Eosinophilia

Symptom Information:

Symptom ID: HPO:0001880
Synonyms:
Eosinophil count raised (finding) [Orphanet:48440]
Increased blood eosinophil number (finding) [Orphanet:48440]
Disorder characterized by eosinophilia (disorder) [Orphanet:48440]
Eosinophilia [Orphanet:48440]
Hypereosinophilia [Orphanet:48440]
Eosinophilia [OMIM:Eosinophilia]
Eosinophils anomalies/hypereosinophilia [Orphanet:48440]
Eosinophil count increased [Orphanet:48440]
Eosinophilia [MedDRA:10014950]
Eosinophilia (excl pulmonary) [MedDRA:10014950]
Eosinophilic granulocytosis [MedDRA:10014950]
Hypereosinophilia [MedDRA:10014950]
Eosinophil count increased [MedDRA:10014945]
Blood eosinophils increased [MedDRA:10014945]
Eosinophil count high [MedDRA:10014945]
Plasma eosinophils increased [MedDRA:10014945]
Serum eosinophils increased [MedDRA:10014945]
Hypereosinophilia [OMIM:Hypereosinophilia]
Quality:
Cross references:
Orphanet:48440 "Eosinophils anomalies/hypereosinophilia" [Orphanet:48440]
OMIM: "Eosinophilia" [OMIM:Eosinophilia]
OMIM: "Hypereosinophilia" [OMIM:Hypereosinophilia]
UMLS:C0014457 "Eosinophilia" [HPO:0001880]
UMLS:C0014457 "Eosinophilia" [Orphanet:48440]
UMLS:C2240374 "Eosinophil count raised (finding)" [Orphanet:48440]
UMLS:C0745091 "Hypereosinophilia" [Orphanet:48440]
Is a (Direct Parents):
MedDRA Eosinophilic disorders
HPO         Abnormality of eosinophils
MedDRA White blood cell analyses
HPO         Leukocytosis
Orphanet Abnormality of eosinophils
Orphanet Abnormality of leukocytes
HPO         Eosinophilic fasciitis
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)
             Abnormal leukocyte count(HPO:0011893)
                Leukocytosis(HPO:0001974)
                   Eosinophilia(HPO:0001880)
             Abnormality of myeloid leukocytes(HPO:0010974)
                Abnormality of granulocytes(HPO:0001911)
                   Abnormality of eosinophils(HPO:0001879)
                      Eosinophilia(HPO:0001880)
       Abnormality of the immune system(HPO:0002715)
          Abnormality of cellular immune system(HPO:0010987)
             Abnormality of leukocytes(HPO:0001881)
                Abnormal leukocyte count(HPO:0011893)
                   Leukocytosis(HPO:0001974)
                      Eosinophilia(HPO:0001880)
                Abnormality of myeloid leukocytes(HPO:0010974)
                   Abnormality of granulocytes(HPO:0001911)
                      Abnormality of eosinophils(HPO:0001879)
                         Eosinophilia(HPO:0001880)
MedDRA:
Blood and lymphatic system disorders(MedDRA:10005329)
    Abnormality of leukocytes(HPO:0001881)
       Eosinophilic disorders(MedDRA:10052828)
          Eosinophilia(HPO:0001880)
Investigations(MedDRA:10022891)
    Haematology investigations (incl blood groups)(MedDRA:10018851)
       White blood cell analyses(MedDRA:10047938)
          Eosinophilia(HPO:0001880)
Database Frequency: 35 / 7739
Resource:

All diseases associated with this symptom:

AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME (OMIM:601859)
AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE IIA (OMIM:603909)
Autoimmune lymphoproliferative syndrome (Orphanet:3261)
Autosomal dominant hyper-IgE syndrome (Orphanet:2314)
Autosomal dominant severe congenital neutropenia (Orphanet:486)
Autosomal recessive hyper-IgE syndrome (Orphanet:169446)
Autosomal recessive limb girdle muscular dystrophy type 2A (Orphanet:267)
COMBINED INFLAMMATORY AND IMMUNOLOGIC DEFECT (OMIM:216920)
Cardiomyopathy, familial restrictive, 1 (OMIM:115210)
Combined immunodeficiency due to DOCK8 deficiency (Orphanet:217390)
Congenital cataract-hypertrophic cardiomyopathy-mitochondrial myopathy syndrome (Orphanet:1369)
Desquamative interstitial pneumonia (Orphanet:98852)
EOSINOPHILIA, FAMILIAL (OMIM:131400)
Eosinophilic granulomatosis with polyangiitis (Orphanet:183)
HALOTHANE HEPATITIS (OMIM:234350)
Hereditary mucoepithelial dysplasia (Orphanet:1839)
IMMUNODEFICIENCY 25 (OMIM:610163)
Idiopathic hypereosinophilic syndrome (Orphanet:3260)
Incontinentia pigmenti (Orphanet:464)
Linear and whorled nevoid hypermelanosis (Orphanet:79150)
Loeffler endocarditis (Orphanet:75566)
Lymphoid hypereosinophilic syndrome (Orphanet:314970)
MACROSOMIA ADIPOSA CONGENITA (OMIM:248100)
MYELOPROLIFERATIVE DISORDER, CHRONIC, WITH EOSINOPHILIA (OMIM:131440)
NEUTROPENIA, LETHAL CONGENITAL, WITH EOSINOPHILIA (OMIM:257100)
Neonatal inflammatory skin and bowel disease (Orphanet:294023)
Netherton syndrome (Orphanet:634)
Neutropenia, severe congenital, 1, autosomal dominant (OMIM:202700)
Omenn syndrome (Orphanet:39041)
Primary hypereosinophilic syndrome (Orphanet:314950)
Roifman syndrome (Orphanet:353298)
Severe combined immunodeficiency due to adenosine deaminase deficiency (Orphanet:277)
T-CELL RECEPTOR-ALPHA/BETA DEFICIENCY (OMIM:615387)
Thrombocytopenia - absent radius (Orphanet:3320)
Tropical endomyocardial fibrosis (Orphanet:75565)