t(9;22) - CISMeF

Preferred Label : t(9;22);

NCIt definition : A translocation between chromosome 9 and chromosome 22 that may be associated with Philadelphia chromosome and increased susceptibility to several types of leukemia.;

Details

Origin ID

C117116;

UMLS CUI

C3897138;

Currated CISMeF NLP mapping
- t(9;22) [EMDN type]
Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
concept_is_in_subset
- ALL Authorized Value Terminology [NCIt concept]
- ALL Molecular Analysis Table [NCIt concept]
- CPTAC Acute Myeloid Leukemia Baseline Form [NCIt concept]
- CPTAC Baseline Medical Forms Terminology [NCIt concept]
- CPTAC Terminology [NCIt concept]
- CTRP Biomarker Terminology [NCIt concept]
- CTRP Molecular Genetic Biomarker Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
- GDC Terminology [NCIt concept]
- GDC Value Terminology [NCIt concept]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 22 [NCIt concept]
- Human Chromosome 9 [NCIt concept]

Keyword's position in hierarchy(ies) :

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