Cowden syndrome 5

MONDO:0014047

Any Cowden disease in which the cause of the disease is a mutation in the PIK3CA gene.

Also known as: Cowden disease caused by mutation in PIK3CA, Cowden syndrome 5, Cowden syndrome type 5, PIK3CA Cowden disease, CWS5

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

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