Disease #01469 (neutrophilia, hereditary, OMIM:162830)

Official abbreviation -
Name neutrophilia, hereditary
OMIM ID 162830
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene CSF3R
Associated tissues -
Disease features -
Remarks -