{
    "disease_id": "DOID:0110338",
    "recommended_name": {
        "id": "DOID:0110338",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110338",
        "name": "osteogenesis imperfecta type 17",
        "description": "An osteogenesis imperfecta that has_material_basis_in mutation in the SPARC gene on chromosome 5q33."
    },
    "synonyms": [
        {
            "id": "DOID:0110338",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110338",
            "name": "OI17",
            "description": ""
        },
        {
            "id": "DOID:0110338",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110338",
            "name": "osteogenesis imperfecta type XVII",
            "description": ""
        },
        {
            "id": "MONDO:0014672",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014672",
            "name": "osteogenesis imperfecta type 17",
            "description": "Any osteogenesis imperfecta in which the cause of the disease is a mutation in the SPARC gene."
        },
        {
            "id": "MONDO:0014672",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014672",
            "name": "osteogenesis imperfecta type XVII",
            "description": ""
        },
        {
            "id": "MONDO:0014672",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014672",
            "name": "SPARC osteogenesis imperfecta",
            "description": ""
        },
        {
            "id": "MONDO:0014672",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014672",
            "name": "OI17",
            "description": ""
        },
        {
            "id": "MONDO:0014672",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014672",
            "name": "osteogenesis imperfecta caused by mutation in SPARC",
            "description": ""
        },
        {
            "id": "MONDO:0014672",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014672",
            "name": "osteogenesis imperfecta, type XVII",
            "description": ""
        },
        {
            "id": "MONDO:0014672",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014672",
            "name": "osteogenesis imperfecta, type 17",
            "description": ""
        },
        {
            "id": "MONDO:0008148",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008148",
            "name": "osteogenesis imperfecta type 4",
            "description": "Osteogenesis imperfecta type IV is a moderate type of osteogenesis imperfecta (OI), a genetic disorder characterized by increased bone fragility, low bone mass and susceptibility to bone fractures. Patients with type IV have moderately short stature, mild to moderate scoliosis, grayish or white sclera, and dentinogenesis imperfecta (DI)."
        },
        {
            "id": "MONDO:0008148",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008148",
            "name": "common variable OI with normal sclerae",
            "description": ""
        },
        {
            "id": "MONDO:0008148",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008148",
            "name": "osteogenesis imperfecta with normal sclera",
            "description": ""
        },
        {
            "id": "MONDO:0008148",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008148",
            "name": "osteogenesis imperfecta type IV",
            "description": ""
        },
        {
            "id": "MONDO:0008148",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008148",
            "name": "OI type 4",
            "description": ""
        },
        {
            "id": "MONDO:0008148",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008148",
            "name": "osteogenesis imperfecta, type 4",
            "description": ""
        },
        {
            "id": "MONDO:0008148",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008148",
            "name": "OI, type 4",
            "description": ""
        },
        {
            "id": "MONDO:0008148",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008148",
            "name": "osteogenesis imperfecta with normal sclerae",
            "description": ""
        },
        {
            "id": "MONDO:0008148",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008148",
            "name": "OI type IV",
            "description": ""
        },
        {
            "id": "MONDO:0008148",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008148",
            "name": "OI4",
            "description": ""
        },
        {
            "id": "MONDO:0008148",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008148",
            "name": "osteogenesis imperfecta, type IV",
            "description": ""
        },
        {
            "id": "MIM:616507",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/616507",
            "name": "Osteogenesis imperfecta 17",
            "description": "Osteogenesis imperfecta 17"
        },
        {
            "id": "MIM:616507",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/616507",
            "name": "Osteogenesis imperfecta 17",
            "description": "Osteogenesis imperfecta 17"
        }
    ]
}