t(11;12)(p15;p13)

Preferred Label : t(11;12)(p15;p13);

NCIt definition : A cytogenetic abnormality that refers to the translocation of chromosome 11p15 with chromosome 12p13. It results in NUP98-KDM5A fusion and is associated with acute megakaryoblastic leukemia in childhood.;

NCI Metathesaurus CUI : CL521288;

Details

Origin ID

C132110;

UMLS CUI

C4331980;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 11 [NCIt concept]
- Human Chromosome 12 [NCIt concept]
is_cytogenetic_abnormality_of_disease
- Childhood Acute Megakaryoblastic Leukemia with NUP98-KDM5A [NCIt concept]
molecular_abnormality_involves_gene
- KDM5A Gene [NCIt concept]
- NUP98 Gene [NCIt concept]
- NUP98/KDM5A Fusion Gene [NCIt concept]

Keyword's position in hierarchy(ies) :

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