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Summary Literature (0)
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 : csf3r

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008092 - hereditary neutrophilia

MIM:
MIM:162830 - NEUTROPHILIA, HEREDITARY

Other Model Organisms: Alliance, 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)