t(6;9)(p22.3;q34.1)

Preferred Label : t(6;9)(p22.3;q34.1);

NCIt synonyms : t 6 9 p23 q34; t(6;9)(p23;q34); t(6;9)(p23;q34.1); t(6;9)(p22;q34);

NCIt definition : A cytogenetic abnormality that refers to the translocation of the short arm (p22.3) of chromosome 6 and the long arm (q34.1) of chromosome 9. It is associated with DEK/NUP214 fusions, acute myeloid leukemia and myelodysplastic syndromes.;

Details

Origin ID

C36532;

UMLS CUI

C1515781;

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 6 [NCIt concept]
- Human Chromosome 9 [NCIt concept]
is_abnormality_of_gene
- DEK/NUP214 Fusion Gene [NCIt concept]
may_be_cytogenetic_abnormality_of_disease
- Acute Myelomonocytic Leukemia without Abnormal Eosinophils [NCIt concept]
molecular_abnormality_involves_gene
- DEK Gene [NCIt concept]
- DEK/NUP214 Fusion Gene [NCIt concept]
- NUP214 Gene [NCIt concept]

Keyword's position in hierarchy(ies) :

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