del(9p21) - CISMeF

Preferred Label : del(9p21);

NCIt definition : A cytogenetic abnormality that refers to any loss of genetic material from the short arm of chromosome 9 that includes the band at 9p21.;

NCI Metathesaurus CUI : CL1643056;

Details

Origin ID

C177307;

UMLS CUI

C5447684;

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 9 [NCIt concept]
may_be_cytogenetic_abnormality_of_disease
- Melanoma-Astrocytoma Syndrome [NCIt concept]

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