t(X;18) - CISMeF

Preferred Label : t(X;18);

NCIt definition : A translocation between the X chromosome and chromosome 18.;

NCI Metathesaurus CUI : CL1920724;

Details

Origin ID

C201851;

UMLS CUI

C5908209;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
concept_is_in_subset
- CTRP Biomarker Terminology [NCIt concept]
- CTRP Molecular Genetic Biomarker Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 18 [NCIt concept]
- Human Chromosome X [NCIt concept]

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