{
    "disease_id": "DOID:0111559", 
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:0111559", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111559", 
            "name": "CMT2EE"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111559", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111559", 
            "name": "Charcot-Marie-Tooth disease, axonal, type 2EE"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111559", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111559", 
        "name": "Charcot-Marie-Tooth disease type 2EE"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111559#disease-associations", 
            "id": "0111559", 
            "database": "Alliance of Genome Resources"
        }
    ]
}