{
    "disease_id": "DOID:0051043",
    "recommended_name": {
        "id": "DOID:0051043",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0051043",
        "name": "Charcot-Marie-Tooth disease axonal type 2JJ",
        "description": "A Charcot-Marie-Tooth disease type 2 that is characterized by adult onset of distal sensory impairment and distal muscle weakness and atrophy predominantly affecting the lower limbs and that has_material_basis_in heterozygous mutation in the BAG3 gene on chromosome 10q26."
    },
    "synonyms": [
        {
            "id": "DOID:0051043",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0051043",
            "name": "axonal Charcot-Marie-Tooth disease type 2JJ",
            "description": ""
        },
        {
            "id": "MONDO:0976227",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0976227",
            "name": "Charcot-Marie-tooth disease, axonal, type 2JJ",
            "description": ""
        },
        {
            "id": "MIM:621095",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/621095",
            "name": "Charcot-Marie-Tooth disease, axonal, type 2JJ",
            "description": "Charcot-Marie-Tooth disease, axonal, type 2JJ"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0051043"
    ],
    "unlinked_id_list": []
}