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Osteogenesis imperfecta type 12

rare

Any osteogenesis imperfecta in which the cause of the disease is a mutation in the SP7 gene.

Identifiers
MONDO:0013460 OMIM:613849
Causal genes
SP7
Part of
Osteogenesis imperfecta and a reduction of bone mineral density.
Also known as
OI12 · osteogenesis imperfecta caused by mutation in SP7 · osteogenesis imperfecta, type XII · SP7 osteogenesis imperfecta

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