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Cowden syndrome 4

MONDO:0014046

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

Also known as: Cowden disease caused by mutation in KLLN, Cowden syndrome 4, Cowden syndrome type 4, KLLN Cowden disease, CWS4

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

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Broader categories

Disease (680) Hereditary disease (176) Skin disorder (132) Human disease (14) Cowden disease (11) Hereditary skin disorder (6) Disease of genetic or genomic mechanism (2) Autosomal dominant disease (0) Autosomal genetic disease (0) Disease by body system or component (0)

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