{
    "disease_id": "DOID:0110162",
    "recommended_name": {
        "id": "DOID:0110162",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110162",
        "name": "Charcot-Marie-Tooth disease, axonal type 2W",
        "description": "A Charcot-Marie-Tooth disease type 2 that has_material_basis_in heterozygous mutation in the HARS gene on chromosome 5q31."
    },
    "synonyms": [
        {
            "id": "DOID:0110162",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110162",
            "name": "CMT2W",
            "description": ""
        },
        {
            "id": "DOID:0110162",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110162",
            "name": "Charcot-Marie-Tooth neuropathy type 2W",
            "description": ""
        },
        {
            "id": "DOID:0110162",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110162",
            "name": "autosomal dominant axonal Charcot-Marie-Tooth disease type 2W",
            "description": ""
        },
        {
            "id": "MONDO:0014711",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014711",
            "name": "autosomal dominant Charcot-Marie-Tooth disease type 2W",
            "description": "Any Charcot-Marie-Tooth disease type 2 in which the cause of the disease is a mutation in the HARS gene."
        },
        {
            "id": "MONDO:0014711",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014711",
            "name": "CMT2W",
            "description": ""
        },
        {
            "id": "MONDO:0014711",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014711",
            "name": "Charcot-Marie-Tooth disease type 2 caused by mutation in HARS",
            "description": ""
        },
        {
            "id": "MONDO:0014711",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014711",
            "name": "Charcot-Marie-Tooth disease, axonal, type 2w",
            "description": ""
        },
        {
            "id": "MONDO:0014711",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014711",
            "name": "HARS Charcot-Marie-Tooth disease type 2",
            "description": ""
        },
        {
            "id": "MONDO:0014711",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014711",
            "name": "autosomal dominant Charcot-Marie-Tooth disease type 2 due to HARS mutation",
            "description": ""
        },
        {
            "id": "MIM:616625",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/616625",
            "name": "Charcot-Marie-Tooth disease, axonal, type 2W",
            "description": "Charcot-Marie-Tooth disease, axonal, type 2W"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110162"
    ],
    "unlinked_id_list": []
}