t(5;11)(q35;p15)

Preferred Label : t(5;11)(q35;p15);

NCIt definition : A cytogenetic abnormality that refers to the translocation of chromosome 11p15 with chromosome 5q35. It results in the formation of NUP98/NSD1 fusion gene. It is associated with the development of acute myeloid leukemia with t(5;11)(q35;p15); NUP98-NSD1.;

NCI Metathesaurus CUI : CL514691;

Détails

Origin ID

C131503;

UMLS CUI

C4331808;

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]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 11 [NCIt concept]
- Human Chromosome 5 [NCIt concept]
is_cytogenetic_abnormality_of_disease
- Childhood Acute Myeloid Leukemia with t(5;11)(q35;p15); NUP98-NSD1 [NCIt concept]
molecular_abnormality_involves_gene
- NSD1 Gene [NCIt concept]
- NSD1/NUP98 Fusion Gene [NCIt concept]
- NUP98 Gene [NCIt concept]

Position du mot-clé dans l'(les) arborescence(s) :

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