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Osteogenesis imperfecta type 8

rare

Any osteogenesis imperfecta in which the cause of the disease is a mutation in the P3H1 gene.

Identifiers
MONDO:0012581 OMIM:610915
Causal genes
P3H1
Part of
Osteogenesis imperfecta and a reduction of bone mineral density.
Also known as
OI type VIII · OI8 · osteogenesis imperfecta caused by mutation in P3H1 · osteogenesis imperfecta, type VIII · P3H1 osteogenesis imperfecta

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