{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014447", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014447", 
            "name": "Bardet-Biedl syndrome 19; BBS19"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014447", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014447", 
            "name": "Bardet-Biedl syndrome type 19"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014447", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014447", 
            "name": "Bardet-Biedl syndrome caused by mutation in IFT27"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014447", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014447", 
            "name": "BBS19"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014447", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014447", 
            "name": "IFT27 Bardet-Biedl syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110141", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110141", 
            "name": "BBS19"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110141", 
        "description": "A Bardet-Biedl syndrome that has_material_basis_in homozygous mutation in the IFT27 gene on chromosome 22q12.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110141", 
        "name": "Bardet-Biedl syndrome 19"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/615996", 
            "id": "615996", 
            "database": "MIM"
        }
    ]
}