Fibrochondrogenesis 2

MONDO:0013795

Any fibrochondrogenesis in which the cause of the disease is a mutation in the COL11A2 gene.

Also known as: COL11A2 fibrochondrogenesis, fibrochondrogenesis 2, fibrochondrogenesis caused by mutation in COL11A2, fibrochondrogenesis type 2, FBCG2

0 clinical trials for this condition and its sub-types, 0 tagged with Fibrochondrogenesis 2 itself.

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Including sub-types (0) Tagged with Fibrochondrogenesis 2 (0)

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