t(1;22) - CISMeF

Preferred Label : t(1;22);

NCIt definition : A cytogenetic abnormality that involves a translocation between chromosomes 1 and 22.;

NCI Metathesaurus CUI : CL1412945;

Détails

Origin ID

C175584;

UMLS CUI

C5446638;

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 1 [NCIt concept]
- Human Chromosome 22 [NCIt concept]

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

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