homozygous 2p21 microdeletion syndrome
http://purl.obolibrary.org/obo/MONDO_0018246
Term info
database cross reference
- Orphanet:369886 (MONDO:equivalentTo)
- UMLS:CN204808 (MONDO:equivalentTo)
Subsets
disease_grouping, ordo_group_of_disorders
IAO 0000233
https://github.com/monarch-initiative/mondo/issues/3664
exactMatch
http://linkedlifedata.com/resource/umls/id/CN204808, http://purl.obolibrary.org/obo/Orphanet_369886
has exact synonym
2p21 contiguous gene deletion syndrome
id
MONDO:0018246