Osteogenesis imperfecta type 17
MONDO:0014672Any osteogenesis imperfecta in which the cause of the disease is a mutation in the SPARC gene.
Also known as: OI17, SPARC osteogenesis imperfecta, osteogenesis imperfecta caused by mutation in SPARC, osteogenesis imperfecta, type 17, osteogenesis imperfecta, type XVII
0 clinical trials for this condition and its sub-types, 0 tagged with Osteogenesis imperfecta type 17 itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.