Osteogenesis imperfecta type 8

MONDO:0012581

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

Also known as: OI8, P3H1 osteogenesis imperfecta, osteogenesis imperfecta caused by mutation in P3H1, osteogenesis imperfecta type 8, OI type VIII, OI, type 8, osteogenesis imperfecta, type 8, osteogenesis imperfecta, type VIII

0 clinical trials for this condition and its sub-types, 0 tagged with Osteogenesis imperfecta type 8 itself.

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Part of

↑ Osteogenesis imperfecta and a reduction of bone mineral density. (308)

Including sub-types (0) Tagged with Osteogenesis imperfecta type 8 (0)

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