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Trisomy 21

^ http://purl.obolibrary.org/obo/NCIT_C43224


A chromosomal abnormality consisting of the presence of a third copy of chromosome 21 in somatic cells. [ NCI ]

Synonyms: Trisomy 21

Term info

Subsets

NCIT_C116977, NCIT_C142800, NCIT_C142799

Display Name

Trisomy 21

Legacy Concept Name

Trisomy_21

Preferred Name

Trisomy 21

Semantic Type

Cell or Molecular Dysfunction

UMLS CUI

C3537167

code

C43224