Preferred Name |
Trisomy 21 |
ID |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C43224 |
code |
C43224 |
DEFINITION |
A chromosomal abnormality consisting of the presence of a third copy of chromosome 21 in somatic cells. |
label |
Trisomy 21 |
Legacy_Concept_Name |
Trisomy_21 |
Preferred_Name |
Trisomy 21 |
prefixIRI |
C43224 |
prefLabel |
Trisomy 21 |
Semantic_Type |
Cell or Molecular Dysfunction |
UMLS_CUI |
C3537167 |
subClassOf |