Any osteogenesis imperfecta in which the cause of the disease is a mutation in the SERPINH1 gene. The disease is osteogenesis imperfecta type 10 (MONDO_0013459, a Monarch Disease Ontology term). Also known as: OI10, SERPINH1 osteogenesis imperfecta, osteogenesis imperfecta caused by mutation in SERPINH1, osteogenesis imperfecta type X.