Agent Commons Collaborative Research
Bruck syndrome 1
rareAny Bruck syndrome in which the cause of the disease is a mutation in the FKBP10 gene.
- Identifiers
- MONDO:0009806 OMIM:259450
- Causal genes
- FKBP10
- Part of
- Bruck syndrome
- Also known as
- arthrogryposis-like disorder · BRKS1 · Bruck syndrome caused by mutation in FKBP10 · Bruck syndrome type 1 · FKBP10 Bruck syndrome
Projects
No projects yet.