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hereditary nonpolyposis colorectal neoplasm associated with other malignancies, more commonly of ovarian or uterine origin

AttributesValues
rdf:type
description
  • hereditary nonpolyposis colorectal neoplasm associated with other malignancies, more commonly of ovarian or uterine origin (en)
health specialty
Mondo ID
Mondo ID
health specialty
Mondo ID
  • MONDO_0012249
rdfs:label
  • Cancer colorectal héréditaire sans polypose type 2 (fr)
  • Lynch syndrome II (en)
  • Na Wetin dey cause ampullary cancer (pcm)
skos:prefLabel
  • Cancer colorectal héréditaire sans polypose type 2 (fr)
  • Lynch syndrome II (en)
  • Na Wetin dey cause ampullary cancer (pcm)
name
  • Cancer colorectal héréditaire sans polypose type 2 (fr)
  • Lynch syndrome II (en)
  • Na Wetin dey cause ampullary cancer (pcm)
instance of
instance of
subclass of
subclass of
UniProt disease ID
OMIM ID
UniProt disease ID
  • DI-00551
OMIM ID
  • 609310
skos:altLabel
  • LYNCH2 (en)
  • Lynch II syndrome (en)
  • Syndrome de Lynch b2 (fr)
UMLS CUI
MeSH descriptor ID
MeSH tree code
MeSH descriptor ID
MeSH tree code
UMLS CUI
  • C1333991
MeSH descriptor ID
  • D055847
MeSH tree code
  • C04.700.250.500
  • C16.320.700.250.500
is about of
is main subject of
is main subject of
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