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hereditary neutrophilia

Disease Summary
Associated Targets (1)
Tclin

1


Mondo Description A leukocyte disease characterized by autosomal dominant inheritance of lifelong, persistent elevated neutrophil counts primarily consisting of segmented neutrophils that has material basis in heterozygous mutation in the CSF3R gene on chromosome 1p34.
Uniprot Description A form of lifelong, persistent neutrophilia, a condition characterized by an increase in the number of neutrophils in the blood.
Mondo Term and Equivalent IDs
MONDO:0008092:  hereditary neutrophilia
MESH:C563010: 
Orphanet:279943: 
SCTID:129639005: 
UMLS:C0543669: