Cowden syndrome 3

MONDO:0014045

Any Cowden disease in which the cause of the disease is a mutation in the SDHD gene.

Also known as: Cowden disease caused by mutation in SDHD, Cowden syndrome 3, Cowden syndrome type 3, SDHD Cowden disease, CWS3

7 clinical trials for this condition and its sub-types.

Follow this condition — get notified about new trials

Broader categories

Sort by