{
    "disease_id": "DOID:14702", 
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:14702", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:14702", 
            "name": "Branchio-Oto-renal syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:14702", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:14702", 
            "name": "Branchio-otorenal dysplasia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:14702", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:14702", 
            "name": "Melnick-Fraser syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:14702", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:14702", 
            "name": "branchiootorenal dysplasia"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:14702", 
        "description": "A syndrome characterized by branchial arch anomalies (branchial fistulas, clefts, or cysts), hearing impairment, structural defects of the outer, middle, and inner ear, and renal abnormalities.", 
        "resource": "Disease Ontology", 
        "id": "DOID:14702", 
        "name": "branchiootorenal syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/14702#disease-associations", 
            "id": "14702", 
            "database": "Alliance of Genome Resources"
        }
    ]
}