Increased IgE level

Symptom Information:

Symptom ID: HPO:0003212
Synonyms:
Elevated immunoglobulin E [HPO:0003212]
Elevated serum IgE [HPO:0003212]
High immunoglobulin E [HPO:0003212]
Elevated serum IgE [OMIM:Elevated serum IgE]
Elevated immunoglobulin E (IgE) [OMIM:Elevated immunoglobulin E (IgE)]
Increased IgE levels [OMIM:Increased IgE levels]
Quality:
Cross references:
OMIM: "Elevated serum IgE" [OMIM:Elevated serum IgE]
OMIM: "Elevated immunoglobulin E (IgE)" [OMIM:Elevated immunoglobulin E (IgE)]
OMIM: "Increased IgE levels" [OMIM:Increased IgE levels]
Is a (Direct Parents):
HPO         Increased antibody level in blood
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 lymphocytes(HPO:0004332)
                   Abnormality of B cells(HPO:0002846)
                      Abnormality of B cell physiology(HPO:0005372)
                         Abnormal immunoglobulin level(HPO:0010701)
                            Increased antibody level in blood(HPO:0010702)
                               Increased IgE level(HPO:0003212)
          Abnormality of immune system physiology(HPO:0010978)
             Abnormality of humoral immunity(HPO:0005368)
                Abnormal immunoglobulin level(HPO:0010701)
                   Increased antibody level in blood(HPO:0010702)
                      Increased IgE level(HPO:0003212)
       Abnormality of blood and blood-forming tissues(HPO:0001871)
          Abnormality of leukocytes(HPO:0001881)
             Abnormality of lymphocytes(HPO:0004332)
                Abnormality of B cells(HPO:0002846)
                   Abnormality of B cell physiology(HPO:0005372)
                      Abnormal immunoglobulin level(HPO:0010701)
                         Increased antibody level in blood(HPO:0010702)
                            Increased IgE level(HPO:0003212)
MedDRA:
Database Frequency: 13 / 7739
Resource:

All diseases associated with this symptom:

Autosomal dominant hyper-IgE syndrome (Orphanet:2314)
Autosomal recessive hyper-IgE syndrome due to TYK2 deficiency (Orphanet:331226)
DEAFNESS, NEURAL, WITH ATYPICAL ATOPIC DERMATITIS (OMIM:221700)
Desquamative interstitial pneumonia (Orphanet:98852)
Epidermolytic palmoplantar keratoderma (Orphanet:2199)
Generalized peeling skin syndrome (Orphanet:263543)
IgE RESPONSIVENESS, ATOPIC (OMIM:147050)
Lymphoid hypereosinophilic syndrome (Orphanet:314970)
Netherton syndrome (Orphanet:634)
Severe combined immunodeficiency due to adenosine deaminase deficiency (Orphanet:277)
WISKOTT-ALDRICH SYNDROME (OMIM:301000)
WISKOTT-ALDRICH SYNDROME, AUTOSOMAL DOMINANT FORM (OMIM:600903)
X-linked thrombocytopenia with normal platelets (Orphanet:852)