A rare disorder characterized by recurrent infantile infections and absence of neutrophils in the peripheral blood. [ NCIT:C61242 ]
Synonyms: infantile genetic agranulocytosis congenital neutropenia genetic infantile agranulocytosis
Term information
- GARD:19809 (MONDO:GARD)
- UMLS:C3805116 (MONDO:equivalentTo)
- MEDGEN:1785816 (MONDO:equivalentTo)
- icd11.foundation:87096615 (https://orcid.org/0000-0002-3458-4839)
- ICD10CM:D70 (Orphanet:101987/ntbt)
- NCIT:C61242 (MONDO:equivalentTo)
- Orphanet:101987 (MONDO:equivalentTo)
gard_rare, otar, disease_grouping, rare, ordo_group_of_disorders
http://linkedlifedata.com/resource/umls/id/C3805116
http://identifiers.org/medgen/1785816
http://www.orpha.net/ORDO/Orphanet_101987
http://purl.obolibrary.org/obo/NCIT_C61242