{
    "disease_id": "DOID:0110346",
    "recommended_name": {
        "id": "DOID:0110346",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110346",
        "name": "osteogenesis imperfecta type 10",
        "description": "An osteogenesis imperfecta that has_material_basis_in mutation in the SERPINH gene on chromosome 11q13."
    },
    "synonyms": [
        {
            "id": "DOID:0110346",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110346",
            "name": "OI10",
            "description": ""
        },
        {
            "id": "DOID:0110346",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110346",
            "name": "osteogenesis imperfecta type X",
            "description": ""
        },
        {
            "id": "MONDO:0013459",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013459",
            "name": "osteogenesis imperfecta type 10",
            "description": "Any osteogenesis imperfecta in which the cause of the disease is a mutation in the SERPINH1 gene."
        },
        {
            "id": "MONDO:0013459",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013459",
            "name": "OI type 10",
            "description": ""
        },
        {
            "id": "MONDO:0013459",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013459",
            "name": "OI10",
            "description": ""
        },
        {
            "id": "MONDO:0013459",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013459",
            "name": "SERPINH1 osteogenesis imperfecta",
            "description": ""
        },
        {
            "id": "MONDO:0013459",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013459",
            "name": "OI type X",
            "description": ""
        },
        {
            "id": "MONDO:0013459",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013459",
            "name": "osteogenesis imperfecta, type X; OI10",
            "description": ""
        },
        {
            "id": "MONDO:0013459",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013459",
            "name": "osteogenesis imperfecta caused by mutation in SERPINH1",
            "description": ""
        },
        {
            "id": "MONDO:0013459",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013459",
            "name": "osteogenesis imperfecta, type X",
            "description": ""
        },
        {
            "id": "MONDO:0013459",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013459",
            "name": "OI, type 10",
            "description": ""
        },
        {
            "id": "MONDO:0013459",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013459",
            "name": "osteogenesis imperfecta, type 10",
            "description": ""
        },
        {
            "id": "MONDO:0013459",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013459",
            "name": "osteogenesis imperfecta type X",
            "description": ""
        },
        {
            "id": "MIM:613848",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/613848",
            "name": "Osteogenesis imperfecta 10",
            "description": "Osteogenesis imperfecta 10"
        }
    ]
}