{
    "disease_id": "DOID:0060231", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012217", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012217", 
            "name": "Bruck syndrome 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012217", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012217", 
            "name": "Bruck syndrome caused by mutation in PLOD2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012217", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012217", 
            "name": "BRKS2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012217", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012217", 
            "name": "Bruck syndrome type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012217", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012217", 
            "name": "Bruck syndrome 2; BRKS2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012217", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012217", 
            "name": "osteogenesis imperfecta with congenital Joint contractures"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012217", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012217", 
            "name": "PLOD2 Bruck syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060231", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060231", 
            "name": "osteogenesis imperfecta with congenital joint contractures"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060231", 
        "description": "A syndrome characterized by a combination of multiple joint contractures and osteogenesis imperfecta.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060231", 
        "name": "Bruck syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060231#disease-associations", 
            "id": "0060231", 
            "database": "Alliance of Genome Resources"
        }
    ]
}