{
    "disease_id": "DOID:0110180", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014836", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014836", 
            "name": "CMT2CC"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014836", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014836", 
            "name": "Charcot-Marie-Tooth disease, axonal, type 2CC; CMT2CC"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014836", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014836", 
            "name": "NEFH Charcot-Marie-Tooth disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014836", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014836", 
            "name": "Charcot-Marie-Tooth disease caused by mutation in NEFH"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014836", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014836", 
            "name": "Charcot-Marie-Tooth neuropathy type 2CC"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014836", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014836", 
            "name": "Charcot-Marie-Tooth neuropathy, type 2Cc"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014836", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014836", 
            "name": "Charcot-Marie-Tooth disease, axonal, type 2cc"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110180", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110180", 
            "name": "CMT2CC"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110180", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110180", 
            "name": "Charcot-Marie-Tooth neuropathy type 2CC"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110180", 
        "description": "A Charcot-Marie-Tooth disease type 2 that has_material_basis_in heterozygous mutation in the NEFH gene on chromosome 22q12.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110180", 
        "name": "Charcot-Marie-Tooth disease axonal type 2CC"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110180#disease-associations", 
            "id": "0110180", 
            "database": "Alliance of Genome Resources"
        }
    ]
}