Increased antibody level in blood
Symptom Information:
Symptom ID: | HPO:0010702 | ||||||||||||||||||||||
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 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) |
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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) |