t(X;18)(p11.2-q11.2)

Preferred Label : t(X;18)(p11.2-q11.2);

NCIt definition : A cytogenetic abnormality that refers to a chromosomal translocation that involves the short arm (p11.2) of the X chromosome and the long arm (q11.2) of chromosome 18. It is associated with the expression of SS18/SSX4 fusions and the development of synovial sarcoma.;

NCI Metathesaurus CUI : CL1920725;

Details

Origin ID

C201852;

UMLS CUI

C5908210;

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]
is_abnormality_of_gene
- SS18/SSX4 Fusion Gene [NCIt concept]
molecular_abnormality_involves_gene
- SS18 Gene [NCIt concept]
- SS18/SSX4 Fusion Gene [NCIt concept]
- SSX4 Gene [NCIt concept]

Keyword's position in hierarchy(ies) :

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