{
    "disease_id": "DOID:0110175",
    "recommended_name": {
        "id": "DOID:0110175",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110175",
        "name": "Charcot-Marie-Tooth disease axonal type 2O",
        "description": "A Charcot-Marie-Tooth disease type 2 that has_material_basis_in heterozygous mutation in the DYNC1H1 gene on chromosome 14q32."
    },
    "synonyms": [
        {
            "id": "DOID:0110175",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110175",
            "name": "autosomal dominant axonal Charcot-Marie-Tooth disease type 2O",
            "description": ""
        },
        {
            "id": "DOID:0110175",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110175",
            "name": "Charcot-Marie-Tooth neuropathy axonal type 2O",
            "description": ""
        },
        {
            "id": "DOID:0110175",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110175",
            "name": "autosomal dominant Charcot-Marie-Tooth disease type 2O",
            "description": ""
        },
        {
            "id": "MONDO:0013644",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013644",
            "name": "Charcot-Marie-Tooth disease axonal type 2O",
            "description": "Any Charcot-Marie-Tooth disease in which the cause of the disease is a mutation in the DYNC1H1 gene."
        },
        {
            "id": "MONDO:0013644",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013644",
            "name": "Charcot-Marie-Tooth neuropathy, axonal, type 2O",
            "description": ""
        },
        {
            "id": "MONDO:0013644",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013644",
            "name": "Charcot-Marie-Tooth disease type 2O",
            "description": ""
        },
        {
            "id": "MONDO:0013644",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013644",
            "name": "CMT2O",
            "description": ""
        },
        {
            "id": "MONDO:0013644",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013644",
            "name": "Charcot-Marie-Tooth disease caused by mutation in DYNC1H1",
            "description": ""
        },
        {
            "id": "MONDO:0013644",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013644",
            "name": "autosomal dominant axonal Charcot-Marie-Tooth disease type 2O",
            "description": ""
        },
        {
            "id": "MONDO:0013644",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013644",
            "name": "Charcot-Marie-Tooth neuropathy axonal type 2O",
            "description": ""
        },
        {
            "id": "MONDO:0013644",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013644",
            "name": "Charcot-Marie-Tooth disease, axonal, type 2O; CMT2O",
            "description": ""
        },
        {
            "id": "MONDO:0013644",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013644",
            "name": "Charcot-Marie-Tooth disease, axonal, type 2O",
            "description": ""
        },
        {
            "id": "MONDO:0013644",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013644",
            "name": "Charcot-Marie-Tooth disease, axonal, autosomal dominant, type 2O",
            "description": ""
        },
        {
            "id": "MONDO:0013644",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013644",
            "name": "autosomal dominant Charcot-Marie-Tooth disease type 2O",
            "description": ""
        },
        {
            "id": "MONDO:0013644",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013644",
            "name": "DYNC1H1 Charcot-Marie-Tooth disease",
            "description": ""
        },
        {
            "id": "MIM:614228",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/614228",
            "name": "Charcot-Marie-Tooth disease 2O",
            "description": "Charcot-Marie-Tooth disease 2O"
        }
    ]
}