Trisomy 16 - CISMeF

Preferred Label : Trisomy 16;

NCIt definition : A chromosomal abnormality consisting of the presence of a third copy of chromosome 16 in somatic cells.;

Details

Origin ID

C37866;

UMLS CUI

C1519651;

Automatic exact mappings (from CISMeF team)
- Chromosome 16, trisomy [MeSH concept]
- Trisomy 16 [MedDRA Preferred Term]
- chromosome 16, trisomy [MeSH Supplementary Concept]
Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
UMLS correspondences (same concept)
- Chromosome 16, trisomy [MeSH concept]
- Mosaic trisomy 16 [ORDO Disease]
- Trisomy 16 [MedDRA Preferred Term]
- chromosome 16, trisomy [MeSH Supplementary Concept]
concept_is_in_subset
- Cellosaurus Disease Terminology [NCIt concept]
- Cellosaurus Terminology [NCIt concept]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 16 [NCIt concept]

Keyword's position in hierarchy(ies) :

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