{
    "disease_id": "DOID:0061251",
    "recommended_name": {
        "id": "DOID:0061251",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0061251",
        "name": "Charcot-Marie-Tooth disease type 2KK",
        "description": "A Charcot-Marie-Tooth disease type 2 characterized by motor nerves in the lower limbs, leading to gait difficulties with foot drop, increased falls, muscle atrophy of the lower limbs, and areflexia that has_material_basis_in homozygous mutation in the ARHGAP19 gene on chromosome 10q24."
    },
    "synonyms": [
        {
            "id": "MONDO:0980963",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0980963",
            "name": "Charcot-Marie-Tooth disease, axonal, type 2KK",
            "description": ""
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0061251"
    ],
    "unlinked_id_list": []
}