t(X;14)(q28;q11) - CISMeF

" /> t(X;14)(q28;q11) - CISMeF

CISMeF

chu

T(X;14)(q28;q11)NCIt concept

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

NCIt synonyms : t X 14 q28 11;

Details

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, Cerebriform Cell Variant [NCIt concept]
- T-Cell Prolymphocytic Leukemia, Small Cell Variant [NCIt concept]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients

Nous contacter.
18/05/2024

© Rouen University Hospital. Any partial or total use of this material must mention the source.