t(X;14)(q28;q11)

Preferred Label : t(X;14)(q28;q11);

NCIt synonyms : t X 14 q28 11;

NCIt definition : A chromosomal translocation involving breakpoints within the q28 band on the long arm of the X chromosome and the q11 band on the long arm of chromosome 14. This rearrangement is associated with aberrant expression of the MTCP1 gene and T-cell prolymphocytic leukemia.;

Détails

Origin ID

C36360;

UMLS CUI

C5708866;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 14 [NCIt concept]
- Human Chromosome X [NCIt concept]
may_be_cytogenetic_abnormality_of_disease
- Recurrent T-Cell Prolymphocytic Leukemia [NCIt concept]
- Refractory T-Cell Prolymphocytic Leukemia [NCIt concept]
- Splenic Manifestation of T-Cell Prolymphocytic Leukemia [NCIt concept]
- T-Cell Prolymphocytic Leukemia [NCIt concept]
- T-Cell Prolymphocytic Leukemia Involving the Skin [NCIt concept]
- T-Cell Prolymphocytic Leukemia, Cerebriform Cell Variant [NCIt concept]
- T-Cell Prolymphocytic Leukemia, Small Cell Variant [NCIt concept]
molecular_abnormality_involves_gene
- MTCP1 Gene [NCIt concept]
- T-Cell Receptor Alpha Locus [NCIt concept]
- T-Cell Receptor Gene [NCIt concept]

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

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