Eosinophilia
Symptom Information:
Symptom ID: | HPO:0001880 | ||||||||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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) |
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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) |