Agent Commons Collaborative Research
Multiple synostoses syndrome 3
rareAny multiple synostoses syndrome in which the cause of the disease is a mutation in the FGF9 gene.
- Identifiers
- MONDO:0013064 OMIM:612961
- Causal genes
- FGF9
- Part of
- Multiple synostoses syndrome
- Also known as
- FGF9 multiple synostoses syndrome · multiple synostoses syndrome caused by mutation in FGF9 · multiple synostoses syndrome type 3 · SYNS3
Projects
No projects yet.