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bn:01949086n
Noun Concept
Categories: Hereditary cancers, Rare syndromes, Syndromes affecting the gastrointestinal tract, Epidermal nevi, neoplasms, cysts, Deficiencies of intracellular signaling peptides and proteins
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
Definitions
Relations
Sources
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
IS A
syndrome
Multiple hamartoma syndrome
GENETIC ASSOCIATION
Phosphatase and tensin homolog
HEALTH SPECIALTY
oncology
medical genetics
Wikipedia
EN
Cowden syndrome
Wikidata
EN
Cowden syndrome 1
Wikipedia Redirections
EN
Cowden's disease, Cowden's syndrome, Cowden disease, Cowden Syndrome
Wikidata Alias
EN
Cowden's disease, Cowden disease, Cowden syndrome, dysplastic Gangliocytoma of Cerebellum, Lhermitte-Duclos disease, Multiple hamartoma syndrome

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