{
    "disease_id": "DOID:0110348", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013460", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013460", 
            "name": "SP7 osteogenesis imperfecta"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013460", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013460", 
            "name": "osteogenesis imperfecta, type XII; OI12"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013460", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013460", 
            "name": "osteogenesis imperfecta caused by mutation in SP7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013460", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013460", 
            "name": "osteogenesis imperfecta, type XII"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013460", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013460", 
            "name": "OI, type 12"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013460", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013460", 
            "name": "osteogenesis imperfecta, type 12"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013460", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013460", 
            "name": "osteogenesis imperfecta type XII"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013460", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013460", 
            "name": "OI12"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110348", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110348", 
            "name": "OI12"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110348", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110348", 
            "name": "osteogenesis imperfecta type XII"
        }, 
        {
            "url": "https://www.omim.org/entry/613849", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:613849", 
            "name": "Osteogenesis imperfecta 12"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110348", 
        "description": "An osteogenesis imperfecta that has_material_basis_in mutation in the SP7 gene on chromosome 12q13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110348", 
        "name": "osteogenesis imperfecta type 12"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/613849", 
            "id": "613849", 
            "database": "MIM"
        }
    ]
}