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