{
    "disease_id": "DOID:0080068",
    "recommended_name": {
        "id": "DOID:0080068",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0080068",
        "name": "Charcot-Marie-Tooth disease type 6",
        "description": "A Charcot-Marie-Tooth disease that is characterized by early-onset optic atrophy resulting in progressive visual loss and peripheral axonal sensorimotor neuropathy with highly variable age at onset and severity."
    },
    "synonyms": [
        {
            "id": "DOID:0080068",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0080068",
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        },
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            "description": "Any hereditary motor and sensory neuropathy type 6 in which the cause of the disease is a mutation in the MFN2 gene."
        },
        {
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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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        },
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            "description": ""
        },
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            "resource": "MONDO",
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        },
        {
            "id": "MONDO:0014671",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014671",
            "name": "CMT6B",
            "description": ""
        },
        {
            "id": "MONDO:0014671",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014671",
            "name": "Charcot-Marie-Tooth disease, type 6B",
            "description": ""
        },
        {
            "id": "MONDO:0014671",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014671",
            "name": "HMSN 6B",
            "description": ""
        },
        {
            "id": "MONDO:0014671",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014671",
            "name": "HMSN6B",
            "description": ""
        },
        {
            "id": "MONDO:0014671",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014671",
            "name": "SLC25A46 hereditary motor and sensory neuropathy type 6",
            "description": ""
        },
        {
            "id": "MONDO:0014671",
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            "description": ""
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        },
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            "name": "neuropathy, hereditary motor and sensory, type VIB",
            "description": ""
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            "url": "https://www.omim.org/entry/601152",
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        }
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}