Trisomy 15 - CISMeF

Preferred Label : Trisomy 15;

NCIt definition : A chromosomal abnormality consisting of the presence of a third copy of chromosome 15 in somatic cells.;

Details

Origin ID

C84283;

UMLS CUI

C0795856;

Currated CISMeF NLP mapping
- Trisomy 15 [MedDRA Preferred Term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Trisomy 15 [MedDRA Preferred Term]
concept_is_in_subset
- Cellosaurus Disease Terminology [NCIt concept]
- Cellosaurus Terminology [NCIt concept]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 15 [NCIt concept]

Keyword's position in hierarchy(ies) :

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