Abnormality of eosinophils
Symptom Information:
Symptom ID: | HPO:0001879 | ||||
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 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) 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) MedDRA: |
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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) |