NANDO ID: 1200347 https://nanbyodata.jp/ontology/NANDO_1200347 Copy
Selective IgA deficiency
Notification number: 65
Overview
Links
Mondo ID | Mondo label (EN) | Match type | Feedback(*) |
---|---|---|---|
MONDO:0001341 | selective IgA deficiency disease | Exact Match |
* Welcome feedback on the links.
MedGen CID | Bridge ID | Mondo label (EN) | Match type | Feedback(*) |
---|---|---|---|---|
C4049006 | MONDO:0001341 | Selective IgA deficiency disease | Exact 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