Osteogenesis Imperfecta Type V

About the Disease
Osteogenesis Imperfecta, Type V, also known as osteogenesis imperfecta type 5, is related to osteogenesis imperfecta, type vi and brittle bone disorder. An important gene associated with Osteogenesis Imperfecta, Type V is IFITM5 (Interferon Induced Transmembrane Protein 5), and among its related pathways/superpathways are Binding and Uptake of Ligands by Scavenger Receptors and NRP1-triggered signaling pathways in pancreatic cancer. Affiliated tissues include bone, and related phenotypes are joint hypermobility and osteopenia

Common Targets
IFITM5

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