{
    "disease_id": "DOID:0110167",
    "recommended_name": {
        "id": "DOID:0110167",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110167",
        "name": "Charcot-Marie-Tooth disease axonal type 2K",
        "description": "A Charcot-Marie-Tooth disease type 2 that has_material_basis_in homozygous or compound heterozygous mutation in the GDAP1 gene on chromosome 8q."
    },
    "synonyms": [
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            "description": ""
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            "description": ""
        },
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            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110167",
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            "description": ""
        },
        {
            "id": "DOID:0110167",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110167",
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            "description": ""
        },
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            "url": "https://disease-ontology.org/term/DOID:0110167",
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            "description": ""
        },
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        },
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            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011916",
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            "description": ""
        },
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            "url": "https://monarchinitiative.org/disease/MONDO:0011916",
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        },
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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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    "glycans": [],
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    "association_flag": "1000",
    "record_id": "doid.0110167"
}