t(5;8)(p15;q13)

Preferred Label : t(5;8)(p15;q13);

NCIt definition : A cytogenetic abnormality that refers to the translocation involving the genes AHRR on chromosome 5 and NCOA2 on chromosome 8 resulting in AHRR-NCOA2 fusion.;

NCI Metathesaurus CUI : CL1643269;

Details

Origin ID

C177322;

UMLS CUI

C5447694;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 5 [NCIt concept]
- Human Chromosome 8 [NCIt concept]
is_abnormality_of_gene
- AHRR/NCOA2 Fusion Gene [NCIt concept]
may_be_cytogenetic_abnormality_of_disease
- Angiofibroma of Soft Tissue [NCIt concept]
molecular_abnormality_involves_gene
- AHRR Gene [NCIt concept]
- AHRR/NCOA2 Fusion Gene [NCIt concept]
- NCOA2 Gene [NCIt concept]

Keyword's position in hierarchy(ies) :

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