t(4;11)(q21;q23.3)

Preferred Label : t(4;11)(q21;q23.3);

NCIt synonyms : t 4 11 q21 q23;

NCIt related terms : t(4;11)(q21;q23);

NCIt definition : A chromosomal abnormality consisting of the translocation of 4q21 with 11q23.3.;

Details

Origin ID

C36365;

UMLS CUI

C1515769;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
concept_is_in_subset
- ALL Authorized Value Terminology [NCIt concept]
- ALL Molecular Analysis Table [NCIt concept]
- 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]
- Human Chromosome 4 [NCIt concept]
is_abnormality_of_gene
- MLL/AFF1 Fusion Gene [NCIt concept]
is_cytogenetic_abnormality_of_disease
- Acute Myeloid Leukemia with t(4;11)(q21.3;q23.3); AFF1-KMT2A [NCIt concept]
- B Acute Lymphoblastic Leukemia with t(4;11)(q21;23.3); KMT2A-AFF1 [NCIt concept]
molecular_abnormality_involves_gene
- AFF1 Gene [NCIt concept]
- KMT2A Gene [NCIt concept]
- MLL/AFF1 Fusion Gene [NCIt concept]

Keyword's position in hierarchy(ies) :

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