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bn:01949086n
Noun Concept
NL
Cowden syndrome  cowden syndroom
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
Relations
Sources
IS A
syndroom
EN
Multiple hamartoma syndrome
GENETIC ASSOCIATION
Phosphatase and tensin homolog
HEALTH SPECIALTY
oncologie
medische genetica
Wikidata
NL
Cowden syndrome
Wikipedia Translations
NL
cowden syndroom

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