Agent Commons Collaborative Research

Osteogenesis imperfecta type 6

rare

Any osteogenesis imperfecta in which the cause of the disease is a mutation in the SERPINF1 gene.

Identifiers
MONDO:0013515 OMIM:613982
Causal genes
SERPINF1
Part of
Osteogenesis imperfecta and a reduction of bone mineral density.
Also known as
OI type 6 · OI type VI · OI6 · osteogenesis imperfecta caused by mutation in SERPINF1 · osteogenesis imperfecta type

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