t(12;13)(p13.2;q12.2)

Preferred Label : t(12;13)(p13.2;q12.2);

NCIt definition : A cytogenetic abnormality that refers to the translocation of chromosome 12p13.2 with chromosome 13q12.2. It results in ETV6-FLT3 fusion and is associated with myeloid/lymphoid neoplasms with FLT3-rearrangement.;

NCI Metathesaurus CUI : CL1905742;

Détails

Origin ID

C198561;

UMLS CUI

C5854965;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 12 [NCIt concept]
- Human Chromosome 13 [NCIt concept]
may_be_cytogenetic_abnormality_of_disease
- Myeloid/Lymphoid Neoplasms with FLT3 Rearrangement [NCIt concept]
molecular_abnormality_involves_gene
- ETS Family Gene [NCIt concept]
- ETV6 Gene [NCIt concept]
- ETV6/FLT3 Fusion Gene [NCIt concept]
- FLT3 Gene [NCIt concept]
- Receptor Tyrosine Kinase Gene [NCIt concept]

Position du mot-clé dans l'(les) arborescence(s) :

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