Term info
database cross reference
- Orphanet:42738 (MONDO:equivalentTo)
- ICD9:288.01 (MONDO:i2s)
- MedDRA:10052210 (Orphanet:42738/e)
- OMIMPS:202700 (MONDO:equivalentTo)
- SCTID:89655007 (MONDO:equivalentTo)
- DOID:0050590 (MONDO:equivalentTo)
- NCIT:C166152 (MONDO:equivalentTo)
Subsets
disease_grouping, 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, http://purl.obolibrary.org/obo/Orphanet_42738, https://omim.org/phenotypicSeries/PS202700, http://purl.obolibrary.org/obo/DOID_0050590, http://identifiers.org/snomedct/89655007
has exact synonym
neutropenia, severe congenital, SCN
id
MONDO:0018542