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Cowden syndrome 2

MONDO:0012878

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

Also known as: Cowden disease caused by mutation in SDHB, Cowden syndrome 2, Cowden syndrome type 2, SDHB Cowden disease, CWS2

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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