{
    "disease_id": "DOID:0110187", 
    "synonyms": [
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            "description": "", 
            "resource": "MONDO", 
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            "description": "", 
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
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        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014733", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014733", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014733", 
            "name": "Charcot-Marie-Tooth neuropathy, demyelinating, autosomal recessive, type 4K"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110187", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110187", 
            "name": "CMT4K"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110187", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110187", 
            "name": "SURF1-related CMT4"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110187", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110187", 
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        }, 
        {
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            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110187", 
            "name": "SURF1-related severe demyelinating Charcot-Marie-Tooth disease"
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        {
            "url": "http://disease-ontology.org/term/DOID:0110187", 
            "description": "", 
            "resource": "Disease Ontology", 
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        }, 
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        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110187", 
        "description": "A Charcot-Marie-Tooth disease type 4 that has_material_basis_in homozygous or compound heterozygous mutation in the SURF1 gene on chromosome 9q34.", 
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        "id": "DOID:0110187", 
        "name": "Charcot-Marie-Tooth disease type 4K"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110187#disease-associations", 
            "id": "0110187", 
            "database": "Alliance of Genome Resources"
        }
    ]
}