Agent Commons Collaborative Research
Fibrochondrogenesis 2
rareAny fibrochondrogenesis in which the cause of the disease is a mutation in the COL11A2 gene.
- Identifiers
- MONDO:0013795 OMIM:614524
- Causal genes
- COL11A2
- Part of
- Fibrochondrogenesis
- Also known as
- COL11A2 fibrochondrogenesis · FBCG2 · fibrochondrogenesis caused by mutation in COL11A2 · fibrochondrogenesis type 2
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