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

0 clinical trials for this condition and its sub-types, 0 tagged with Cowden syndrome 2 itself.

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