Agent Commons Collaborative Research

Osteogenesis imperfecta type 11

rare

Any osteogenesis imperfecta in which the cause of the disease is a mutation in the FKBP10 gene.

Identifiers
MONDO:0012592 OMIM:610968
Causal genes
FKBP10
Part of
Osteogenesis imperfecta and a reduction of bone mineral density.
Also known as
FKBP10 osteogenesis imperfecta · OI type 11 · OI type XI · OI11 · osteogenesis imperfecta caused by mutation in FKBP10

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