Synonyms: neutropenia, severe congenital SCN

This is just here as a test because I lose it

Term information

database cross reference
  • NCIT:C166152 (MONDO:equivalentTo)
  • SCTID:89655007 (MONDO:equivalentTo)
  • NORD:1705 (MONDO:NORD)
  • GARD:13592 (Orphanet:42738)
  • DOID:0050590 (MONDO:equivalentTo)
  • Orphanet:42738 (MONDO:equivalentTo)
  • MedDRA:10052210 (Orphanet:42738/e)
  • OMIMPS:202700 (MONDO:equivalentTo)
  • ICD9:288.01 (MONDO:i2s)
Subsets

gard_rare, disease_grouping, rare, nord_rare, orphanet_rare, ordo_group_of_disorders

IAO 0000233

https://github.com/monarch-initiative/mondo/issues/4069

closeMatch

http://identifiers.org/meddra/10052210

exactMatch

http://purl.obolibrary.org/obo/NCIT_C166152

https://omim.org/phenotypicSeries/PS202700

http://www.orpha.net/ORDO/Orphanet_42738

http://purl.obolibrary.org/obo/DOID_0050590

http://identifiers.org/snomedct/89655007

id

MONDO:0018542

Term relations