Osteogenesis imperfecta type 16

MONDO:0014544

An osteogenesis imperfecta that has material basis in contiguous gene deletion on chromosome 11p11.

Also known as: OI16, OI, type 16, chromosome 11P11.2 deletion syndrome, 91.3-Kb, osteogenesis imperfecta, type 16, osteogenesis imperfecta, type XVI

0 clinical trials for this condition and its sub-types, 0 tagged with Osteogenesis imperfecta type 16 itself.

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