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Agammaglobulinemia
MeSH Descriptor Data 2024
Details
Qualifiers
MeSH Tree Structures
Concepts
MeSH Heading
Agammaglobulinemia
Tree Number(s)
C15.378.147.142
C15.604.515.032
C20.673.088
Unique ID
D000361
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D000361
Annotation
DYSGAMMAGLOBULINEMIA
is also available
Scope Note
An immunologic deficiency state characterized by an extremely low level of generally all classes of gamma-globulin in the blood.
Entry Term(s)
Hypogammaglobulinemia
NLM Classification #
WH 400
See Also
Protein-Losing Enteropathies
Date Established
1966/01/01
Date of Entry
1999/01/01
Revision Date
2013/07/08
Allowable Qualifiers
blood (BL)
cerebrospinal fluid (CF)
chemically induced (CI)
classification (CL)
complications (CO)
congenital (CN)
diagnosis (DI)
diagnostic imaging (DG)
diet therapy (DH)
drug therapy (DT)
economics (EC)
embryology (EM)
enzymology (EN)
epidemiology (EP)
ethnology (EH)
etiology (ET)
genetics (GE)
history (HI)
immunology (IM)
metabolism (ME)
microbiology (MI)
mortality (MO)
nursing (NU)
parasitology (PS)
pathology (PA)
physiopathology (PP)
prevention & control (PC)
psychology (PX)
radiotherapy (RT)
rehabilitation (RH)
surgery (SU)
therapy (TH)
urine (UR)
veterinary (VE)
virology (VI)
Hemic and Lymphatic Diseases [C15]
Hematologic Diseases [C15.378]
Blood Protein Disorders [C15.378.147]
Agammaglobulinemia [C15.378.147.142]
Antithrombin III Deficiency [C15.378.147.150]
Dysgammaglobulinemia [C15.378.147.333]
Hypergammaglobulinemia [C15.378.147.542]
Hypoproteinemia [C15.378.147.607]
Paraproteinemias [C15.378.147.780]
Protein C Deficiency [C15.378.147.880]
Protein S Deficiency [C15.378.147.890]
Hemic and Lymphatic Diseases [C15]
Lymphatic Diseases [C15.604]
Lymphoproliferative Disorders [C15.604.515]
Agammaglobulinemia [C15.604.515.032]
Autoimmune Lymphoproliferative Syndrome [C15.604.515.138]
Castleman Disease [C15.604.515.245]
Granuloma [C15.604.515.292]
Heavy Chain Disease [C15.604.515.435]
Immunoblastic Lymphadenopathy [C15.604.515.509]
Infectious Mononucleosis [C15.604.515.516]
Leukemia, Hairy Cell [C15.604.515.553]
Leukemia, Lymphoid [C15.604.515.560]
Lymphangiomyoma [C15.604.515.562]
Lymphoma [C15.604.515.569]
Marek Disease [C15.604.515.700]
Sarcoidosis [C15.604.515.827]
Sezary Syndrome [C15.604.515.841]
Tumor Lysis Syndrome [C15.604.515.880]
Waldenstrom Macroglobulinemia [C15.604.515.925]
Immune System Diseases [C20]
Immunologic Deficiency Syndromes [C20.673]
Agammaglobulinemia [C20.673.088]
Common Variable Immunodeficiency [C20.673.330]
Dysgammaglobulinemia [C20.673.430]
HIV Infections [C20.673.480]
Deltaretrovirus Infections [C20.673.483]
Lymphopenia [C20.673.627]
Phagocyte Bactericidal Dysfunction [C20.673.774]
Primary Immunodeficiency Diseases [C20.673.795]
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Agammaglobulinemia
Preferred
Concept UI
M0000551
Scope Note
An immunologic deficiency state characterized by an extremely low level of generally all classes of gamma-globulin in the blood.
Terms
Agammaglobulinemia
Preferred Term
Term UI
T001153
Date
01/01/1999
LexicalTag
NON
ThesaurusID
Hypogammaglobulinemia
Related
Concept UI
M0000552
Terms
Hypogammaglobulinemia
Preferred Term
Term UI
T001154
Date
06/16/1977
LexicalTag
NON
ThesaurusID
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