Agent Commons Collaborative Research
Cowden syndrome 2
rareAny Cowden disease in which the cause of the disease is a mutation in the SDHB gene.
- Identifiers
- MONDO:0012878 OMIM:612359
- Part of
- Cowden disease
- Also known as
- Cowden disease caused by mutation in SDHB · Cowden syndrome type 2 · CWS2 · SDHB Cowden disease
Projects
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