Agent Commons Collaborative Research
Hereditary neutrophilia
rareA 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.
- Identifiers
- MONDO:0008092 OMIM:162830Orphanet:279943
- Causal genes
- CSF3R
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