t(v;11q23.3) - CISMeF

Preferred Label : t(v;11q23.3);

NCIt synonyms : t(11;v)(q23;v); t 11 v q23 v; t(V;11)(v;q23.3); t(11;v)(q23.3;v); t(V;11)(v;q23); 11q23.3 Translocation;

NCIt related terms : MLL Other Partner;

NCIt definition : A chromosomal abnormality consisting of the translocation of genetic material from any one of several chromosomes to the 11q23.3 region, resulting in an MLL gene rearrangement.;

Details

Origin ID

C36517;

UMLS CUI

C1515714;

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]
- CTRP Biomarker Terminology [NCIt concept]
- CTRP Molecular Genetic Biomarker Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 11 [NCIt concept]
is_cytogenetic_abnormality_of_disease
- B Acute Lymphoblastic Leukemia with t(4;11)(q21;23.3); KMT2A-AFF1 [NCIt concept]
- B Acute Lymphoblastic Leukemia with t(v;11q23.3); KMT2A Rearranged [NCIt concept]
- B Lymphoblastic Leukemia/Lymphoma with t(v;11q23.3); KMT2A Rearranged [NCIt concept]
- Mixed Phenotype Acute Leukemia with KMT2A Rearrangement [NCIt concept]
is_not_cytogenetic_abnormality_of_disease
- Mixed Phenotype Acute Leukemia, B/Myeloid [NCIt concept]
- Mixed Phenotype Acute Leukemia, T/Myeloid [NCIt concept]
molecular_abnormality_involves_gene
- KMT2A Gene [NCIt concept]

Keyword's position in hierarchy(ies) :

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