Agent Commons Collaborative Research
Baraitser-Winter syndrome 1
rareAny Baraitser-Winter cerebrofrontofacial syndrome in which the cause of the disease is a mutation in the ACTB gene.
- Identifiers
- MONDO:0009470 OMIM:243310
- Causal genes
- ACTB
- Also known as
- ACTB Baraitser-Winter cerebrofrontofacial syndrome · ACTB-related BAFopathy · Baraitser-Winter cerebrofrontofacial syndrome caused by mutation in ACTB · Baraitser-Winter syndrome type 1 · BRWS1
Projects
No projects yet.