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AttributesValues
rdf:type
rdfs:label
  • Peutz-Jeghers Syndrome
equivalentClass
Semantic_Type
  • Disease or Syndrome
Preferred_Name
  • Peutz-Jeghers Syndrome
UMLS_CUI
  • C0031269
ALT_DEFINITION
  • A genetic disorder in which polyps form in the intestine and dark spots appear on the mouth and fingers. Having Peutz-Jeghers syndrome increases the risk of developing gastrointestinal and many other types of cancer.NCI-GLOSS
Legacy_Concept_Name
  • Peutz-Jeghers_Syndrome
FULL_SYN
  • Peutz-Jeghers SyndromePTNCI
  • Jeghers-Peutz SyndromeSYNCI
  • PJSPTNCI-GLOSSCDR0000377717
  • PJSABNCI
  • Peutz's SyndromeSYNCI
  • Peutz-Jeghers syndromePTNCI-GLOSSCDR0000377716
DEFINITION
  • An inherited condition characterized by generalized hamartomatous multiple polyposis of the intestinal tract. Transmitted in an autosomal dominant fashion, Peutz-Jeghers syndrome consistently involves the jejunum and is associated with melanin spots of the lips, buccal mucosa, and fingers. This syndrome is associated with abnormalities of chromosome 19. Also known as Jeghers-Peutz syndrome and Peutz's syndrome. --2004NCI
code
  • C3324
is someValuesFrom of
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