t(10;17)(q22;p13)

Preferred Label : t(10;17)(q22;p13);

NCIt definition : A cytogenetic abnormality that refers to the translocation of the long arm (q22) of chromosome 10 and the short arm (p13) of chromosome 17. It results in an YWHAE-FAM22 fusion. It has been described in high grade endometrial stromal sarcomas and a subset of clear cell sarcomas of the kidney.;

NCI Metathesaurus CUI : CL508106;

Détails

Origin ID

C127049;

UMLS CUI

C4287950;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 10 [NCIt concept]
- Human Chromosome 17 [NCIt concept]
is_cytogenetic_abnormality_of_disease
- Uterine Corpus High Grade Endometrial Stromal Sarcoma [NCIt concept]
is_not_cytogenetic_abnormality_of_disease
- Endometrial Stromal Nodule [NCIt concept]
- Uterine Corpus Low Grade Endometrial Stromal Sarcoma [NCIt concept]
- Uterine Corpus Tumor Resembling Ovarian Sex Cord Tumor [NCIt concept]
- Uterine Corpus Undifferentiated Sarcoma [NCIt concept]
may_be_cytogenetic_abnormality_of_disease
- Clear Cell Sarcoma of the Kidney [NCIt concept]

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