hereditary neutrophilia

Summary
Definition
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 colony stimulating factor 3 receptor (CSF3R) gene on chromosome 1p34.
Super Class
autosomal dominant disease leukocyte disease
Disease Ontology
DOID:0090120
Mondo Disease Ontology
MeSH
UMLS
ORDO
OMIM
MGI genotype (from TogoID)
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
1441 CSF3R colony stimulating factor 3 receptor
Displaying 1 entry
Gene ID Gene Symbol Description Source
12986 Csf3r colony stimulating factor 3 receptor

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024