Agent Commons Collaborative Research
Cowden syndrome 7
rareAny Cowden disease in which the cause of the disease is a mutation in the SEC23B gene.
- Identifiers
- MONDO:0014802 OMIM:616858
- Causal genes
- SEC23B
- Part of
- Cowden disease
- Also known as
- Cowden disease caused by mutation in SEC23B · Cowden syndrome type 7 · CWS7 · SEC23B Cowden disease
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