{
    "disease_id": "DOID:0110168",
    "recommended_name": {
        "id": "DOID:0110168",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110168",
        "name": "Charcot-Marie-Tooth disease type 2Y",
        "description": "A Charcot-Marie-Tooth disease type 2 that has_material_basis_in heterozygous mutation in the VCP gene on chromosome 9p13."
    },
    "synonyms": [
        {
            "id": "DOID:0110168",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110168",
            "name": "autosomal dominant axonal Charcot-Marie-Tooth type 2Y",
            "description": ""
        },
        {
            "id": "DOID:0110168",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110168",
            "name": "CMT2 due to VCP mutation",
            "description": ""
        },
        {
            "id": "DOID:0110168",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110168",
            "name": "CMT2Y",
            "description": ""
        },
        {
            "id": "DOID:0110168",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110168",
            "name": "Charcot-Marie-Tooth neuropathy type 2Y",
            "description": ""
        },
        {
            "id": "DOID:0110168",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110168",
            "name": "autosomal dominant Charcot-Marie-Tooth disease type 2 due to VCP mutation",
            "description": ""
        },
        {
            "id": "MONDO:0014735",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014735",
            "name": "Charcot-Marie-Tooth disease type 2Y",
            "description": "Any Charcot-Marie-Tooth disease type 2 in which the cause of the disease is a mutation in the VCP gene."
        },
        {
            "id": "MONDO:0014735",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014735",
            "name": "Charcot-Marie-Tooth disease, axonal, type 2y",
            "description": ""
        },
        {
            "id": "MONDO:0014735",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014735",
            "name": "Charcot-Marie-Tooth disease, axonal, type 2Y; CMT2Y",
            "description": ""
        },
        {
            "id": "MONDO:0014735",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014735",
            "name": "CMT2Y",
            "description": ""
        },
        {
            "id": "MONDO:0014735",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014735",
            "name": "autosomal dominant axonal Charcot-Marie-Tooth type 2Y",
            "description": ""
        },
        {
            "id": "MONDO:0014735",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014735",
            "name": "Charcot-Marie-Tooth neuropathy, type 2Y",
            "description": ""
        },
        {
            "id": "MONDO:0014735",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014735",
            "name": "autosomal dominant Charcot-Marie-Tooth disease type 2 due to VCP mutation",
            "description": ""
        },
        {
            "id": "MONDO:0014735",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014735",
            "name": "autosomal dominant Charcot-Marie-Tooth disease type 2Y",
            "description": ""
        },
        {
            "id": "MONDO:0014735",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014735",
            "name": "CMT2 due to VCP mutation",
            "description": ""
        },
        {
            "id": "MONDO:0014735",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014735",
            "name": "Charcot-Marie-Tooth disease, axonal, autosomal dominant, type 2Y",
            "description": ""
        },
        {
            "id": "MONDO:0014735",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014735",
            "name": "Charcot-Marie-Tooth disease type 2 caused by mutation in VCP",
            "description": ""
        },
        {
            "id": "MONDO:0014735",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014735",
            "name": "Charcot-Marie-Tooth neuropathy type 2Y",
            "description": ""
        },
        {
            "id": "MONDO:0014735",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014735",
            "name": "VCP Charcot-Marie-Tooth disease type 2",
            "description": ""
        },
        {
            "id": "MIM:616687",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/616687",
            "name": "Charcot-Marie-Tooth disease 2Y",
            "description": "Charcot-Marie-Tooth disease 2Y"
        }
    ]
}