Abnormality of eosinophils

Symptom Information:

Symptom ID: HPO:0001879
Synonyms:
Eosinophils anomaly [Orphanet:48440]
Eosinophils anomalies/hypereosinophilia [Orphanet:48440]
Quality:
Cross references:
Orphanet:48440 "Eosinophils anomalies/hypereosinophilia" [Orphanet:48440]
Is a (Direct Parents):
Orphanet Abnormality of leukocytes
HPO         Abnormality of granulocytes
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       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 eosinophils(HPO:0001879)
       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 eosinophils(HPO:0001879)
MedDRA:
Database Frequency: 20 / 7739
Resource:

All diseases associated with this symptom:

Aggressive systemic mastocytosis (Orphanet:98850)
Allergic bronchopulmonary aspergillosis (Orphanet:1164)
Anisakiasis (Orphanet:1070)
Autosomal dominant hyper-IgE syndrome (Orphanet:2314)
Cyclic neutropenia (Orphanet:2686)
Dermatomyositis (Orphanet:221)
Distomatosis (Orphanet:1685)
Drug rash with eosinophilia and systemic symptoms (Orphanet:139402)
EOSINOPHIL PEROXIDASE DEFICIENCY (OMIM:261500)
Eosinophilic fasciitis (Orphanet:3165)
Eosinophilic granulomatosis with polyangiitis (Orphanet:183)
Hereditary folate malabsorption (Orphanet:90045)
Hydatidosis (Orphanet:400)
Idiopathic acute eosinophilic pneumonia (Orphanet:724)
Incontinentia pigmenti (Orphanet:464)
Myalgia-eosinophilia syndrome associated with tryptophan (Orphanet:2582)
Omenn syndrome (Orphanet:39041)
Systemic mastocytosis (Orphanet:2467)
Systemic mastocytosis with an associated clonal hematologic non-mast cell lineage disease (Orphanet:98849)
Wells syndrome (Orphanet:901)