{
    "disease_id": "DOID:0111559",
    "recommended_name": {
        "id": "DOID:0111559",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111559",
        "name": "Charcot-Marie-Tooth disease type 2EE",
        "description": "A Charcot-Marie-Tooth disease type 2 characterized by slowly progressive axonal neuropathy primarily affecting the lower limbs with onset in the first or second decades of life that has_material_basis_in homozygous or compound heterozygous mutation in MPV17 on chromosome 2p23.3."
    },
    "synonyms": [
        {
            "id": "DOID:0111559",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111559",
            "name": "CMT2EE",
            "description": ""
        },
        {
            "id": "DOID:0111559",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111559",
            "name": "Charcot-Marie-Tooth disease, axonal, type 2EE",
            "description": ""
        },
        {
            "id": "MIM:618400",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/618400",
            "name": "Charcot-Marie-Tooth disease, axonal, 2EE",
            "description": "Charcot-Marie-Tooth disease, axonal, 2EE"
        }
    ]
}