterized by onset in infancy or early childhood of slowly progressive centronuclear myopathy that has_material_basis_in homozygous or compound heterozygous mutation in the ZAK gene on 2q31.1."
    },
    "synonyms": [
        {
            "id": "DOID:0111221",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111221",
            "name": "CNM6",
            "description": ""
        },
        {
            "id": "MONDO:0054695",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0054695",
            "name": "myopathy, centronuclear, 6, with fiber-type disproportion",
            "description": ""
        },
        {
            "id": "MONDO:0054695",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0054695",
            "name": "myopathy, centronuclear, 6, with fiber-type disproportion",
            "description": ""
        },
        {
            "id": "MONDO:0054695",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0054695",
            "name": "CNM6",
            "description": ""
        },
        {
            "id": "MIM:617760",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/617760",
            "name": "Myopathy, centronuclear, 6, with fiber-type disproportion",
            "description": "Myopathy, centronuclear, 6, with fiber-type disproportion"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111221"
    ],
    "unlinked_id_list": []
}