t(11;15)(p15;q35)

Preferred Label : t(11;15)(p15;q35);

NCIt definition : A cytogenetic abnormality that refers to the translocation of chromosome 11p15 with chromosome 15q35. It results in the formation of NUP98/JARID1A fusion gene. It is associated with the development of acute myeloid leukemia with t(11;15)(p15;q35); NUP98-JARID1A.;

NCI Metathesaurus CUI : CL514689;

Détails

Origin ID

C131505;

UMLS CUI

C4331807;

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 15 [NCIt concept]
is_cytogenetic_abnormality_of_disease
- Childhood Acute Myeloid Leukemia with t(11;15)(p15;q35); NUP98-JARID1A [NCIt concept]
molecular_abnormality_involves_gene
- KDM5A Gene [NCIt concept]
- NUP98 Gene [NCIt concept]
- NUP98/KDM5A Fusion Gene [NCIt concept]

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

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