{
    "disease_id": "DOID:0110203",
    "recommended_name": {
        "id": "DOID:0110203",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110203",
        "name": "Charcot-Marie-Tooth disease recessive intermediate D",
        "description": "A Charcot-Marie-Tooth disease intermediate type that has_material_basis_in homozygous mutation in the COX6A1 gene on chromosome 12q24."
    },
    "synonyms": [
        {
            "id": "DOID:0110203",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110203",
            "name": "CMTRID",
            "description": ""
        },
        {
            "id": "DOID:0110203",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110203",
            "name": "RI-CMT type D",
            "description": ""
        },
        {
            "id": "DOID:0110203",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110203",
            "name": "autosomal recessive intermediate Charcot-Marie-Tooth disease type D",
            "description": ""
        },
        {
            "id": "MONDO:0014467",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014467",
            "name": "Charcot-Marie-Tooth disease recessive intermediate D",
            "description": "Any Charcot-Marie-Tooth disease in which the cause of the disease is a mutation in the COX6A1 gene."
        },
        {
            "id": "MONDO:0014467",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014467",
            "name": "CMTRID",
            "description": ""
        },
        {
            "id": "MONDO:0014467",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014467",
            "name": "COX6A1 Charcot-Marie-Tooth disease",
            "description": ""
        },
        {
            "id": "MONDO:0014467",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014467",
            "name": "Charcot-Marie-Tooth disease caused by mutation in COX6A1",
            "description": ""
        },
        {
            "id": "MONDO:0014467",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014467",
            "name": "Charcot-Marie-Tooth disease recessive intermediate type D",
            "description": ""
        },
        {
            "id": "MONDO:0014467",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014467",
            "name": "Charcot-Marie-Tooth disease, recessive Intermediate type D",
            "description": ""
        },
        {
            "id": "MONDO:0014467",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014467",
            "name": "RI-CMT type D",
            "description": ""
        },
        {
            "id": "MONDO:0014467",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014467",
            "name": "autosomal recessive intermediate Charcot-Marie-Tooth disease type D",
            "description": ""
        },
        {
            "id": "MONDO:0014467",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014467",
            "name": "Charcot-Marie-Tooth disease, recessive intermediate D",
            "description": ""
        },
        {
            "id": "MIM:616039",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/616039",
            "name": "Charcot-Marie-Tooth disease, recessive intermediate D",
            "description": "Charcot-Marie-Tooth disease, recessive intermediate D"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110203"
    ],
    "unlinked_id_list": []
}