{
    "disease_id": "DOID:0111849",
    "recommended_name": {
        "id": "DOID:0111849",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111849",
        "name": "osteogenesis imperfecta type 20",
        "description": "An osteogenesis imperfecta characterized by osteopenia, skeletal deformity, and both healed and new fractures on radiography that has_material_basis_in homozygous or compound heterozygous mutation in MESD on chromosome 15q25.1."
    },
    "synonyms": [
        {
            "id": "DOID:0111849",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111849",
            "name": "OI20",
            "description": ""
        },
        {
            "id": "DOID:0111849",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111849",
            "name": "osteogenesis imperfecta type XX",
            "description": ""
        },
        {
            "id": "MIM:618644",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/618644",
            "name": "Osteogenesis imperfecta 20",
            "description": "Osteogenesis imperfecta 20"
        }
    ]
}