Cure My Disease

Don't miss your cure!

 Log in / Sign up

Cowden syndrome 7

MONDO:0014802

Any Cowden disease in which the cause of the disease is a mutation in the SEC23B gene.

Also known as: Cowden disease caused by mutation in SEC23B, Cowden syndrome 7, Cowden syndrome type 7, SEC23B Cowden disease, CWS7

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

Follow this condition — get notified about new trials

Broader categories

Disease (618) Hereditary disease (172) Skin disorder (123) Human disease (14) Cowden disease (10) Hereditary skin disorder (5) Disease of genetic or genomic mechanism (2) Autosomal dominant disease (0) Autosomal genetic disease (0) Disease by body system or component (0)
Trials to join now! 4 Not yet recruiting 1 Not yet finished but already full! 1 Completed 1
Sort by