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

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CISMeF

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

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03/07/2025

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