About: t(11;19)(q23;p13.1)     Goto   Sponge   NotDistinct   Permalink

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AttributesValues
rdf:type
rdfs:label
  • t(11;19)(q23;p13.1)
rdfs:subClassOf
Semantic_Type
  • Cell or Molecular Dysfunction
Preferred_Name
  • t(11;19)(q23;p13.1)
UMLS_CUI
  • C1515710
Legacy_Concept_Name
  • t_11_19_q23_p13_1
FULL_SYN
  • t(11;19)(q23;p13.1)PTNCI
DEFINITION
  • A cytogenetic abnormality that refers to the translocation of the long arm (q23) of chromosome 11 and the short arm (p13.1) of chromosome 19. It is associated with the development of acute myeloid leukemia with variant MLL translocations and topoisomerase II inhibitor-related acute myeloid leukemia.NCI
code
  • C36371
is someValuesFrom of
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