Preferred Name | Telomere Syndrome | |
Synonyms |
|
|
Definitions |
A group of disorders caused by mutation(s) that disrupt the maintenance of telomeres, resulting in the short telomere defect. |
|
ID |
http://purl.obolibrary.org/obo/NCIT_C152065 |
|
code |
C152065 |
|
Contributing_Source |
CTRP |
|
definition |
A group of disorders caused by mutation(s) that disrupt the maintenance of telomeres, resulting in the short telomere defect. |
|
Display_Name |
Telomere Syndrome |
|
in_subset | ||
label |
Telomere Syndrome |
|
NCI_META_CUI |
CL553398 |
|
Preferred_Name |
Telomere Syndrome |
|
prefixIRI |
NCIT:C152065 |
|
prefLabel |
Telomere Syndrome |
|
Semantic_Type |
Disease or Syndrome |
|
subClassOf |
Create mapping
Delete | Mapping To | Ontology | Source |
---|---|---|---|
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C152065 | NCIT | LOOM | |
http://purl.obolibrary.org/obo/MONDO_0100137 | EFO | LOOM | |
http://purl.obolibrary.org/obo/MONDO_0100137 | MONDO | LOOM | |
http://purl.obolibrary.org/obo/MONDO_0100137 | DOVES | LOOM | |
http://purl.obolibrary.org/obo/MONDO_0100137 | KTAO | LOOM |