{
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    "synonyms": [
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            "description": "", 
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            "description": "", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010699", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010699", 
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            "description": "", 
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        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010699", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010699", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010699", 
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        }, 
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            "description": "", 
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            "id": "DOID:0110210", 
            "name": "Charcot-Marie-Tooth neuropathy X-linked recessive 5"
        }, 
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            "description": "", 
            "resource": "Disease Ontology", 
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        {
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            "description": "", 
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        }, 
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            "description": "", 
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            "description": "", 
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            "description": "", 
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        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110210", 
        "description": "A Charcot-Marie-Tooth disease X-linked that has_material_basis_in loss-of-function mutation in the PRPS1 gene on chromosome Xq22.", 
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    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110210#disease-associations", 
            "id": "0110210", 
            "database": "Alliance of Genome Resources"
        }
    ]
}