Osteogenesis imperfecta type 10

MONDO:0013459

Any osteogenesis imperfecta in which the cause of the disease is a mutation in the SERPINH1 gene.

Also known as: OI10, SERPINH1 osteogenesis imperfecta, osteogenesis imperfecta caused by mutation in SERPINH1, OI type 10, OI type X, OI, type 10, osteogenesis imperfecta, type 10, osteogenesis imperfecta, type X

0 clinical trials for this condition and its sub-types, 0 tagged with Osteogenesis imperfecta type 10 itself.

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Part of

↑ Osteogenesis imperfecta and a reduction of bone mineral density. (307)

Including sub-types (0) Tagged with Osteogenesis imperfecta type 10 (0)

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