{
    "disease_id": "DOID:0110197", 
    "synonyms": [
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            "description": "", 
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            "description": "", 
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            "description": "", 
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            "description": "", 
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        {
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            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011674", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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            "name": "Charcot-Marie-Tooth disease dominant intermediate type B"
        }, 
        {
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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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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011674", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011674", 
            "name": "DNM2-related intermediate Charcot-Marie-Tooth neuropathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011674", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011674", 
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        }, 
        {
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        }, 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011674", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011674", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011674", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011674", 
            "name": "Charcot-Marie-Tooth disease caused by mutation in DNM2"
        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011674", 
            "name": "Charcot-Marie-Tooth neuropathy dominant intermediate B"
        }, 
        {
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            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110197", 
            "name": "CMTDI1"
        }, 
        {
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            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110197", 
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        }, 
        {
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            "description": "", 
            "resource": "Disease Ontology", 
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            "name": "DI-CMTB"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110197", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110197", 
            "name": "Charcot-Marie-Tooth neuropathy dominant intermediate B"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110197", 
        "description": "A Charcot-Marie-Tooth disease intermediate type that has_material_basis_in mutation in the gene encoding dynamin-2 (DNM2).", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110197", 
        "name": "Charcot-Marie-Tooth disease dominant intermediate B"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110197#disease-associations", 
            "id": "0110197", 
            "database": "Alliance of Genome Resources"
        }
    ]
}