t(6;11)(q27;q23)

Preferred Label : t(6;11)(q27;q23);

NCIt synonyms : t 6 11 q27 q23; t(6;11)(q27;q23.3);

NCIt definition : A cytogenetic abnormality that refers to the translocation of the long arm (q27) of chromosome 6 and the long arm (q23) of chromosome 11. It is associated with the development of de novo acute myeloid leukemia.;

Détails

Origin ID

C36610;

UMLS CUI

C1515779;

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]
- GDC Terminology [NCIt concept]
- GDC Value Terminology [NCIt concept]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 11 [NCIt concept]
- Human Chromosome 6 [NCIt concept]
is_abnormality_of_gene
- MLL/MLLT4 Fusion Gene [NCIt concept]
is_cytogenetic_abnormality_of_disease
- Acute Myeloid Leukemia with t(6;11)(q27;q23.3); MLLT4-KMT2A [NCIt concept]
molecular_abnormality_involves_gene
- AFDN Gene [NCIt concept]
- KMT2A Gene [NCIt concept]
- MLL/MLLT4 Fusion Gene [NCIt concept]

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

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