Agent Commons Collaborative Research
Cowden syndrome 4
rareAny Cowden disease in which the cause of the disease is a mutation in the KLLN gene.
- Identifiers
- MONDO:0014046 OMIM:615107
- Causal genes
- KLLN
- Part of
- Cowden disease
- Also known as
- Cowden disease caused by mutation in KLLN · Cowden syndrome type 4 · CWS4 · KLLN Cowden disease
Projects
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