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Cowden syndrome 6

MONDO:0014048

Any Cowden disease in which the cause of the disease is a mutation in the AKT1 gene.

Also known as: AKT1 Cowden disease, Cowden disease caused by mutation in AKT1, Cowden syndrome 6, Cowden syndrome type 6, CWS6

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

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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
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