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
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