{
    "disease_id": "DOID:0112201",
    "recommended_name": {
        "id": "DOID:0112201",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0112201",
        "name": "osteogenesis imperfecta type 21",
        "description": "An osteogenesis imperfecta characterized by multiple fractures that often occur after minor trauma, disproportionate short stature, and scoliosis that has_material_basis_in homozygous or compound heterozygous mutation in KDELR2 on chromosome 7p22.1."
    },
    "synonyms": [
        {
            "id": "DOID:0112201",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0112201",
            "name": "OI21",
            "description": ""
        },
        {
            "id": "DOID:0112201",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0112201",
            "name": "osteogenesis imperfecta type XXI",
            "description": ""
        },
        {
            "id": "MONDO:0030861",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030861",
            "name": "osteogenesis imperfecta, type 21",
            "description": ""
        },
        {
            "id": "MONDO:0030861",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030861",
            "name": "OI21",
            "description": ""
        },
        {
            "id": "MONDO:0030861",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030861",
            "name": "osteogenesis imperfecta 21",
            "description": ""
        },
        {
            "id": "MONDO:0030861",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030861",
            "name": "osteogenesis imperfecta, TYPE XXI",
            "description": ""
        },
        {
            "id": "MIM:619131",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/619131",
            "name": "Osteogenesis imperfecta 21",
            "description": "Osteogenesis imperfecta 21"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0112201"
    ],
    "unlinked_id_list": []
}