Synonyms: deletion 22 Del(22) monosomy type 22
This is just here as a test because I lose it
Term information
database
cross reference
- GARD:19324 (MONDO:GARD)
- UMLS:C0795878 (MONDO:equivalentTo)
- Orphanet:96123 (MONDO:equivalentTo)
- NCIT:C36461 (MONDO:relatedTo)
- MEDGEN:208644 (MONDO:equivalentTo)
Subsets
gard_rare, ordo_disorder, otar, rare, ordo_malformation_syndrome, nord_rare, orphanet_rare
exactMatch
http://identifiers.org/medgen/208644
http://linkedlifedata.com/resource/umls/id/C0795878
http://www.orpha.net/ORDO/Orphanet_96123