Increased antibody level in blood

Symptom Information:

Symptom ID: HPO:0010702
Synonyms:
Elevated immunoglobulin levels [HPO:0010702]
Hypergammaglobulinaemia [HPO:0010702]
Hyperglobulinemia [HPO:0010702]
Increased gamma globulin [HPO:0010702]
Increased immunoglobulin level [HPO:0010702]
Increased serum gamma globulin [HPO:0010702]
Raised immunoglobulin levels [HPO:0010702]
Hypergammaglobulinemia (finding) [Orphanet:47480]
Hypergammaglobulinemia [Orphanet:47480]
Elevated immunoglobulin levels [OMIM:Elevated immunoglobulin levels]
Hypergammaglobulinemia [OMIM:Hypergammaglobulinemia]
Hyperglobulinemia [OMIM:Hyperglobulinemia]
Raised immunoglobulin levels [OMIM:Raised immunoglobulin levels]
Hypergammaglobulinaemia [Orphanet:47480]
Hypergammaglobulinaemia [MedDRA:10020630]
Gamma globulinaemia [MedDRA:10020630]
Polyclonal hypergammaglobulinaemia [MedDRA:10020630]
Polyclonal hypergammaglobulinemia [MedDRA:10020630]
Hypergammaglobulinemia [MedDRA:10020630]
Gamma globulinemia [MedDRA:10020630]
Polyclonal gammopathy [MedDRA:10020630]
Increased serum gamma-globulin [OMIM:Increased serum gamma-globulin]
Quality:
Cross references:
Orphanet:47480 "Hypergammaglobulinemia" [Orphanet:47480]
OMIM: "Elevated immunoglobulin levels" [OMIM:Elevated immunoglobulin levels]
OMIM: "Hypergammaglobulinemia" [OMIM:Hypergammaglobulinemia]
OMIM: "Hyperglobulinemia" [OMIM:Hyperglobulinemia]
OMIM: "Raised immunoglobulin levels" [OMIM:Raised immunoglobulin levels]
OMIM: "Increased serum gamma-globulin" [OMIM:Increased serum gamma-globulin]
UMLS:C0020455 "Hypergammaglobulinemia" [Orphanet:47480]
Is a (Direct Parents):
Orphanet Abnormality of the immune system
MedDRA Immune and associated conditions NEC
HPO         Abnormal immunoglobulin level
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)
          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)
       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)
MedDRA:
Immune system disorders(MedDRA:10021428)
    Immune disorders NEC(MedDRA:10027665)
       Immune and associated conditions NEC(MedDRA:10027682)
          Increased antibody level in blood(HPO:0010702)
Database Frequency: 29 / 7739
Resource:

All diseases associated with this symptom:

AICARDI-GOUTIERES SYNDROME 7 (OMIM:615846)
Acute interstitial pneumonia (Orphanet:79126)
Autosomal dominant severe congenital neutropenia (Orphanet:486)
CALCIFIC AORTIC DISEASE WITH IMMUNOLOGIC ABNORMALITIES, FAMILIAL (OMIM:114065)
CANDLE syndrome (Orphanet:325004)
CIRRHOSIS, FAMILIAL (OMIM:118900)
Caffey disease (Orphanet:1310)
Gaucher disease (Orphanet:355)
Gaucher disease type 1 (Orphanet:77259)
Gaucher disease type 3 (Orphanet:77261)
HISTIOCYTOSIS, FAMILIAL LIPOCHROME (OMIM:235900)
Idiopathic pulmonary fibrosis (Orphanet:2032)
JMP syndrome (Orphanet:324999)
LYMPHOPENIC HYPERGAMMAGLOBULINEMIA, ANTIBODY DEFICIENCY, AUTOIMMUNEHEMOLYTIC ANEMIA, AND GLOMERULONEPHRITIS (OMIM:247800)
Lymphoid interstitial pneumonia (Orphanet:79128)
NEUTROPENIA, CHRONIC FAMILIAL (OMIM:162700)
Nakajo-Nishimura syndrome (Orphanet:2615)
Neonatal hemochromatosis (Orphanet:446)
Neutropenia, severe congenital, 1, autosomal dominant (OMIM:202700)
Polyarteritis nodosa, childhood-onset (OMIM:615688)
Proteasome disability syndrome (Orphanet:324977)
Pulmonary nodular lymphoid hyperplasia (Orphanet:60026)
RAS-ASSOCIATED AUTOIMMUNE LEUKOPROLIFERATIVE DISORDER (OMIM:614470)
Recurrent infections-myelofibrosis-nephromegaly syndrome (Orphanet:369852)
SARCOIDOSIS, SUSCEPTIBILITY TO, 1 (OMIM:181000)
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 1 (OMIM:606002)
STING-ASSOCIATED VASCULOPATHY, INFANTILE-ONSET (OMIM:615934)
Sarcoidosis (Orphanet:797)
Spinocerebellar ataxia with axonal neuropathy type 2 (Orphanet:64753)