{
    "disease_id": "DOID:0110163", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011687", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011687", 
            "name": "Charcot-Marie-Tooth disease, axonal, type 2F"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011687", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011687", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011687", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011687", 
            "name": "HSPB1 Charcot-Marie-Tooth disease type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011687", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011687", 
            "name": "Charcot-Marie-Tooth disease, neuronal, type 2F"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011687", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011687", 
            "name": "autosomal dominant Charcot-Marie-Tooth disease type 2F"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011687", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011687", 
            "name": "Charcot-Marie-Tooth disease type 2F"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011687", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011687", 
            "name": "Charcot-Marie-Tooth neuronal type 2F"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011687", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011687", 
            "name": "Charcot-Marie-Tooth neuropathy, type 2F"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011687", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011687", 
            "name": "CMT 2F"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011687", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011687", 
            "name": "Charcot-Marie-Tooth disease type 2 caused by mutation in HSPB1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011687", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011687", 
            "name": "Charcot Marie Tooth disease type 2F"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011687", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011687", 
            "name": "CMT2F"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011687", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011687", 
            "name": "Charcot-Marie-Tooth neuropathy type 2F"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110163", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110163", 
            "name": "CMT2F"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110163", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110163", 
            "name": "Charcot-Marie-Tooth neuronal type 2F"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110163", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110163", 
            "name": "Charcot-Marie-Tooth neuropathy type 2F"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110163", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110163", 
            "name": "autosomal dominant Charcot-Marie-Tooth disease type 2F"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110163", 
        "description": "A Charcot-Marie-Tooth  disease type 2 that has_material_basis_in mutation in the gene encoding heat-shock 27-kD protein-1 (HSPB1).", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110163", 
        "name": "Charcot-Marie-Tooth disease axonal type 2F"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110163#disease-associations", 
            "id": "0110163", 
            "database": "Alliance of Genome Resources"
        }
    ]
}