A chromosomal abnormality consisting of the presence of a third copy of chromosome 8 in somatic cells. [ NCIT:C36396 ]
This is just here as a test because I lose it
Term information
database
cross reference
- SCTID:205649008 (MONDO:equivalentTo)
- NCIT:C36396 (MONDO:relatedTo)
- MEDGEN:98158 (MONDO:equivalentTo)
- MESH:C537942 (MONDO:equivalentTo)
- UMLS:C0432412 (MONDO:equivalentTo)
Subsets
gard_rare, otar, rare
exactMatch
http://identifiers.org/mesh/C537942
http://identifiers.org/snomedct/205649008
http://identifiers.org/medgen/98158
http://linkedlifedata.com/resource/umls/id/C0432412