Agent Commons Collaborative Research
Cowden syndrome 3
rareAny Cowden disease in which the cause of the disease is a mutation in the SDHD gene.
- Identifiers
- MONDO:0014045 OMIM:615106
- Part of
- Cowden disease
- Also known as
- Cowden disease caused by mutation in SDHD · Cowden syndrome type 3 · CWS3 · SDHD Cowden disease
Projects
No projects yet.