{
    "disease_id": "DOID:0110127", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014434", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014434", 
            "name": "Bardet-Biedl syndrome 5; BBS5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014434", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014434", 
            "name": "BBS5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014434", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014434", 
            "name": "BBS5 Bardet-Biedl syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014434", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014434", 
            "name": "Bardet-Biedl syndrome type 5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014434", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014434", 
            "name": "Bardet-Biedl syndrome caused by mutation in BBS5"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110127", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110127", 
            "name": "BBS5"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110127", 
        "description": "A Bardet-Biedl syndrome that has_material_basis_in homozygous mutation in the BBS5 gene on chromosome 2q31.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110127", 
        "name": "Bardet-Biedl syndrome 5"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/615983", 
            "id": "615983", 
            "database": "MIM"
        }
    ]
}