del(11p15.5) - CISMeF

Preferred Label : del(11p15.5);

NCIt definition : A cytogenetic abnormality that refers to any loss of genetic material from the short arm of chromosome 11 that includes the band at 11p15.5.;

NCI Metathesaurus CUI : CL1643057;

Détails

Origin ID

C177306;

UMLS CUI

C5447683;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
concept_is_in_subset
- CCPS Genetics Terminology [NCIt concept]
- Childhood Cancer Predisposition Study Terminology [NCIt concept]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 11 [NCIt concept]
may_be_cytogenetic_abnormality_of_disease
- Beckwith-Wiedemann Syndrome [NCIt concept]

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