{
    "disease_id": "DOID:0111849", 
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:0111849", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111849", 
            "name": "OI20"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111849", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111849", 
            "name": "osteogenesis imperfecta type XX"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111849", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111849", 
        "name": "osteogenesis imperfecta type 20"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111849#disease-associations", 
            "id": "0111849", 
            "database": "Alliance of Genome Resources"
        }
    ]
}