{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012025", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012025", 
            "name": "branchiootic syndrome 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012025", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012025", 
            "name": "branchiootic syndrome 3; BOS3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012025", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012025", 
            "name": "branchiootic syndrome caused by mutation in SIX1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012025", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012025", 
            "name": "branchiootic syndrome type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012025", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012025", 
            "name": "BOS3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012025", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012025", 
            "name": "bo syndrome 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012025", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012025", 
            "name": "SIX1 branchiootic syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060232", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060232", 
            "name": "BO syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060232", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060232", 
            "name": "BOR"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060232", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060232", 
            "name": "branchiootic dysplasia"
        }, 
        {
            "url": "https://www.omim.org/entry/608389", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:608389", 
            "name": "Branchiootic syndrome 3"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060232", 
        "description": "A syndrome characterized by malformations of the outer, middle and inner ear and branchial and renal malformations. Mutations of the EYA1, SIX1 and SIX5 genes are associated with the syndrome.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060232", 
        "name": "branchiootic syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/608389", 
            "id": "608389", 
            "database": "MIM"
        }
    ]
}