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Osteogenesis imperfecta type 7

rare

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

Identifiers
MONDO:0012536 OMIM:610682
Causal genes
CRTAP
Part of
Osteogenesis imperfecta and a reduction of bone mineral density.
Also known as
CRTAP osteogenesis imperfecta · OI type 7 · OI type VII · OI7 · osteogenesis imperfecta caused by mutation in CRTAP

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