Synonyms: partial deletion of chromosome type X partial monosomy of chromosome X

This is just here as a test because I lose it

Term information

database cross reference
  • MEDGEN:1826030 (MONDO:equivalentTo)
  • Orphanet:263726 (MONDO:equivalentTo)
  • UMLS:C5679690 (MONDO:equivalentTo)
  • GARD:20911 (MONDO:GARD)
Subsets

gard_rare, disease_grouping, rare, ordo_group_of_disorders

IAO 0000233

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

exactMatch

http://identifiers.org/medgen/1826030

http://linkedlifedata.com/resource/umls/id/C5679690

http://www.orpha.net/ORDO/Orphanet_263726

id

MONDO:0017003