Neutrophillia

Symptom Information:

Symptom ID: HPO:0011897
Synonyms:
Neutrophilia [Orphanet:48480]
Neutrophilia (disorder) [Orphanet:48480]
Neutrophilia (finding) [Orphanet:48480]
Polynuclear cells/neutrophils anomalies/neutropenia [Orphanet:48480]
Neutrophilia [MedDRA:10029379]
Neutrophilia [OMIM:Neutrophilia]
Quality:
Cross references:
Orphanet:48480 "Polynuclear cells/neutrophils anomalies/neutropenia" [Orphanet:48480]
OMIM: "Neutrophilia" [OMIM:Neutrophilia]
UMLS:C0151683 "Neutrophilia" [Orphanet:48480]
Is a (Direct Parents):
HPO         Abnormal neutrophil cell number
Orphanet Abnormality of neutrophils
MedDRA Leukocytoses NEC
Orphanet Abnormality of leukocytes
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the immune system(HPO:0002715)
          Abnormality of cellular immune system(HPO:0010987)
             Abnormality of leukocytes(HPO:0001881)
                Abnormality of myeloid leukocytes(HPO:0010974)
                   Abnormality of granulocytes(HPO:0001911)
                      Abnormality of neutrophils(HPO:0001874)
                         Abnormal neutrophil cell number(HPO:0011991)
                            Neutrophillia(HPO:0011897)
       Abnormality of blood and blood-forming tissues(HPO:0001871)
          Abnormality of leukocytes(HPO:0001881)
             Abnormality of myeloid leukocytes(HPO:0010974)
                Abnormality of granulocytes(HPO:0001911)
                   Abnormality of neutrophils(HPO:0001874)
                      Abnormal neutrophil cell number(HPO:0011991)
                         Neutrophillia(HPO:0011897)
MedDRA:
Blood and lymphatic system disorders(MedDRA:10005329)
    Abnormality of leukocytes(HPO:0001881)
       Leukocytoses NEC(MedDRA:10024379)
          Neutrophillia(HPO:0011897)
Database Frequency: 4 / 7739
Resource:

All diseases associated with this symptom:

Familial isolated dilated cardiomyopathy (Orphanet:154)
Hereditary neutrophilia (Orphanet:279943)
Hyperimmunoglobulinemia D with periodic fever (Orphanet:343)
Wolcott-Rallison syndrome (Orphanet:1667)