{
    "disease_id": "DOID:0110124", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014432", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014432", 
            "name": "Bardet-Biedl syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014432", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014432", 
            "name": "Bardet-Biedl syndrome 2; BBS2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014432", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014432", 
            "name": "Bardet-Biedl syndrome type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014432", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014432", 
            "name": "BBS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014432", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014432", 
            "name": "BBS2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014432", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014432", 
            "name": "BBS2 Bardet-Biedl syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014432", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014432", 
            "name": "Bardet-Biedl syndrome caused by mutation in BBS2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110124", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110124", 
            "name": "BBS2"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110124", 
        "description": "A Bardet-Biedl syndrome that has_material_basis_in homozygous or compound heterozygous mutations in the BBS2 gene on chromosome 16q13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110124", 
        "name": "Bardet-Biedl syndrome 2"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/615981", 
            "id": "615981", 
            "database": "MIM"
        }
    ]
}