Agammaglobulinemia [agamaglobulinemie]

topical
114
Terms

agamaglobulinémie
hypogamaglobulinemie
hypogamaglobulinémie

 

Hypogammaglobulinemia

Persistent link   https://www.medvik.cz/link/D000361
Definition

An immunologic deficiency state characterized by an extremely low level of generally all classes of gamma-globulin in the blood.

Annotation
DYSGAMMAGLOBULINEMIA is also available
DUI
D000361 MeSH Browser
CUI
M0000551

C Diseases
C15.378.147.142 Agammaglobulinemia 114
C15.378.147.333 Dysgammaglobulinemia 10
C15.378.147.542 Hypergammaglobulinemia 55
C15.378.147.607 Hypoproteinemia 27
C15.378.147.780 Paraproteinemias 290
C15.378.147.880 Protein C Deficiency 31
C15.378.147.890 Protein S Deficiency 18
C15.604.515.032 Agammaglobulinemia 114
C15.604.515.245 Castleman Disease 62
C15.604.515.292 Granuloma 236
C15.604.515.435 Heavy Chain Disease 8
C15.604.515.516 Infectious Mononucleosis 191
C15.604.515.553 Leukemia, Hairy Cell 95
C15.604.515.560 Leukemia, Lymphoid 477
C15.604.515.562 Lymphangiomyoma 1
C15.604.515.569 Lymphoma 1 126
C15.604.515.700 Marek Disease 7
C15.604.515.827 Sarcoidosis 501
C15.604.515.841 Sezary Syndrome 43
C15.604.515.880 Tumor Lysis Syndrome 38
C20.673.088 Agammaglobulinemia 114
C20.673.430 Dysgammaglobulinemia 10
C20.673.480 HIV Infections 2 654
C20.673.627 Lymphopenia 45

Achondroplasia and Swiss type agammaglobulinemia Disease MeSH Browser

Agammaglobulinemia, Non-Bruton Type, Autosomal Dominant Disease MeSH Browser

Agammaglobulinemia, X-linked, type 2 Disease MeSH Browser

Agammaglobulinemia, microcephaly, and severe dermatitis Disease MeSH Browser

Agammaglobulinemia, non-Bruton type Disease MeSH Browser

Bruton type agammaglobulinemia Disease MeSH Browser

Frenkel Russe syndrome Disease MeSH Browser

Granulocytopenia with Immunoglobulin Abnormality Disease MeSH Browser

Hypogammaglobulinemia and Isolated growth hormone deficiency, X-linked Disease MeSH Browser

Hypogammaglobulinemia, X-Linked Disease MeSH Browser

Leukoencephalopathy, Arthritis, Colitis, and Hypogammaglobulinema Disease MeSH Browser

Leukoencephalopathy, arthritis, colitis, and hypogammaglobulinemia Disease MeSH Browser

Microcephaly with Chemotactic Defect and Transient Hypogammaglobulinemia Disease MeSH Browser

Osteopetrosis, Autosomal Recessive 7 Disease MeSH Browser

Severe combined immunodeficiency due to adenosine deaminase deficiency Disease MeSH Browser