{
    "disease_id": "DOID:0111558",
    "recommended_name": {
        "id": "DOID:0111558",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111558",
        "name": "Charcot-Marie-Tooth disease type 2DD",
        "description": "A Charcot-Marie-Tooth disease type 2 characterized by neuropathy mainly affecting the lower limbs that has_material_basis_in heterozygous mutation in the ATP1A1 gene on chromosome 1p13.1."
    },
    "synonyms": [
        {
            "id": "DOID:0111558",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111558",
            "name": "ATP1A1-related autosomal dominant Charcot-Marie-Tooth disease type 2",
            "description": ""
        },
        {
            "id": "DOID:0111558",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111558",
            "name": "ATP1A1-related CMT2",
            "description": ""
        },
        {
            "id": "DOID:0111558",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111558",
            "name": "CMT2DD",
            "description": ""
        },
        {
            "id": "DOID:0111558",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111558",
            "name": "Charcot-Marie-Tooth disease, axonal, type 2DD",
            "description": ""
        },
        {
            "id": "DOID:0111558",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111558",
            "name": "Charcot-Marie-Tooth neuropathy, type 2DD",
            "description": ""
        },
        {
            "id": "MONDO:0054833",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0054833",
            "name": "Charcot-Marie-tooth disease, axonal, type 2DD",
            "description": ""
        },
        {
            "id": "MONDO:0054833",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0054833",
            "name": "CMT2DD",
            "description": ""
        },
        {
            "id": "MIM:618036",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/618036",
            "name": "Charcot-Marie-Tooth disease, axonal, type 2DD",
            "description": "Charcot-Marie-Tooth disease, axonal, type 2DD"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111558"
    ],
    "unlinked_id_list": []
}