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DO Term : hereditary neutrophilia [DOID:0090120] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  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:
  • ORDO:279943,
  • 162830,
  • SNOMEDCT_US_2023_03_01:129639005,
  • UMLS_CUI:C0543669,
  • MESH:C563010,
  • OMIM:162830
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Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents