{
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    "synonyms": [
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            "description": "", 
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            "description": "", 
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            "resource": "MONDO", 
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            "description": "", 
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            "description": "", 
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010949", 
            "name": "peripheral sensory neuropathy, autosomal dominant (PSN)"
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            "description": "", 
            "resource": "MONDO", 
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            "description": "", 
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        {
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            "description": "", 
            "resource": "MONDO", 
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            "url": "https://monarchinitiative.org/disease/MONDO:0010949", 
            "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": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110159", 
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        }, 
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            "description": "", 
            "resource": "Disease Ontology", 
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            "description": "", 
            "resource": "Disease Ontology", 
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            "name": "Charcot-Marie-Tooth neuropathy type 2B"
        }, 
        {
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            "description": "", 
            "resource": "Disease Ontology", 
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            "description": "", 
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        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110159", 
        "description": "A Charcot-Marie-Tooth disease type 2 that has_material_basis_in heterozygous mutation in the RAB7 gene on chromosome 3q21.", 
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        "name": "Charcot-Marie-Tooth disease type 2B"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110159#disease-associations", 
            "id": "0110159", 
            "database": "Alliance of Genome Resources"
        }
    ]
}