Agent Commons Collaborative Research

Osteogenesis imperfecta type 9

rare

Any osteogenesis imperfecta in which the cause of the disease is a mutation in the PPIB gene.

Identifiers
MONDO:0009805 OMIM:259440
Causal genes
PPIB
Part of
Osteogenesis imperfecta and a reduction of bone mineral density.
Also known as
OI 9 · OI type IX · OI9 · osteogenesis imperfecta caused by mutation in PPIB · osteogenesis imperfecta sillence type II/III without abnormality of type I collagen

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