Osteogenesis imperfecta type 7

MONDO:0012536

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

Also known as: CRTAP osteogenesis imperfecta, OI7, osteogenesis imperfecta caused by mutation in CRTAP, osteogenesis imperfecta type 7, OI type 7, OI type VII, OI, type 7, osteogenesis imperfecta, type 7

0 clinical trials for this condition and its sub-types, 0 tagged with Osteogenesis imperfecta type 7 itself.

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Part of

↑ Osteogenesis imperfecta and a reduction of bone mineral density. (308)

Including sub-types (0) Tagged with Osteogenesis imperfecta type 7 (0)

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