{
    "disease_id": "DOID:0110351",
    "recommended_name": {
        "id": "DOID:0110351",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110351",
        "name": "osteogenesis imperfecta type 11",
        "description": "An osteogenesis imperfecta that has_material_basis_in mutation in the FKBP10 gene on chromosome 17q21."
    },
    "synonyms": [
        {
            "id": "DOID:0110351",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110351",
            "name": "OI11",
            "description": ""
        },
        {
            "id": "DOID:0110351",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110351",
            "name": "osteogenesis imperfecta type XI",
            "description": ""
        },
        {
            "id": "MONDO:0012592",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012592",
            "name": "osteogenesis imperfecta type 11",
            "description": "Any osteogenesis imperfecta in which the cause of the disease is a mutation in the FKBP10 gene."
        },
        {
            "id": "MONDO:0012592",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012592",
            "name": "OI11",
            "description": ""
        },
        {
            "id": "MONDO:0012592",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012592",
            "name": "FKBP10 osteogenesis imperfecta",
            "description": ""
        },
        {
            "id": "MONDO:0012592",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012592",
            "name": "osteogenesis imperfecta type XI",
            "description": ""
        },
        {
            "id": "MONDO:0012592",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012592",
            "name": "osteogenesis imperfecta, type 11",
            "description": ""
        },
        {
            "id": "MONDO:0012592",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012592",
            "name": "OI type XI",
            "description": ""
        },
        {
            "id": "MONDO:0012592",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012592",
            "name": "OI, type 11",
            "description": ""
        },
        {
            "id": "MONDO:0012592",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012592",
            "name": "osteogenesis imperfecta, type XI; OI11",
            "description": ""
        },
        {
            "id": "MONDO:0012592",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012592",
            "name": "OI type 11",
            "description": ""
        },
        {
            "id": "MONDO:0012592",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012592",
            "name": "osteogenesis imperfecta, type XI",
            "description": ""
        },
        {
            "id": "MONDO:0012592",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012592",
            "name": "osteogenesis imperfecta caused by mutation in FKBP10",
            "description": ""
        },
        {
            "id": "MIM:610968",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/610968",
            "name": "Osteogenesis imperfecta 11",
            "description": "Osteogenesis imperfecta 11"
        }
    ]
}