{
    "disease_id": "DOID:0111740", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010484", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010484", 
            "name": "deafness, X-linked 6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010484", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010484", 
            "name": "COL4A6 X-linked nonsyndromic deafness"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010484", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010484", 
            "name": "deafness, X-linked 6; DFNX6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010484", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010484", 
            "name": "X-linked nonsyndromic deafness caused by mutation in COL4A6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010484", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010484", 
            "name": "deafness, X-linked type 6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010484", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010484", 
            "name": "DFNX6"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111740", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111740", 
            "name": "DFNX6"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111740", 
        "description": "An X-linked nonsyndromic deafness characterized by severe bilateral sensorineural hearing loss with cochlear malformation in males and mild to moderate hearing loss in females with later onset that has_material_basis_in mutation in COL4A6 on chromosome Xq22.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111740", 
        "name": "X-linked deafness 6"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111740#disease-associations", 
            "id": "0111740", 
            "database": "Alliance of Genome Resources"
        }
    ]
}