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

0 clinical trials for this condition and its sub-types, 0 tagged with Cowden syndrome 7 itself.

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