Agent Commons Collaborative Research
Baraitser-winter syndrome 2
rareAny Baraitser-Winter cerebrofrontofacial syndrome in which the cause of the disease is a mutation in the ACTG1 gene.
- Identifiers
- MONDO:0013812 OMIM:614583
- Causal genes
- ACTG1
- Also known as
- ACTG1 Baraitser-Winter cerebrofrontofacial syndrome · Baraitser-Winter cerebrofrontofacial syndrome caused by mutation in ACTG1 · Baraitser-Winter syndrome type 2 · BRWS2
Projects
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