Osteogenesis Imperfecta Foundation

Funding Profiles

Access available for Technion staff. Please sign in to see the Agency profiles (upper left corner)

Osteogenesis imperfecta (OI) is a genetic disorder characterized by fragile bones that break easily. It is also known as “brittle bone disease.” A person is born with this disorder and is affected throughout his or her life time.
The mission of the OI Foundation is to improve the quality of life for people affected by OI through research to find treatments and a cure, education, awareness, and mutual support.


Contact information:
The fund is not a competitive fund
web site: http://www.oif.org/site/PageServer?pagename=AOI_AboutOI