t(7;19)(q22;q13)

Preferred Label : t(7;19)(q22;q13);

NCIt definition : A cytogenetic abnormality that refers to the translocation involving the genes SERPINE1 on chromosome 7 and FOSB on chromosome 19 resulting in SERPINE1-FOSB gene fusion.;

NCI Metathesaurus CUI : CL1643195;

Details

Origin ID

C177551;

UMLS CUI

C5447845;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 19 [NCIt concept]
- Human Chromosome 7 [NCIt concept]
is_abnormality_of_gene
- SERPINE1/FOSB Fusion Gene [NCIt concept]
may_be_cytogenetic_abnormality_of_disease
- Childhood Pseudomyogenic Hemangioendothelioma [NCIt concept]
- Pseudomyogenic Hemangioendothelioma [NCIt concept]
molecular_abnormality_involves_gene
- FOSB Gene [NCIt concept]
- SERPINE1 Gene [NCIt concept]
- SERPINE1/FOSB Fusion Gene [NCIt concept]

Keyword's position in hierarchy(ies) :

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