Preferred Name |
Trisomy 21 |
|
Synonyms |
|
|
Definitions |
A chromosomal abnormality consisting of the presence of a third copy of chromosome 21 in somatic cells. |
|
ID |
http://purl.obolibrary.org/obo/NCIT_C43224 |
|
ALT_DEFINITION |
A chromosomal abnormality consisting of the presence of part or all of a third copy of chromosome 21 in somatic cells. |
|
code |
C43224 |
|
Contributing_Source |
Cellosaurus ACC/AHA CTRP PCDC |
|
definition |
A chromosomal abnormality consisting of the presence of a third copy of chromosome 21 in somatic cells. |
|
Display_Name |
Trisomy 21 |
|
in_subset |
http://purl.obolibrary.org/obo/NCIT_C178115 http://purl.obolibrary.org/obo/NCIT_C178102 http://purl.obolibrary.org/obo/NCIT_C174019 http://purl.obolibrary.org/obo/NCIT_C116977 http://purl.obolibrary.org/obo/NCIT_C173201 http://purl.obolibrary.org/obo/NCIT_C165258 http://purl.obolibrary.org/obo/NCIT_C167409 |
|
Is_PCDC_ALL_Permissible_Value_For_Variable | ||
Is_PCDC_AML_Permissible_Value_For_Variable | ||
label |
Trisomy 21 |
|
Legacy Concept Name |
Trisomy_21 |
|
Preferred_Name |
Trisomy 21 |
|
prefixIRI |
NCIT:C43224 |
|
prefLabel |
Trisomy 21 |
|
Semantic_Type |
Cell or Molecular Dysfunction |
|
UMLS_CUI |
C3537167 |
|
subClassOf |