{
    "disease_id": "DOID:0110150", 
    "synonyms": [
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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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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011890", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011890", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011890", 
            "name": "HMSN 1D"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011890", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011890", 
            "name": "Charcot Marie Tooth disease type 1D"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011890", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011890", 
            "name": "CMT 1D"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011890", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011890", 
            "name": "Charcot-Marie-Tooth disease, demyelinating, type 1D; CMT1D"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011890", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011890", 
            "name": "CMT1D"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011890", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011890", 
            "name": "Charcot-Marie-Tooth disease type 1 caused by mutation in EGR2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011890", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011890", 
            "name": "HMSN ID"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110150", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110150", 
            "name": "CMT1D"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110150", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110150", 
            "name": "Charcot-Marie-Tooth neuropathy type 1D"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110150", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110150", 
            "name": "HMSN ID"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110150", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110150", 
            "name": "HMSN1D"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110150", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110150", 
            "name": "hereditary motor and sensory neuropathy 1D"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110150", 
        "description": "A Charcot-Marie-Tooth disease type 1 that has_material_basis_in mutation in the early growth response gene-2 (EGR2).", 
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        "id": "DOID:0110150", 
        "name": "Charcot-Marie-Tooth disease type 1D"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110150#disease-associations", 
            "id": "0110150", 
            "database": "Alliance of Genome Resources"
        }
    ]
}