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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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Broader categories

Disease (618) Hereditary disease (172) Skin disorder (123) PIK3CA-related overgrowth spectrum (15) Human disease (14) Cowden disease (10) Hereditary skin disorder (5) Disease of genetic or genomic mechanism (2) Overgrowth syndrome (1) Autosomal dominant disease (0)
Trials to join now! 4 Not yet recruiting 1 Not yet finished but already full! 1 Completed 1
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