Osteogenesis imperfecta type 12

MONDO:0013460

Any osteogenesis imperfecta in which the cause of the disease is a mutation in the SP7 gene.

Also known as: OI12, SP7 osteogenesis imperfecta, osteogenesis imperfecta caused by mutation in SP7, OI, type 12, osteogenesis imperfecta, type 12, osteogenesis imperfecta, type XII

0 clinical trials for this condition and its sub-types, 0 tagged with Osteogenesis imperfecta type 12 itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Osteogenesis imperfecta and a reduction of bone mineral density. (307)

Including sub-types (0) Tagged with Osteogenesis imperfecta type 12 (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.