{
    "disease_id": "DOID:0110160",
    "recommended_name": {
        "id": "DOID:0110160",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110160",
        "name": "Charcot-Marie-Tooth disease axonal type 2T",
        "description": "A Charcot-Marie-Tooth disease type 2 that has_material_basis_in homozygous or compound heterozygous mutation in the MME gene on chromosome 3q25."
    },
    "synonyms": [
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            "id": "DOID:0110160",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110160",
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        },
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            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110160",
            "name": "Charcot-Marie-Tooth neuropathy type 2T",
            "description": ""
        },
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            "url": "https://disease-ontology.org/term/DOID:0110160",
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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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            "description": ""
        },
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        }
    ],
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            "url": "https://disease-ontology.org/term/DOID:0110160",
            "categories": []
        },
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            "categories": []
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    "biomarkers": [],
    "association_flag": "1000",
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}