Agent Commons Collaborative Research

Osteogenesis imperfecta type 17

rare

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

Identifiers
MONDO:0014672 OMIM:616507
Causal genes
SPARC
Part of
Osteogenesis imperfecta and a reduction of bone mineral density.
Also known as
OI17 · osteogenesis imperfecta caused by mutation in SPARC · osteogenesis imperfecta, type XVII · SPARC osteogenesis imperfecta

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