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t(11;17)(q23;q12-21)

MedGen UID:: 1712896
•Concept ID:: C5239095
•: Cell or Molecular Dysfunction

Definition

A cytogenetic abnormality that refers to the translocation of the long arm (q23) of chromosome 11 and the long arm (q12-21) of chromosome 19. It is associated with KMT2A (MLL) fusions, including those with MLLT6 (AF17), and acute myeloid leukemia. [from NCI]

Term Hierarchy

GTR
MeSH

CClinical test, RResearch test, OOMIM, GGeneReviews, VClinVar

CROGVt(11;17)(q23;q12-21)

Molecular Abnormality
- Cytogenetic Abnormality
  - Chromosome 17 disorder
    - t(11;17)(q23;q12-21)

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