t(7;12)(q36;p13)

Preferred Label : t(7;12)(q36;p13);

NCIt definition : A chromosomal translocation involving the ETV6 gene on chromosome 12p13 and HLXB9 gene on chromosome 7q36.;

Détails

Origin ID

C122689;

UMLS CUI

C4053813;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
concept_is_in_subset
- AML Authorized Value Terminology [NCIt concept]
- AML Minimal Residual Disease Table [NCIt concept]
- AML Molecular Analysis Table [NCIt concept]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 12 [NCIt concept]
- Human Chromosome 7 [NCIt concept]
is_cytogenetic_abnormality_of_disease
- Acute Myeloid Leukemia with t(7;12)(q36;p13); HLXB9-ETV6 [NCIt concept]
molecular_abnormality_involves_gene
- ETS Family Gene [NCIt concept]
- ETV6 Gene [NCIt concept]
- MNX1 Gene [NCIt concept]
- MNX1/ETV6 Fusion Gene [NCIt concept]

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

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