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Echinobase
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 CSF3R gene on chromosome 1p34.

Synonyms:

Echinobase Genes :


OMIM:
MIM:162830 - neutrophilia, hereditary

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): leukocyte disease (is_a)