{
    "disease_id": "DOID:0080294", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0036484", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0036484", 
            "name": "Charcot-Marie-Tooth disease, dominant intermediate G"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0036484", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0036484", 
            "name": "Charcot-Marie-Tooth disease dominant intermediate G"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0036484", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0036484", 
            "name": "Charcot-Marie-Tooth disease, dominant intermediate G; CMTDIG"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0036484", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0036484", 
            "name": "CMTDIG"
        }, 
        {
            "url": "https://www.omim.org/entry/617882", 
            "description": "Charcot-Marie-Tooth disease, dominant intermediate G", 
            "resource": "MIM", 
            "id": "MIM:617882", 
            "name": "Charcot-Marie-Tooth disease, dominant intermediate G"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080294", 
        "description": "A Charcot-Marie-Tooth disease intermediate type that has_material_basis_in heterozygous mutation in the NEFL gene on chromosome 8p21.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080294", 
        "name": "Charcot-Marie-Tooth disease dominant intermediate G"
    }
}