autosomal recessive severe congenital neutropenia due to CXCR2 deficiency
http://purl.obolibrary.org/obo/MONDO_0018487
Term info
database cross reference
- Orphanet:420699 (MONDO:equivalentTo)
Subsets
ordo_disease
exactMatch
http://purl.obolibrary.org/obo/Orphanet_420699
id
MONDO:0018487