t(8;9)(p22;p24.1)

Preferred Label : t(8;9)(p22;p24.1);

NCIt definition : A cytogenetic abnormality that refers to the translocation of 8p22 and 9p24.1. This translocation results in the fusion of the PCM1 gene and the JAK2 gene.;

NCI Metathesaurus CUI : CL512998;

Details

Origin ID

C129854;

UMLS CUI

C4331810;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 8 [NCIt concept]
- Human Chromosome 9 [NCIt concept]
is_cytogenetic_abnormality_of_disease
- Myeloid/Lymphoid Neoplasms with JAK2 Rearrangement [NCIt concept]

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