{
    "disease_id": "DOID:0111848", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0044329", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0044329", 
            "name": "osteogenesis imperfecta, type 18"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0044329", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0044329", 
            "name": "OI18"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0044329", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0044329", 
            "name": "osteogenesis imperfecta, type XVIII; OI18"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111848", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111848", 
            "name": "OI18"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111848", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111848", 
            "name": "osteogenesis imperfecta, type XVIII"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111848", 
        "description": "An osteogenesis imperfecta characterized by congenital bowing of the long bones, wormian bones, blue sclerae, vertebral collapse, and multiple fractures in the first years of life that has_material_basis_in homozygous or compound heterozygous mutation in TENT5A on chromosome 6q14.1.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111848", 
        "name": "osteogenesis imperfecta type 18"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111848#disease-associations", 
            "id": "0111848", 
            "database": "Alliance of Genome Resources"
        }
    ]
}