inv(16)(p13.3;q24.3)

Preferred Label : inv(16)(p13.3;q24.3);

NCIt synonyms : inv(16)(p13.3q24.3); inv(16)(p13q24); inv(16)(p13;q24);

NCIt definition : A pericentric chromosomal inversion that involves chromosome 16. It is associated with CBFA2T3/GLIS2 fusions and pediatric acute megakaryoblastic leukemia.;

NCI Metathesaurus CUI : CL972422;

Détails

Origin ID

C167195;

UMLS CUI

C5238352;

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]
- CTRP Biomarker Terminology [NCIt concept]
- CTRP Molecular Genetic Biomarker Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 16 [NCIt concept]
molecular_abnormality_involves_gene
- CBFA2T3 Gene [NCIt concept]
- CBFA2T3/GLIS2 Fusion Gene [NCIt concept]
- GLIS2 Gene [NCIt concept]

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

Vous pouvez consulter :

recommendations
documents concerning education
documents for patients