NANDO ID: 1200347 https://nanbyodata.jp/ontology/NANDO_1200347 Copy

Selective IgA deficiency

Overview

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MONDO:0001341selective IgA deficiency diseaseExact Match

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MedGen CIDBridge IDMondo label (EN)Match typeFeedback(*)
C4049006MONDO:0001341Selective IgA deficiency diseaseExact Match
Descriptions
A dysgammaglobulinemia characterized by low or undetectable serum levels of immunoglobulin class A (IgA). It is the most common primary antibody deficiency. It may be inherited or the reversible sequela of infection or certain drugs. It may be caused by decreased or inefficient class-switching from progenitor B cells without any corresponding decreases in the other isotypes. Though affected persons may be asymptomatic, low levels of IgA will reduce the immune system's ability to combat infection where IgA is normally secreted, at mucosal surfaces. Selective IgA deficiency is seen in greater proportion among patients with autoimmune disorders. >> 翻訳 (Google)
A dysgammaglobulinemia characterized by low or undetectable serum levels of immunoglobulin class A (IgA). It is the most common primary antibody deficiency. It may be inherited or the reversible sequela of infection or certain drugs. It may be caused by decreased or inefficient class-switching from progenitor B cells without any corresponding decreases in the other isotypes. Though affected persons may be asymptomatic, low levels of IgA will reduce the immune system''s ability to combat infection where IgA is normally secreted, at mucosal surfaces. Selective IgA deficiency is seen in greater proportion among patients with autoimmune disorders. >> 翻訳 (Google)
Synonyms
EN
deficiencies, IgA
deficiency, IgA
gamma-A-globulin deficiency
IgA deficiencies
IgA deficiency
immunoglobulin A deficiency
immunoglobulin alpha deficiency
selective IgA deficiency disease
selective IgA immunodeficiency
selective immunoglobulin A deficiency
SIgAD