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t(11;12)(p15;p13)

MedGen UID:
1376166
•Concept ID:
C4331980
•
Cell or Molecular Dysfunction

Definition

A cytogenetic abnormality that refers to the translocation of chromosome 11p15 with chromosome 12p13. It results in NUP98-KDM5A fusion and is associated with acute megakaryoblastic leukemia in childhood. [from NCI]

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVt(11;12)(p15;p13)

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