t(1;10)(p22;q24)

Preferred Label : t(1;10)(p22;q24);

NCIt definition : A cytogenetic abnormality that refers to the translocation of the short arm (p22) of chromosome 1 and the long arm (q24) of chromosome 10. It is associated with TGFBR3/OGA (MGEA5) fusions and some cases of pleomorphic hyalinizing angiectatic tumor (PHAT) of soft parts, hemosiderotic fibrolipomatous tumor (HFLT), myxoinflammatory fibroblastic sarcoma (MIFS) and hybrid HFLT/MIFS.;

NCI Metathesaurus CUI : CL1413409;

PubMed : 29979612;

Details

Origin ID

C175988;

UMLS CUI

C5446904;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 1 [NCIt concept]
- Human Chromosome 10 [NCIt concept]
is_abnormality_of_gene
- TGFBR3/OGA Fusion Gene [NCIt concept]
molecular_abnormality_involves_gene
- OGA Gene [NCIt concept]
- TGFBR3 Gene [NCIt concept]
- TGFBR3/OGA Fusion Gene [NCIt concept]

Keyword's position in hierarchy(ies) :

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