A chromosomal abnormality consisting of the absence of one chromosome from the normal diploid number. [ NCIT:C3239 ]
This is just here as a test because I lose it
Term information
database
cross reference
- MEDGEN:6432 (MONDO:equivalentTo)
- MESH:D009006 (MONDO:equivalentTo)
- UMLS:C0026499 (MONDO:equivalentTo)
- NCIT:C3239 (MONDO:relatedTo)
Subsets
gard_rare, otar, rare
exactMatch
http://identifiers.org/medgen/6432
http://identifiers.org/mesh/D009006
http://linkedlifedata.com/resource/umls/id/C0026499