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t(9;11)(p21.3;q23.3)

Go to external page http://purl.obolibrary.org/obo/NCIT_C36370

A cytogenetic abnormality that refers to the translocation of the short arm (p21.3) of chromosome 9 and the long arm (q23.3) of chromosome 11. It is associated with the development of acute myeloid leukemia with the MLLT3-MLL fusion gene transcript. [ ]

Term info

Label

t(9;11)(p21.3;q23.3)

Synonyms
  • t(9;11)(p21.3;q23.3)
  • t(9;11)(p22;q23)
Legacy Concept Name

t_9_11_p22_q23

Preferred Name

t(9;11)(p21.3;q23.3)

Semantic Type

Cell or Molecular Dysfunction

UMLS CUI

C1515800

code

C36370