{
    "disease_id": "DOID:0110167",
    "recommended_name": {
        "id": "DOID:0110167",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110167",
        "name": "Charcot-Marie-Tooth disease axonal type 2K",
        "description": "A Charcot-Marie-Tooth disease type 2 that has_material_basis_in homozygous or compound heterozygous mutation in the GDAP1 gene on chromosome 8q."
    },
    "synonyms": [
        {
            "id": "DOID:0110167",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110167",
            "name": "ARCMT2K",
            "description": ""
        },
        {
            "id": "DOID:0110167",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110167",
            "name": "Charcot-Marie-Tooth neuropathy axonal type 2K",
            "description": ""
        },
        {
            "id": "DOID:0110167",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110167",
            "name": "autosomal recessive axonal CMT4C4",
            "description": ""
        },
        {
            "id": "DOID:0110167",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110167",
            "name": "autosomal recessive Charcot-Marie-Tooth disease with hoarseness",
            "description": ""
        },
        {
            "id": "DOID:0110167",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110167",
            "name": "autosomal recessive axonal Charcot-Marie-Tooth disease disease type 2K",
            "description": ""
        },
        {
            "id": "DOID:0110167",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110167",
            "name": "autosomal recessive axonal Charcot-Marie-Tooth disease type 2K",
            "description": ""
        },
        {
            "id": "MONDO:0011916",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011916",
            "name": "Charcot-Marie-Tooth disease axonal type 2K",
            "description": "Autosomal recessive Charcot-Marie-Tooth disease with hoarseness (ARCMT2K or CMT4C4) is a severe early-onset form of axonal CMT peripheral sensorimotor polyneuropathy."
        },
        {
            "id": "MONDO:0011916",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011916",
            "name": "ARCMT2K",
            "description": ""
        },
        {
            "id": "MONDO:0011916",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011916",
            "name": "Charcot-Marie-Tooth disease, axonal, autosomal dominant, type 2K",
            "description": ""
        },
        {
            "id": "MONDO:0011916",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011916",
            "name": "autosomal recessive Charcot-Marie-Tooth disease with hoarseness",
            "description": ""
        },
        {
            "id": "MONDO:0011916",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011916",
            "name": "autosomal recessive axonal CMT4C4",
            "description": ""
        },
        {
            "id": "MONDO:0011916",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011916",
            "name": "autosomal recessive axonal Charcot-Marie-Tooth disease type 2K",
            "description": ""
        },
        {
            "id": "MONDO:0011916",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011916",
            "name": "CMT2K",
            "description": ""
        },
        {
            "id": "MONDO:0011916",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011916",
            "name": "Charcot-Marie-Tooth disease, axonal, type 2K",
            "description": ""
        },
        {
            "id": "MIM:607831",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/607831",
            "name": "Charcot-Marie-Tooth disease, axonal, type 2K",
            "description": "Charcot-Marie-Tooth disease, axonal, type 2K"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110167"
    ],
    "unlinked_id_list": []
}