ID: 59

Disease Name: Agammaglobulinemia

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

Disease Type: Clinical conditions associated with amyloidosis

ICD-10 Classification: Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism

Tissue: Kidney, Gastrointestinal Tract, Spleen, Liver

Cross References
http://apps.who.int/classifications/icd10/browse/2016/en#/D80

https://meshb.nlm.nih.gov/record/ui?ui=D000361

https://www.ncbi.nlm.nih.gov/pubmed/14194996

https://www.ncbi.nlm.nih.gov/pubmed/24292696

https://www.ncbi.nlm.nih.gov/pubmed/8810937

Alternative Names:
Agammaglobulinemia
Agammaglobulinemia, BTK
Agammaglobulinemia, Bruton tyrosine kinase
Agammaglobulinemia, X-Linked
Agammaglobulinemia, X-Linked, Type I
Bruton's Agammaglobulinemia
Bruton-Type Agammaglobulinemia
Bruton-type (congenital X-linked) agammaglobulinemia
Congenital Agammaglobulinemia
Immunodeficiency 1
X-linked agammaglobulinemia
Hypogammaglobulinemia 

Precursor Proteins:
P0DJI8 | Serum amyloid A-1 protein
P0DJI9 | Serum amyloid A-2 protein


Co-deposited Proteins:
No information available



Link to Amyloidosis: 
	http://83.212.109.111:8084/amyco/29

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