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
This is just here as a test because I lose it
Term information
database
cross reference
- NCIT:C61242 (MONDO:equivalentTo)
- GARD:19809 (Orphanet:101987)
- ICD10CM:D70 (Orphanet:101987/ntbt)
- Orphanet:101987 (MONDO:equivalentTo)
Subsets
gard_rare, disease_grouping, rare, orphanet_rare, ordo_group_of_disorders