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)
- MESH:C537942 (MONDO:equivalentTo)
- NCIT:C36396 (MONDO:equivalentTo)
definition
A chromosomal abnormality consisting of the presence of a third copy of chromosome 8 in somatic cells.
exactMatch
http://identifiers.org/mesh/C537942
http://identifiers.org/snomedct/205649008
http://purl.obolibrary.org/obo/NCIT_C36396