{
    "disease_id": "DOID:0110193", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013959", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013959", 
            "name": "Charcot-Marie-Tooth disease, demyelinating, type 4F"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013959", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013959", 
            "name": "Charcot-Marie-Tooth disease, demyelinating, type 4F; CMT4F"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013959", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013959", 
            "name": "Charcot-Marie-Tooth disease type 4 caused by mutation in Prx"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013959", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013959", 
            "name": "PRX Charcot-Marie-Tooth disease type 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013959", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013959", 
            "name": "CMT4F"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110193", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110193", 
            "name": "CMT4F"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110193", 
        "description": "A Charcot-Marie-Tooth disease type 4 that has_material_basis_in homozygous or compound heterozygous mutation in the periaxin gene (PRX) on chromosome 19q13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110193", 
        "name": "Charcot-Marie-Tooth disease type 4F"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110193#disease-associations", 
            "id": "0110193", 
            "database": "Alliance of Genome Resources"
        }
    ]
}