Bruck syndrome 2

MONDO:0012217

Any Bruck syndrome in which the cause of the disease is a mutation in the PLOD2 gene.

Also known as: Bruck syndrome 2, Bruck syndrome caused by mutation in PLOD2, Bruck syndrome type 2, PLOD2 Bruck syndrome, BRKS2, osteogenesis imperfecta with congenital Joint contractures

0 clinical trials for this condition and its sub-types, 0 tagged with Bruck syndrome 2 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) ↑ Bruck syndrome (0)

Including sub-types (0) Tagged with Bruck syndrome 2 (0)

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