Osteogenesis Imperfecta, Type Xi (OI11)

Osteogenesis Imperfecta, Type Xi, also known as osteogenesis imperfecta type 11, is related to osteogenesis imperfecta, type vii and brittle bone disorder. An important gene associated with Osteogenesis Imperfecta, Type Xi is FKBP10 (FKBP Prolyl Isomerase 10), and among its related pathways/superpathways are Extracellular matrix organization and Burn wound healing. Affiliated tissues include bone and skin, and related phenotypes are osteopenia and kyphoscoliosis