Fibrochondrogenesis 1

MONDO:0009226

Any fibrochondrogenesis in which the cause of the disease is a mutation in the COL11A1 gene.

Also known as: COL11A1 fibrochondrogenesis, fibrochondrogenesis 1, fibrochondrogenesis caused by mutation in COL11A1, fibrochondrogenesis type 1, FBCG1

0 clinical trials for this condition and its sub-types, 0 tagged with Fibrochondrogenesis 1 itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Fibrochondrogenesis (0)

Including sub-types (0) Tagged with Fibrochondrogenesis 1 (0)

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