Synonyms: partial monosomy of chromosome 10

This is just here as a test because I lose it

Term information

database cross reference
  • Orphanet:261811 (MONDO:equivalentTo)
  • MEDGEN:1826016 (MONDO:equivalentTo)
  • GARD:20798 (MONDO:GARD)
  • UMLS:C5679658 (MONDO:equivalentTo)
Subsets

gard_rare, disease_grouping, rare, ordo_group_of_disorders

IAO 0000233

https://github.com/monarch-initiative/mondo/issues/3664

exactMatch

http://linkedlifedata.com/resource/umls/id/C5679658

http://www.orpha.net/ORDO/Orphanet_261811

http://identifiers.org/medgen/1826016

id

MONDO:0016875