bn:01949086n
Noun Concept
Categories: Syndromes affecting the breast, Deficiencies of intracellular signaling peptides and proteins, Epidermal nevi, neoplasms, cysts, Syndromes affecting the gastrointestinal tract, Hereditary cancers
EN
Cowden syndrome  Cowden syndrome 1  Lhermitte-Duclos disease  Cowden's disease  Cowden's syndrome
EN
Cowden syndrome is an autosomal dominant inherited condition characterized by benign overgrowths called hamartomas as well as an increased lifetime risk of breast, thyroid, uterine, and other cancers. Wikipedia
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EN
Cowden syndrome is an autosomal dominant inherited condition characterized by benign overgrowths called hamartomas as well as an increased lifetime risk of breast, thyroid, uterine, and other cancers. Wikipedia
A rare autosomal dominant inherited disorder Wikipedia Disambiguation
Inherited disorder causing tumor-like growth and increased cancer risk Wikidata