{
    "disease_id": "DOID:0111738", 
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:0111738", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111738", 
            "name": "X-linked external auditory canal atresia-dilated internal auditory canal-facial dysmorphism syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111738", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111738", 
            "name": "DFNX7"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111738", 
        "description": "An X-linked nonsyndromic deafness characterized by congenital, bilateral, mixed or conductive hearing loss and other ear anomalies that has_material_basis_in homozygous or hemizygous mutation in GPRASP2 on chromosome Xq22.1.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111738", 
        "name": "X-linked deafness 7"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111738#disease-associations", 
            "id": "0111738", 
            "database": "Alliance of Genome Resources"
        }
    ]
}