About: MUTYH-Associate Polyposis     Goto   Sponge   NotDistinct   Permalink

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AttributesValues
rdf:type
rdfs:label
  • MUTYH-Associate Polyposis
equivalentClass
Semantic_Type
  • Disease or Syndrome
Preferred_Name
  • MUTYH-Associate Polyposis
NCI_META_CUI
  • CL429230
FULL_SYN
  • MUTYH-Associate PolyposisPTNCI
  • MAPABNCI
DEFINITION
  • An autosomal recessive hereditary neoplastic syndrome caused by mutations in the MUTYH gene on chromosome 1p34.1. It is characterized by the presence of multiple colorectal polyps that may progress to carcinoma. Development of gastric and small intestinal polyps may also occur.NCI
code
  • C96520
is someValuesFrom of
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