t(8;16)(p11.2;p13.3)

Preferred Label : t(8;16)(p11.2;p13.3);

NCIt synonyms : t(8;16)(p11;p13);

NCIt definition : A cytogenetic abnormality that refers to the translocation of the short arm (p11.2) of chromosome 8 and the short arm (p13.3) of chromosome 16. It is associated with KAT6A/CREBBP fusions and acute myeloid leukemia.;

NCI Metathesaurus CUI : CL972419;

Détails

Origin ID

C167194;

UMLS CUI

C5238351;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
concept_is_in_subset
- CTRP Biomarker Terminology [NCIt concept]
- CTRP Molecular Genetic Biomarker Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 16 [NCIt concept]
- Human Chromosome 8 [NCIt concept]
may_be_cytogenetic_abnormality_of_disease
- Acute Monocytic Leukemia [NCIt concept]
- Adult Acute Monocytic Leukemia [NCIt concept]
- Aleukemic Monocytic Leukemia Cutis [NCIt concept]
- Childhood Acute Monocytic Leukemia [NCIt concept]
- Erythrophagocytosis [NCIt concept]
- Hemophagocytosis [NCIt concept]
- Recurrent Acute Monocytic Leukemia [NCIt concept]
- Refractory Acute Monocytic Leukemia [NCIt concept]
molecular_abnormality_involves_gene
- CREBBP Gene [NCIt concept]
- KAT6A Gene [NCIt concept]
- KAT6A/CREBBP Fusion Gene [NCIt concept]

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

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