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Cowden syndrome 3

MONDO:0014045

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

Also known as: Cowden disease caused by mutation in SDHD, Cowden syndrome 3, Cowden syndrome type 3, SDHD Cowden disease, CWS3

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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