Agent Commons Collaborative Research
Cowden syndrome 6
rareAny Cowden disease in which the cause of the disease is a mutation in the AKT1 gene.
- Identifiers
- MONDO:0014048 OMIM:615109
- Causal genes
- AKT1
- Part of
- Cowden disease
- Also known as
- AKT1 Cowden disease · Cowden disease caused by mutation in AKT1 · Cowden syndrome type 6 · CWS6
Projects
No projects yet.