{
    "disease_id": "DOID:0110341", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008147", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008147", 
            "name": "osteogenesis imperfecta congenita"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008147", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008147", 
            "name": "osteogenesis imperfecta type II"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008147", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008147", 
            "name": "Vrolik type of osteogenesis imperfecta"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008147", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008147", 
            "name": "osteogenesis imperfecta, type II; OI2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008147", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008147", 
            "name": "perinatal lethal osteogenesis imperfecta congenita"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008147", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008147", 
            "name": "osteogenesis imperfecta, type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008147", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008147", 
            "name": "OI, type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008147", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008147", 
            "name": "OI2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008147", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008147", 
            "name": "osteogenesis imperfecta, type II"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008147", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008147", 
            "name": "lethal osteogenesis imperfecta"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008147", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008147", 
            "name": "OI type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008147", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008147", 
            "name": "osteogenesis imperfecta congenita, perinatal lethal form"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008147", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008147", 
            "name": "Perinatally lethal OI"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008147", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008147", 
            "name": "osteogenesis imperfecta congenita perinatal lethal form"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110341", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110341", 
            "name": "OI2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110341", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110341", 
            "name": "Vrolik type of osteogenesis imperfecta"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110341", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110341", 
            "name": "osteogenesis imperfecta type II"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110341", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110341", 
            "name": "perinatal lethal osteogenesis imperfecta congenita"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110341", 
        "description": "An osteogenesis imperfecta that is characterized by bone fragility and perinatal lethality and has_material_basis_in dominantly inherited mutations in the COL1A1 gene on chromosome 17q21.33 or the COL1A2 gene on chromosome 7q21.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110341", 
        "name": "osteogenesis imperfecta type 2"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110341#disease-associations", 
            "id": "0110341", 
            "database": "Alliance of Genome Resources"
        }
    ]
}