Monosomy 11 - CISMeF

Preferred Label : Monosomy 11;

NCIt definition : A chromosomal abnormality characterized by the absence of one of the copies of chromosome 11.;

Détails

Origin ID

C36629;

UMLS CUI

C1513477;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 11 [NCIt concept]
may_be_cytogenetic_abnormality_of_disease
- Sporadic Breast Carcinoma [NCIt concept]

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

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