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

Preferred Label : t(9;11)(p21.3;q23.3);

NCIt synonyms : t 9 11 p22 q23; t(9;11)(q21;q23); t 9 11 q21 q23;

NCIt related terms : t(9;11)(p22;q23);

NCIt definition : 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.;

Details

Origin ID

C36370;

UMLS CUI

C1515800;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
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 9 [NCIt concept]
is_abnormality_of_gene
- KMT2A/MLLT3 Fusion Gene [NCIt concept]
is_cytogenetic_abnormality_of_disease
- Adult Acute Myeloid Leukemia with t(9;11)(p21.3;q23.3); MLLT3-KMT2A [NCIt concept]
- Childhood Acute Myeloid Leukemia with t(9;11)(p21.3;q23.3); MLLT3-KMT2A [NCIt concept]
- Recurrent Acute Myeloid Leukemia with t(9;11)(p21.3;q23.3); MLLT3-KMT2A [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]
- KMT2A/MLLT3 Fusion Gene [NCIt concept]
- MLLT3 Gene [NCIt concept]

Keyword's position in hierarchy(ies) :

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