{
    "disease_id": "DOID:0110149",
    "recommended_name": {
        "id": "DOID:0110149",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110149",
        "name": "Charcot-Marie-Tooth disease type 1F",
        "description": "A Charcot-Marie-Tooth disease type 1 that has_material_basis_in mutation in the NEFL gene."
    },
    "synonyms": [
        {
            "id": "DOID:0110149",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110149",
            "name": "CMT1F",
            "description": ""
        },
        {
            "id": "DOID:0110149",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110149",
            "name": "Charcot-Marie-Tooth neuropathy type 1F",
            "description": ""
        },
        {
            "id": "MONDO:0011902",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011902",
            "name": "Charcot-Marie-Tooth disease type 1F",
            "description": "gene (8p21.2)."
        },
        {
            "id": "MONDO:0011902",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011902",
            "name": "Charcot-Marie-Tooth neuropathy type 1F",
            "description": ""
        },
        {
            "id": "MONDO:0011902",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011902",
            "name": "Charcot-Marie-Tooth disease, demyelinating, type 1F; CMT1F",
            "description": ""
        },
        {
            "id": "MONDO:0011902",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011902",
            "name": "Charcot Marie Tooth disease type 1F",
            "description": ""
        },
        {
            "id": "MONDO:0011902",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011902",
            "name": "CMT 1F",
            "description": ""
        },
        {
            "id": "MONDO:0011902",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011902",
            "name": "NEFL Charcot-Marie-Tooth disease type 1",
            "description": ""
        },
        {
            "id": "MONDO:0011902",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011902",
            "name": "CMT1F",
            "description": ""
        },
        {
            "id": "MONDO:0011902",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011902",
            "name": "Charcot-Marie-Tooth neuropathy, type 1F",
            "description": ""
        },
        {
            "id": "MONDO:0011902",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011902",
            "name": "Charcot-Marie-Tooth disease type 1 caused by mutation in NEFL",
            "description": ""
        },
        {
            "id": "MONDO:0011902",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011902",
            "name": "Charcot-Marie-Tooth disease, demyelinating, type 1F",
            "description": ""
        },
        {
            "id": "MIM:607734",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/607734",
            "name": "Charcot-Marie-Tooth disease 1F",
            "description": "Charcot-Marie-Tooth disease 1F"
        }
    ]
}