OBO ID: DOID:0090120
Term Name: hereditary neutrophilia Search Ontology:
Synonyms:
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. (2)
References:
Ontology: Human Disease   ( DOID:0090120 )
Relationships
is a type of:
OTHER hereditary neutrophilia PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
CSF3R ?Neutrophilia, hereditary 162830
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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