Term info
database cross reference
- MESH:D011123 (Orphanet:96321/e)
- Orphanet:96321 (MONDO:equivalentTo)
- SCTID:72991005 (MONDO:equivalentTo)
Subsets
disease_grouping, ordo_group_of_disorders
definition
Chromosomal disorder in which the chromosomal constitution of a cell containing multiples of the normal number of chromosomes; includes triploidy (symbol: 3N), tetraploidy (symbol: 4N), etc.
exactMatch
http://purl.obolibrary.org/obo/Orphanet_96321, http://identifiers.org/mesh/D011123, http://identifiers.org/snomedct/72991005
id
MONDO:0019934