Terminology Service for NFDI4Health

t(11;19)(q23;p13.1)

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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. [ ]

Term info

Label

t(11;19)(q23;p13.1)

Synonyms
  • t(11;19)(q23;p13.1)
Legacy Concept Name

t_11_19_q23_p13_1

Preferred Name

t(11;19)(q23;p13.1)

Semantic Type

Cell or Molecular Dysfunction

UMLS CUI

C1515710

code

C36371