hereditary neutrophilia

Summary

DOID:0090120 - hereditary neutrophilia

Disease Ontology 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.

Synonyms:

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: csf3r

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0008092 - hereditary neutrophilia

MONDO:0008092 - hereditary neutrophilia

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal dominant disease (is_a), leukocyte disease (is_a)