{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008854", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008854", 
            "name": "Bardet-Biedl syndrome 1; BBS1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008854", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008854", 
            "name": "Bardet-Biedl syndrome type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008854", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008854", 
            "name": "BBS1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110123", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110123", 
            "name": "BBS1"
        }, 
        {
            "url": "https://www.omim.org/entry/209900", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:209900", 
            "name": "Bardet-Biedl syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110123", 
        "description": "A Bardet-Biedl syndrome that has_material_basis_in homozygous mutation in the BBS1 gene on chromosome 11q13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110123", 
        "name": "Bardet-Biedl syndrome 1"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/209900", 
            "id": "209900", 
            "database": "MIM"
        }
    ]
}