{
    "disease_id": "DOID:0110316",
    "recommended_name": {
        "id": "DOID:0110316",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110316",
        "name": "hypertrophic cardiomyopathy 10",
        "description": "A familial hypertrophic cardiomyopathy that has_material_basis_in mutation in the MYL2 gene."
    },
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            "description": ""
        },
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        },
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        },
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            "description": ""
        },
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        },
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        },
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        },
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        },
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        },
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        },
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        }
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            "categories": []
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}