A chromosomal disorder consisting of the presence of two chromosomes of the same type in addition to the normal diploid number. [ https://orcid.org/0000-0002-4142-7153 ]
This is just here as a test because I lose it
Term information
database
cross reference
- MEDGEN:90710 (MONDO:equivalentTo)
- UMLS:C0333689 (MONDO:equivalentTo)
- NCIT:C36601 (MONDO:relatedTo)
- MESH:D058670 (MONDO:equivalentTo)
Subsets
gard_rare, otar, rare
exactMatch
http://identifiers.org/mesh/D058670
http://identifiers.org/medgen/90710
http://linkedlifedata.com/resource/umls/id/C0333689