{
    "disease_id": "DOID:0051028",
    "recommended_name": {
        "id": "DOID:0051028",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0051028",
        "name": "autosomal recessive axonal Charcot-Marie-Tooth disease with vocal cord paresis",
        "description": "A Charcot-Marie-Tooth disease type 4 that is characterized by the absence of sensory loss with an onset age of 15 to 25 years and that has_material_basis_in heterozygous mutation in the gene encoding heat-shock 22-kD protein-8 (HSPB8) on chromosome 12q24."
    },
    "synonyms": [
        {
            "id": "MONDO:0011898",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011898",
            "name": "Charcot-Marie-Tooth disease, axonal, with vocal cord paresis, autosomal recessive",
            "description": ""
        },
        {
            "id": "MONDO:0011898",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011898",
            "name": "Charcot-Marie-Tooth disease, axonal, with vocal cord paresis, autosomal recessive",
            "description": ""
        },
        {
            "id": "MIM:607706",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/607706",
            "name": "Charcot-Marie-Tooth disease, axonal, with vocal cord paresis, autosomal recessive",
            "description": "Charcot-Marie-Tooth disease, axonal, with vocal cord paresis, autosomal recessive"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0051028"
    ],
    "unlinked_id_list": []
}