A chromosomal abnormality consisting of the presence of one chromosome in addition to the normal diploid number. [ NCIT:C3421 ]
This is just here as a test because I lose it
Term information
database
cross reference
- MESH:D014314 (https://orcid.org/0000-0003-1967-3726)
- UMLS:C0041107 (MONDO:equivalentTo)
- NCIT:C3421 (MONDO:relatedTo)
- MEDGEN:21702 (MONDO:equivalentTo)
Subsets
gard_rare, otar, rare
exactMatch
http://linkedlifedata.com/resource/umls/id/C0041107
http://identifiers.org/mesh/D014314
http://identifiers.org/medgen/21702