t(11;19)(q23.3;p13.1)

Preferred Label : t(11;19)(q23.3;p13.1);

NCIt synonyms : t 11 19 q23 p13 1;

NCIt related terms : t(11;19)(q23;p13.1);

NCIt definition : A cytogenetic abnormality that refers to the translocation of the long arm (q23.3) 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.;

Details

Origin ID

C36371;

UMLS CUI

C1515710;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
UMLS correspondences (same concept)
- t(11;19)(q23;p13.1)(MLL,ELL) [LOINC component]
concept_is_in_subset
- AML Authorized Value Terminology [NCIt concept]
- AML Minimal Residual Disease Table [NCIt concept]
- AML Molecular Analysis Table [NCIt concept]
- GDC Terminology [NCIt concept]
- GDC Value Terminology [NCIt concept]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 11 [NCIt concept]
- Human Chromosome 19 [NCIt concept]
is_cytogenetic_abnormality_of_disease
- Acute Myeloid Leukemia with t(11;19)(q23.3;p13.1); KMT2A-ELL [NCIt concept]
may_be_cytogenetic_abnormality_of_disease
- Topoisomerase II Inhibitor-Related Acute Myeloid Leukemia [NCIt concept]
molecular_abnormality_involves_gene
- KMT2A Gene [NCIt concept]

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