{
    "disease_id": "DOID:0110178",
    "recommended_name": {
        "id": "DOID:0110178",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110178",
        "name": "Charcot-Marie-Tooth disease axonal type 2V",
        "description": "A Charcot-Marie-Tooth disease type 2 that has_material_basis_in heterozygous mutation in the NAGLU gene on chromosome 17q21."
    },
    "synonyms": [
        {
            "id": "DOID:0110178",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110178",
            "name": "autosomal dominant Charcot-Marie-Tooth disease type 2V",
            "description": ""
        },
        {
            "id": "DOID:0110178",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110178",
            "name": "CMT2V",
            "description": ""
        },
        {
            "id": "DOID:0110178",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110178",
            "name": "Charcot-Marie-Tooth neuropathy type 2V",
            "description": ""
        },
        {
            "id": "DOID:0110178",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110178",
            "name": "autosomal dominant axonal Charcot-Marie-Tooth disease type 2V",
            "description": ""
        },
        {
            "id": "MONDO:0014665",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014665",
            "name": "Charcot-Marie-Tooth disease axonal type 2V",
            "description": "Any Charcot-Marie-Tooth disease in which the cause of the disease is a mutation in the NAGLU gene."
        },
        {
            "id": "MONDO:0014665",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014665",
            "name": "CMT2V",
            "description": ""
        },
        {
            "id": "MONDO:0014665",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014665",
            "name": "Charcot-Marie-Tooth disease caused by mutation in NAGLU",
            "description": ""
        },
        {
            "id": "MONDO:0014665",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014665",
            "name": "NAGLU Charcot-Marie-Tooth disease",
            "description": ""
        },
        {
            "id": "MONDO:0014665",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014665",
            "name": "autosomal dominant Charcot-Marie-Tooth disease type 2 due to NAGLU mutation",
            "description": ""
        },
        {
            "id": "MONDO:0014665",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014665",
            "name": "autosomal dominant Charcot-Marie-Tooth disease type 2V",
            "description": ""
        },
        {
            "id": "MONDO:0014665",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014665",
            "name": "hereditary adult-onset painful axonal polyneuropathy",
            "description": ""
        },
        {
            "id": "MONDO:0014665",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014665",
            "name": "Charcot-Marie-Tooth disease, axonal, type 2V",
            "description": ""
        },
        {
            "id": "MIM:616491",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/616491",
            "name": "Charcot-Marie-Tooth disease, axonal, type 2V",
            "description": "Charcot-Marie-Tooth disease, axonal, type 2V"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110178"
    ],
    "unlinked_id_list": []
}