{
    "disease_id": "DOID:0111269",
    "recommended_name": {
        "id": "DOID:0111269",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111269",
        "name": "autosomal dominant hyaline body myopathy",
        "description": "A hyaline body myopathy that has_material_basis_in heterozygous mutation in MYH7 on 14q11.2."
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            "name": "MSMA",
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            "name": "Myopathy, myosin storage, autosomal dominant",
            "description": ""
        },
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            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111269",
            "name": "myopathy with lysis of type I myofibrils",
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            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111269",
            "name": "congenital myopathy 7A",
            "description": ""
        },
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            "url": "https://disease-ontology.org/term/DOID:0111269",
            "name": "autosomal dominant myosin storage congenital myopathy 7A",
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            "name": "MSMA",
            "description": ""
        },
        {
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            "url": "https://monarchinitiative.org/disease/MONDO:0008409",
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            "description": ""
        },
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        },
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        },
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        },
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            "description": ""
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            "description": ""
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            "description": ""
        },
        {
            "id": "MIM:608358",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/608358",
            "name": "Congenital myopathy 7A, myosin storage, autosomal dominant",
            "description": "Congenital myopathy 7A, myosin storage, autosomal dominant"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111269"
    ],
    "unlinked_id_list": []
}