{
    "disease_id": "DOID:0110345", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014544", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014544", 
            "name": "osteogenesis imperfecta, type XVI; OI16"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014544", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014544", 
            "name": "osteogenesis imperfecta type XVI"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014544", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014544", 
            "name": "chromosome 11P11.2 deletion syndrome, 91.3-Kb"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014544", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014544", 
            "name": "chromosome 11p11.2 deletion syndrome 91.3-KB"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014544", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014544", 
            "name": "osteogenesis imperfecta, type 16"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014544", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014544", 
            "name": "OI, type 16"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014544", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014544", 
            "name": "osteogenesis imperfecta, type XVI"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014544", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014544", 
            "name": "OI16"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110345", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110345", 
            "name": "OI16"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110345", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110345", 
            "name": "chromosome 11p11.2 deletion syndrome 91.3-KB"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110345", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110345", 
            "name": "osteogenesis imperfecta type XVI"
        }, 
        {
            "url": "https://www.omim.org/entry/616229", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:616229", 
            "name": "Osteogenesis imperfecta 16"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110345", 
        "description": "An osteogenesis imperfecta that has_material_basis_in contiguous gene deletion on chromosome 11p11.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110345", 
        "name": "osteogenesis imperfecta type 16"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/616229", 
            "id": "616229", 
            "database": "MIM"
        }
    ]
}
