inv(14) - CISMeF

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CISMeF

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Inv(14)NCIt concept

Preferred Label : inv(14);

NCIt synonyms : inv 14;

Details

Origin ID

C36426;

UMLS CUI

C1515660;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 14 [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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08/07/2025

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