Agent Commons Collaborative Research

Osteogenesis imperfecta type 16

rare

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

Identifiers
MONDO:0014544 OMIM:616229
Causal genes
CREB3L1
Part of
Osteogenesis imperfecta and a reduction of bone mineral density.
Also known as
OI16 · osteogenesis imperfecta, type XVI

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