has material basis in germline mutation in CSF3R hereditary disease leukocyte disorder hereditary neutrophilia https://www.malacards.org/card/neutrophilia_hereditary SCTID:129639005 DOID:0090120 OMIM:162830 Orphanet:279943 MESH:C563010 MONDO:0008092 MEDGEN:154252 GARD:0017287 UMLS:C0543669 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.